L-aspartic acid

L-aspartic acid structural formula

Structural formula

Business number 017Y
Molecular formula C4H7NO4
Molecular weight 133.1
label

L(+)-aminosuccinic acid,

L(+)-aminosuccinic acid,

L-aspartic acid,

L-aspartic acid,

(S)-(+)-Aminosuccinic acid,

(S)-Aspartic acid,

biochemical reagents,

Intermediates

Numbering system

CAS number:56-84-8

MDL number:MFCD00002616

EINECS number:200-291-6

RTECS number:CI9098500

BRN number:1723530

PubChem ID:None

Physical property data

1. Properties: Colorless orthorhombic leaf-shaped or rod-shaped crystals or crystalline powder, odorless. Often left-handed optical rotation.

2. Density (g/mL, 25/4℃): (d12.5/4) 1.514

3. Relative vapor density (g/mL, air=1) : Undetermined

4. Melting point (ºC): 270-271

5. Boiling point (ºC, normal pressure): Undetermined

6. Boiling point ( ºC, 5.2kPa): Not determined

7. Refractive index: Not determined

8. Flash point (ºC): Not determined

9. Specific optical rotation Degree (º): [a]20/D+25° (c=1.97, in 6mol/L hydrochloric acid).

10. Autoignition point or ignition temperature (ºC): Undetermined

11. Vapor pressure (kPa, 25ºC): Undetermined

12. Saturation Vapor pressure (kPa, 60ºC): Undetermined

13. Heat of combustion (KJ/mol): Undetermined

14. Critical temperature (ºC): Undetermined

15. Critical pressure (KPa): Undetermined

16. Log value of oil-water (octanol/water) partition coefficient: Undetermined

17. Explosion upper limit (% , V/V): Undetermined

18. Lower explosion limit (%, V/V): Undetermined

19. Solubility: soluble in hot water, acid, alkali and Salt solution, insoluble in ethanol and ether.

Toxicological data

1. Acute toxicity: mouse abdominal LC50: 6mg/kg

2. Other multiple dose toxicity: rat oral TDLo: 25079mg/kg/7D-C

3. Mutagenicity: sister chromatids exchangeTEST system: human lymphocytes: 10mg/L

Ecological data

None

Molecular structure data

1. Molar refractive index: 27.20

2. Molar volume (cm3/mol): 87.8

3. Isotonic specific volume (90.2K ): 261.3

4. Surface tension (dyne/cm): 78.2

5. Polarizability (10-24cm3): 10.78

Compute chemical data

1. Reference value for hydrophobic parameter calculation (XlogP): None

2. Number of hydrogen bond donors: 3

3. Number of hydrogen bond acceptors: 5

4. Number of rotatable chemical bonds: 3

5. Number of tautomers: none

6. Topological molecule polar surface area 101

7. Number of heavy atoms: 9

8. Surface charge: 0

9. Complexity: 133

10. Number of isotope atoms: 0

11. Determine the number of atomic stereocenters: 1

12. Uncertain number of atomic stereocenters: 0

13. Determine the number of chemical bond stereocenters: 0

14. Number of uncertain chemical bond stereocenters: 0

15. Number of covalent bond units: 1

Properties and stability

1. Stable properties under normal temperature and pressure.

2. It is a natural product and non-toxic.

3. Exist in tobacco leaves and smoke.

Storage method

Seal and store in a dry place.

Synthesis method

1. The preparation methods of L-aspartic acid include synthesis method and fermentation method. 1. The synthesis method mainly uses maleic acid or fumaric acid or their esters as raw materials, which are treated with ammonia under pressure and then hydrolyzed. It is relatively easy to synthesize racemic aspartic acid, but so far there is no ideal method to separate the racemate. 2. In the fermentation method, fumaric acid and ammonia are added under the action of enzymes to obtain products with high yields. This method only generates the left-handed form with high yield, so it is the main method for industrial production.

2. Obtained from fumaric acid and ammonia under the action of aspartase of Pseudomonas clover or Brevibacterium ammoniagenes.

3. Use maleic acid, fumaric acid or their esters as raw materials, and add ammonia under the action of enzymes. The reaction is as follows:

4. Tobacco: BU, 22; FC, 21.

Purpose

1. Biochemical and medical clinical research. It can be used as an ammonia detoxifier, liver function promoter, fatigue recovery agent and other pharmaceuticals. It can be used to make L-sodium aspartate food additives and additives for various refreshing drinks. It can also be used as biochemical reagents, culture media and organic synthesis intermediates.

2. Can be used as biochemical reagents, culture media and organic synthesis intermediates. In medicine, it is used as a component of heart disease drugs, liver function promoters, ammonia detoxifiers, fatigue relievers and amino acid infusions. It is also used as a preservative in the food industry.

3. Nutritional supplements. Add to various refreshing drinks. It is used medicinally as an ammonia detoxifier and liver function promoter. Used as nutritional additive in cosmetics.

4. L-aspartic acid is often used as a chiral substrate in diastereomeric alkylation reactions, and can be used as a chiral source to synthesize other chiral compounds.

Diastereoselective alkylation L-aspartate ester can be used in α– and β– Alkylation occurs (formula 1) [2], among which the β-alkylation reaction is the most widely used. During the β-alkylation reaction, the amino acid moiety has an important influence on the diastereoselectivity of the reaction. At the same time, β-dicarbonyl compounds can also be prepared through β-alkylation of cyclic derivatives of L-aspartic acid [3].

Synthesis of Chiral Compounds Using L-aspartic acid as the chiral source, a series of chiral compounds can be synthesized, such as using copper iodide After the action of sodium borohydride, etc., a multifunctional oxygen nitrogen heterocyclic compound (formula 2) can be obtained, which can further generate a quinoline compound [4].

Formation of amide bond L-aspartic acid, as an amino acid, is the same as other amino acids Amide compounds (formula 3)[5] can also be generated.

At the same time, you can also use L- Aspartic acid is used as the parent to realize the synthesis of cyclic lactam. For example, the synthesis of six-membered ring lactam (formula 4)[6]. The alkoxy group is also present in the product and therefore serves as an additional reaction site for further derivatization.

β Synthesis of amino acids (or amino acid esters) L-aspartic acid can generate β-amino acids or amino acid esters ( Formula 5)[10], this reaction realizes the conversion from natural amino acids to unnatural amino acids.

In addition, the L-aspartic acid molecule contains two carboxyl groups and one amino group, so it can be used as a multidentate ligand to coordinate with metal ions[7~9] Or form lactone compounds themselves[10,11].

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2,5-Dimethyl-1-phenylpyrrole

2,5-dimethyl-1-phenylpyrrole structural formula

Structural formula

Business number 01TG
Molecular formula C12H13N
Molecular weight 171.24
label

1-phenyl-2,5-dimethylpyrrole,

2,5-Dimethyl-1-phenyl-1H-pyrrole,

1-Phenyl-2,5-dimethylpyrrole

Numbering system

CAS number:83-24-9

MDL number:MFCD00022464

EINECS number:201-461-2

RTECS number:None

BRN number:124370

PubChem ID:None

Physical property data

1. Physical property data


1. Character: Uncertain


2. Density (g/mL,25/4℃): Unsure


3. Relative vapor density (g/ mL,air=1 ): Unsure


4. Melting point (ºC):50-51


5. Boiling point (ºC,Normal pressure):155-160


6. Boiling point (ºC,5.2kPa): Unsure


7. Refractive index: Uncertain


8. Flash Point (ºC): Unsure


9. Specific optical rotation (º): Unsure


10. Autoignition point or ignition temperature (ºC): Unsure


11. Vapor pressure (kPa,25ºC): Unsure


12. Saturation vapor pressure (kPa,60ºC): Unsure


13. Heat of combustion (KJ/mol): Unsure


14. Critical temperature (ºC): Unsure


15. Critical pressure (KPa): Unsure


16. Oil and water (octanol/Log value of the partition coefficient (water): Uncertain


17. Explosion limit ( %,V/V): Unsure


18. Lower explosion limit (%,V/V): Unsure


19. Solubility: Uncertain.

Toxicological data

None

Ecological data

None

Molecular structure data

5. Molecular property data:


1. Molar refractive index: 56.33


2. Molar volume (m3/mol):177.7


3. Isotonic specific volume (90.2K ): 427.1


4. Surface Tension (dyne/cm):33.3


5. Polarizability10-24cm3):22.33

Compute chemical data

1. Reference value for hydrophobic parameter calculation (XlogP): 3.1

2. Number of hydrogen bond donors: 0

3. Number of hydrogen bond acceptors: 0

4. Number of rotatable chemical bonds: 1

5. Number of tautomers: none

6. Topological molecule polar surface area 4.9

7. Number of heavy atoms: 13

8. Surface charge: 0

9. Complexity: 151

10. Number of isotope atoms: 0

11. Determine the number of atomic stereocenters: 0

12. Uncertain number of atomic stereocenters: 0

13. Determine the number of chemical bond stereocenters: 0

14. Number of uncertain chemical bond stereocenters: 0

15. Number of covalent bond units: 1

Properties and stability

None

Storage method

None

Synthesis method

None

Purpose

None

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Methyl magnesium bromide

Methyl magnesium bromide structural formula

Structural formula

Business number 01J3
Molecular formula CH3MgBr
Molecular weight 119.24
label

Grignard reagent,

format reagent

Numbering system

CAS number:75-16-1

MDL number:MFCD00000041

EINECS number:200-844-1

RTECS number:OM3700000

BRN number:3535220

PubChem number:24858252

Physical property data

1. Properties: Solid

2. Density (g/mL, 20℃): 1.035

3. Relative vapor density (g/mL, air=1): Undetermined

4. Melting point (ºC): Undetermined

5. Boiling point (ºC, normal pressure): Undetermined

6. Boiling point (ºC, 5.2kPa): Not determined

7. Refractive index: Not determined

8. Flash point (ºF): 77

9. Specific rotation (º ): Undetermined

10. Autoignition point or ignition temperature (ºC): 160

11. Vapor pressure (kPa, 25ºC): Undetermined

12. Saturated vapor pressure (kPa, 60ºC) not determined:

13. Heat of combustion (KJ/mol): not determined

14. Critical temperature (ºC): not determined

15. Critical pressure (KPa): Undetermined

16. Log value of oil-water (octanol/water) partition coefficient: Undetermined

17. Explosion Upper limit (%, V/V): Undetermined

18. Lower explosion limit (%, V/V): Undetermined

19. Solubility: Reacts strongly with water, producing Combustible gas

Toxicological data

None

Ecological data

None

Molecular structure data

None

Compute chemical data

1. Reference value for hydrophobic parameter calculation (XlogP): None

2. Number of hydrogen bond donors: 0

3. Number of hydrogen bond acceptors: 2

4. Number of rotatable chemical bonds: 0

5. Number of tautomers: none

6. Topological molecule polar surface area 0

7. Number of heavy atoms: 3

8. Surface charge: 0

9. Complexity: 4.8

10. Number of isotope atoms: 0

11. Determine the number of atomic stereocenters: 0

12. Uncertain number of atomic stereocenters: 0

13. Determine the number of chemical bond stereocenters: 0

14. Number of uncertain chemical bond stereocenters: 0

15. Number of covalent bond units: 3

Properties and stability

Reacts with water, oxides, acids, alkalis, and alcohols.

Sensitive to water, light and air.

Storage method

Store in a cool, dry, well-ventilated non-combustible warehouse. Keep away from fire and heat sources. The warehouse temperature should not exceed 28℃.The packaging must be sealed and must not come into contact with air. Keep away from light. Not suitable for large quantities or long-term storage. It should be stored separately from acids, flammables, combustibles, oxidants, oxygen, compressed air, etc. The lighting, ventilation and other facilities in the storage room should be explosion-proof, and the switches should be located outside the warehouse. Equipped with the appropriate variety and quantity of fire equipment. Fire and explosion prevention technical measures must be taken during tank storage. It is prohibited to use mechanical equipment and tools that are prone to sparks. When handling, load and unload with care to prevent damage to packaging and containers. Smoking, drinking, and eating are not allowed at the operation site.

Synthesis method

Use carbide tools to cut single crystal magnesium flakes with a purity of 99.999%, wash them several times with ether treated with lithium aluminum tetrahydride, and add a dry ice-acetone condenser tube. And in the reaction bottle directly connected to the ether distillation device. The device is repeatedly baked with gas lamps and filled with high-purity nitrogen several times. Add dry ice to the condenser tube, evaporate 50 mL of ether directly into the flask, and then introduce a small amount of ethyl bromide from the side tube installed near the bottom of the condenser tube. Bubbles are released and heat is released, proving that the reaction has begun. Thereafter, continue to pass in methyl bromide and steam into ether. Keep methyl bromide and ether at reflux without heating until the magnesium metal reacts completely. During this period, it is appropriate to keep the ether solution at about 300 mL. Remove the flask in the nitrogen flow and put it in the operating box with a stopper, filter it into the flask with a glass sand funnel, and cover it with a tetrafluoroethylene piston. A colorless and transparent methylmagnesium bromide solution was obtained. The ratio of the analytical values ​​of C:Mg:Br is 1.00:1.03:0.99.


Purpose

for organic synthesis

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5-nitrosalicylicaldehyde

5-Nitrosalicylicaldehyde structural formula

Structural formula

Business number 02C8
Molecular formula C7H5NO4
Molecular weight 167.12
label

2-hydroxy-5-nitrobenzoyl,

2-Hydroxy5-nitrobenzaldehyae

Numbering system

CAS number:97-51-8

MDL number:MFCD00007337

EINECS number:202-587-0

RTECS number:CU6675000

BRN number:512565

PubChem number:24856642

Physical property data

  1. Appearance: light yellow or white powder.
  2. Density (g/mL, 20℃): Undetermined
  3. Relative vapor density (g/mL, air=1): Undetermined
  4. Melting point ( ºC): 125-128
  5. Boiling point (ºC, normal pressure): Undetermined
  6. Boiling point (ºC, KPa): Undetermined
  7. Refractive index: Undetermined Determined
  8. Flash point (ºC): Not determined
  9. Specific optical rotation (º): Not determined
  10. Autoignition point or ignition temperature (ºC): Not determined Determined
  11. Vapor pressure (mmHg, 20.2ºC): Undetermined
  12. Saturation vapor pressure (kPa, ºC): Undetermined
  13. Heat of combustion (KJ/mol ): Undetermined
  14. Critical temperature (ºC): Undetermined
  15. Critical pressure (KPa): Undetermined
  16. Oil-water (octanol/water) partition coefficient Log value: Undetermined
  17. Upper explosion limit (%, V/V): Undetermined
  18. Lower explosion limit (%, V/V): Undetermined
  19. Solubility: Not determined

Toxicological data

Acute toxicity: Rat oral LD50: 799mg/kg; Mouse oral LD50: 672mg/kg;

Ecological data

None

Molecular structure data

1. Molar refractive index: 41.43

2. Molar volume (cm3/mol): 111.3

3. Isotonic specific volume (90.2K ): 322.8

4. Surface tension (dyne/cm): 70.5

5. Polarizability (10-24cm3): 16.42

Compute chemical data

1. Reference value for hydrophobic parameter calculation (XlogP): None

2. Number of hydrogen bond donors: 1

3. Number of hydrogen bond acceptors: 4

4. Number of rotatable chemical bonds: 1

5. Number of tautomers: 4

6. Topological molecule polar surface area 83.1

7. Number of heavy atoms: 12

8. Surface charge: 0

9. Complexity: 188

10. Number of isotope atoms: 0

11. Determine the number of atomic stereocenters: 0

12. Uncertain number of atomic stereocenters: 0

13. Determine the number of chemical bond stereocenters: 0

14. Number of uncertain chemical bond stereocenters: 0

15. Number of covalent bond units: 1

Properties and stability

None

Storage method

None

Synthesis method

None

Purpose

Intermediates for organic synthesis of medicines, spices and dyes.

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carbon disulfide

Carbon disulfide structural formula

Structural formula

Business number 01J2
Molecular formula CS2
Molecular weight 76.14
label

carbon disulfide,

Dithoicarbonic anhydride,

Carbon bisulfide,

Aliphatic sulfur compounds

Numbering system

CAS number:75-15-0

MDL number:MFCD00011321

EINECS number:200-843-6

RTECS number:FF6650000

BRN number:1098293

PubChem number:24860298

Physical property data

1. Properties: colorless or light yellow transparent liquid with pungent odor and easy to evaporate. [1]

2. Melting point (℃): -111.5[2]

3. Boiling point (℃): 46.3[3]

4. Relative density (water = 1): 1.26[4]

5. Relative vapor Density (air=1): 2.63[5]

6. Saturated vapor pressure (kPa): 40 (20℃)[6]

7. Heat of combustion (kJ/mol): -1029.4[7]

8. Critical temperature (℃): 280[8]

9. Critical pressure (MPa): 7.39[9]

10. Octanol/water partition coefficient: 1.94 [10]

11. Flash point (℃): -30 (CC) [11]

12. Ignition temperature ( ℃): 90[12]

13. Explosion upper limit (%): 50.0[13]

14. Explosion Lower limit (%): 1.3[14]

15. Solubility: Insoluble in water, soluble in most organic solvents such as ethanol and ether. [15]

16. Refractive index (25ºC): 1.6241

17. Viscosity (mPa·s, 20ºC): 0.363

18. Ignition point (ºC): 100

19. Heat of evaporation (KJ/mol, 25ºC): 27.54

20. Heat of fusion (KJ/mol): 4.392

p>

21. Heat of formation (KJ/mol): 89.47

22. Specific heat capacity (KJ/(kg·K), 25ºC, constant pressure): 1.00

23 .Conductivity (S/m, 25ºC): 3.7×10-3

Toxicological data

1. Acute toxicity[16] LD50: 3188mg/kg (rat oral)

2. Irritation No data yet

3. Subacute and chronic toxicity[17] Rabbit inhalation 1.28g/m3, 5 months, causing chronic poisoning; 0.5~0.6g/m3, 6.5 months, causing an increase in serum cholesterol.

4. Mutagenicity [18] Microbial mutagenicity: Salmonella typhimurium 100μg/dish. Sister chromatid exchange: human lymphocytes 10200μg/L

5. Teratogenicity [19] Inhalation is the lowest in rats 1 to 22 days after pregnancy Toxic dose (TCLo) 10mg/m3 (8h) can cause eye and ear development malformations. Rats inhaled the lowest toxic dose (TCLo) 100 mg/m3 (8 hours) from 1 to 21 days after pregnancy, causing developmental malformations of the craniofacial region (including nose and tongue).

6. Others[20] Minimum toxic concentration for male inhalation (TCLo): 40mg/m3 (91 weeks ), causing changes in sperm production. The lowest toxic concentration for inhalation in rats (TCLo): 100mg/m3 (8h) (administered from 1st to 21st day of pregnancy), �� Started with fetal death and abnormal craniofacial development.

Ecological data

1. Ecotoxicity[21] LC50: 162~135mg/L (24~96h) (mosquito fish)

2. Biodegradability No data yet

3. Non-biodegradability[22] In the air, when hydroxyl radicals When the concentration is 5.00×105 pieces/cm3, the degradation half-life is 5.5d (theoretical).

4. Bioaccumulation [23] BCF: <6.1 (carp, contact concentration 50μg/L) <60 (carp, contact concentration 5μg/L)

Molecular structure data

1. Molar refractive index: 21.50

2. Molar volume (cm3/mol): 60.4

3. Isotonic specific volume (90.2K ): 143.8

4. Surface tension (dyne/cm): 32.0

5. Polarizability (10-24cm3): 8.52

Compute chemical data

1. Reference value for hydrophobic parameter calculation (XlogP): 2.1

2. Number of hydrogen bond donors: 0

3. Number of hydrogen bond acceptors: 2

4. Number of rotatable chemical bonds: 0

5. Number of tautomers: none

6. Topological molecule polar surface area 64.2

7. Number of heavy atoms: 3

8. Surface charge: 0

9. Complexity: 18.3

10. Number of isotope atoms: 0

11. Determine the number of atomic stereocenters: 0

12. Uncertain number of atomic stereocenters: 0

13. Determine the number of chemical bond stereocenters: 0

14. Number of uncertain chemical bond stereocenters: 0

15. Number of covalent bond units: 1

Properties and stability

1. Extremely flammable and can easily burn and explode when exposed to heat, sparks, flames or oxidants. Decomposes when heated to produce toxic sulfide fumes. Reacts violently with aluminum, zinc, potassium, fluorine, chlorine, azide, etc., posing a risk of combustion and explosion. High-speed impact and friction can cause combustion and explosion due to static spark discharge.

2. Chemical properties: Stable to acids, and does not interact with concentrated sulfuric acid and concentrated nitric acid at room temperature. But it is unstable to alkali and reacts with potassium hydroxide to generate potassium thiosulfate and potassium carbonate. It reacts with sodium alcohol to form xanthate; it gradually oxidizes in the air, becoming yellow and smelly. It decomposes under the influence of sunlight; at low temperatures, it reacts with water to form crystals with the structure of 2CS2·H2O. It reacts with chlorine under appropriate conditions to produce carbon tetrachloride and sulfur chloride.

3. The high-concentration vapor of this product has an anesthetic effect. The concentration is 0.1% to 0.3%. Inhalation can cause death in 1 hour. Even if it is lower than the lethal dose, it will leave sequelae. Long-term inhalation (3 months) 160 When ×10-6 or more, neuritis will occur after 1 to 2 years. The maximum allowable concentration in the workplace is 60mg/m3. This product is toxic and irritating. Closed operation, local exhaust. Operators must undergo special training and strictly abide by operating procedures. It is recommended that operators wear self-priming filter gas masks (half masks), chemical safety glasses, anti-static overalls, and rubber oil-resistant gloves. Keep away from fire and heat sources. Smoking is strictly prohibited in the workplace. Use explosion-proof ventilation systems and equipment. Prevent vapors from leaking into the workplace air. Avoid contact with oxidants, amines, and alkali metals. The flow rate should be controlled during filling, and a grounding device should be installed to prevent the accumulation of static electricity. Equipped with corresponding varieties and quantities of fire-fighting equipment and leakage emergency treatment equipment. Empty containers may be harmful residues.

4. Due to its low boiling point, strong volatility and high toxicity, it is easily dispersed in the air during production and use, causing serious pollution and harm to the environment and human body. Carbon disulfide is a poison that damages nerves and blood vessels. When people are exposed to high concentrations of carbon disulfide, it has a paralyzing effect. If it lasts for a long time, the respiratory center may be paralyzed, resulting in loss of consciousness and death. At high concentrations, it can also be absorbed by human skin.

5. This product is a gas anesthetic. Its vapor has a strong irritating effect on the skin and eyes, and can easily cause dermatitis and burns. Acute poisoning begins to cause delirium, and later anesthesia, loss of consciousness, and even death from respiratory failure. Long-term inhalation of its vapor can cause symptoms such as weak stomach, insomnia, fatigue, loss of appetite, headache, dizziness, abnormal sensation, drop in blood pressure, trembling, stiffness of hands and feet, slow movement, salivation, sweating, memory loss and other symptoms. Mainly damages the nervous and cardiovascular systems. When the vapor concentration is 12440 mg/m3, death will occur in 30 to 60 minutes. TJ 36-79 stipulates that the maximum allowable concentration in workshop air is 10 mg/m3.

6. Stability[24] Stable

7. Incompatible substances[25] Strong oxidizing agent, aluminum

8. Conditions to avoid contact[26] Heating

9. Polymerization hazard[27] No polymerization

10. Decomposition products[28] Hydrogen chloride

Storage method

1. Storage precautions[29] It is easily volatile at room temperature, so the surface of the container can be covered with water. Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature should not exceed 29°C. Keep container tightly sealed. They should be stored separately from oxidants, amines, alkali metals, and food chemicals, and avoid mixed storage. Use explosion-proof lighting and ventilation facilities. It is prohibited to use mechanical equipment and tools that are prone to sparks. The storage area should be equipped with leakage emergency treatment equipmentequipment and suitable containment materials.

2. This product is packed in glass bottles and metal barrels (aluminum barrels, iron barrels, storage tanks) and protected by wooden boxes, and must be stored in In a warehouse constructed of non-combustible materials and with ground ventilation facilities, keep away from fire sources and avoid sunlight. In summer, cooling measures should be taken to keep storage below 17°C. There should be no electrical equipment or heating facilities near the warehouse, and lightning or static electricity must be prevented from igniting fires. The liquid level of the storage tank should be sealed with inert gas. Store and transport according to regulations for flammable materials.

Synthesis method

1. Methane sulfur method: solid sulfur is heated and melted into liquid, and then purified with activated clay. Natural gas purification treatment uses light diesel to adsorb fractions above C2 and separate pure methane gas. After the natural gas and sulfur vapor are heated, they can be fully mixed and heated to 650°C, and then sent to the reactor for reaction. The pressurized partial condensation method is used to separate carbon disulfide and hydrogen sulfide, and carbon disulfide is obtained after distillation. The reaction formula is as follows:

2. Charcoal sulfur method : According to different heating methods, it can be divided into two categories: external heating iron steamer method and internal heating electric furnace method. Generally, the three-phase electric furnace method is used. In the electric furnace method, charcoal is directly roasted at 800°C to remove moisture and organic matter and then added to the electric furnace intermittently. Molten sulfur is continuously added to the electric furnace to react with the red charcoal at about 1000°C. The generated carbon disulfide is desulfurized and condensed to obtain a crude product, which is then refined. Distillation and condensation to obtain carbon disulfide finished product. The reaction formula is as follows:

3. Commercially available Carbon disulfide is synthesized by heating charcoal and sulfur to 850 to 950°C. As a reagent, it can meet general requirements, but when the required purity is high, the following methods need to be used to remove the impurities contained in it. These impurities are hydrogen sulfide, sulfurous acid, sulfuric acid, organic sulfides, water and sulfur. Add 100 to 200 g of mercury and an appropriate amount of phosphorus pentoxide to 500 mL of commercially available carbon disulfide, shake for about 1 hour, filter, fractionate the filtrate away from light, discard the high and low fractions, and collect the middle fraction. The collected fractions are remixed with mercury and phosphorus pentoxide, shaken, and fractionated. Repeat this operation until the content of harmful impurities reaches the standard.

Refining method: Impurities contained include sulfur, sulfide and water. There are several refining methods: ① Distill 3 times with a glass still. ② Dry with calcium chloride and then fractionate multiple times. ③ Shake with mercury to remove sulfide, then dry and fractionate with phosphorus pentoxide. ④ Add 5g of crushed potassium permanganate to 1L of carbon disulfide and shake it thoroughly until the hydrogen sulfide is completely removed and then place it. After separation, add a small amount of mercury and shake it to remove the sulfur until the interface does not turn black further. Finally, add 5g of mercury sulfate to each 1L of carbon disulfide and shake to eliminate the odor. After separation, it is dried with calcium chloride and fractionated.

4. Use industrial carbon disulfide as raw material, add anhydrous copper sulfate (25-37.5g copper sulfate is required for each carbon disulfide), stir thoroughly until the black powder disappears and there is no unpleasant smell, immediately Filter to remove insoluble impurities, then add anhydrous copper sulfate to the filtrate, distill, and collect the fractions according to product specifications, which is the pure product.

Purpose

1. Used in the manufacture of viscose fiber, cellophane, xanthate, thiocyanate and carbon tetrachloride. Xanthate produced from carbon disulfide is used as an ore flotation agent in the metallurgical industry. Used in the production of agricultural pesticides. When vulcanized in the rubber industry, it can be used as a solvent for sulfur chloride. Use it to make anti-corrosion agents for equipment and pipelines in ammonia treatment systems. It is also a solvent used for testing primary amines, secondary amines and α-amino acids, measuring refractive index, and chromatographic analysis. It is also used to extract oil from linseed, olive fruit, animal bones, leather and wool. Used as an accelerator in aviation. It is also used as a solvent for grease, wax, paint, camphor, resin, rubber, sulfur, phosphorus, iodine, etc., as a degreaser for wool, as an agricultural pesticide, as a soil disinfectant, as a stain remover for clothes, etc. In analysis, it is used for the determination of primary amines, secondary amines and α-amino acids and as a solvent for infrared spectroscopy.

2. Carbon disulfide is widely used in metallurgy, pesticides, rubber, viscose fiber and other industrial fields. It has good penetrability and is generally used as a mixture with non-combustible ingredients when fumigating grain. Fumigation of dry seeds with carbon disulfide does not reduce seed viability. For grains such as wheat, barley, corn, rice, etc., fumigation at 250g/m3 for 24 hours will not affect germination. Gaseous carbon disulfide will seriously damage or kill growing plants or seedlings. Water-diluted carbon disulfide emulsion treats the soil around the roots of evergreen trees and deciduous seedlings, and can effectively control a variety of underground pests. Due to the flammable and explosive properties of carbon disulfide, this agent is used less and less in modern fumigations.

3. Mainly used as raw material for manufacturing viscose fiber and cellophane. Xanthate produced from carbon disulfide is used as an ore flotation agent in the metallurgical industry. Used in the production of agricultural pesticides. When vulcanized in the rubber industry, it can be used as a solvent for sulfur chloride. It is also a solvent used for testing primary amines, secondary amines and α-amino acids, measuring refractive index, and chromatographic analysis. It is also used to extract oil from linseed, olive fruit, animal bones, leather and wool. Used as aerospace accelerator.

4. Used as analytical reagents, solvents, viscose fibersVJ wool degreaser. Also used for refractive index determination.

5. Used in the manufacture of rayon, pesticides, accelerator M, accelerator D, and also used as solvents. [30]

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5-Chloro-2,4-dimethoxyaniline

5-chloro-2,4-dimethoxyaniline structural formula

Structural formula

Business number 02C7
Molecular formula C8H10ClNO2
Molecular weight 187.62
label

2,4-Dimethoxy-5-chloroaniline

Numbering system

CAS number:97-50-7

MDL number:MFCD00025752

EINECS number:202-586-5

RTECS number:None

BRN number:2211013

PubChem number:24862121

Physical property data

  1. Characteristics: white to light gray crystal.
  2. Density (g/mL, 20℃): Undetermined
  3. Relative vapor density (g/mL, air=1): Undetermined
  4. Melting point ( ºC): 89-92
  5. Boiling point (ºC, normal pressure): Undetermined
  6. Boiling point (ºC, KPa): Undetermined
  7. Refractive index: Undetermined Determined
  8. Flash point (ºC): Not determined
  9. Specific optical rotation (º): Not determined
  10. Autoignition point or ignition temperature (ºC): Not determined Determined
  11. Vapor pressure (mmHg, 20.2ºC): Undetermined
  12. Saturation vapor pressure (kPa, ºC): Undetermined
  13. Heat of combustion (KJ/mol ): Undetermined
  14. Critical temperature (ºC): Undetermined
  15. Critical pressure (KPa): Undetermined
  16. Oil-water (octanol/water) partition coefficient Log value: Undetermined
  17. Upper explosion limit (%, V/V): Undetermined
  18. Lower explosion limit (%, V/V): Undetermined
  19. Solubility: Not determined

Toxicological data

None

Ecological data

None

Molecular structure data

1. Molar refractive index: 45.64

2. Molar volume (cm3/mol): 132.6

3. Isotonic specific volume (90.2K ): 359.2

4. Surface tension (dyne/cm): 53.7

5. Polarizability (10-24cm3): 18.09

Compute chemical data

1. Reference value for hydrophobic parameter calculation (XlogP): 1.8

2. Number of hydrogen bond donors: 1

3. Number of hydrogen bond acceptors: 3

4. Number of rotatable chemical bonds: 2

5. Number of tautomers: none

6. Topological molecule polar surface area 44.5

7. Number of heavy atoms: 12

8. Surface charge: 0

9. Complexity: 145

10. Number of isotope atoms: 0

11. Determine the number of atomic stereocenters: 0

12. Uncertain number of atomic stereocenters: 0

13. Determine the number of chemical bond stereocenters: 0

14. Number of uncertain chemical bond stereocenters: 0

15. Number of covalent bond units: 1

Properties and stability

None

Storage method

None

Synthesis method

None

Purpose

Used in the synthesis of naphthol AS-ITR, Pigment Red 5 and other dyes and their intermediates.

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DL-glyceraldehyde

DL-glyceraldehyde structural formula

Structural formula

Business number 017X
Molecular formula C3H6O3
Molecular weight 90.08
label

None

Numbering system

CAS number:56-82-6

MDL number:MFCD00064379

EINECS number:200-290-0

RTECS number:MA6475000

BRN number:635685

PubChem number:24895192

Physical property data

1. Properties: white crystal.

2. Density (g/mL, 25/4℃): 1.445

3. Relative vapor density (g/mL, air=1): Undetermined

4. Melting point (ºC): 145

5. Boiling point (ºC, normal pressure): Undetermined

6. Boiling point (ºC, 5.2kPa): Undetermined

7. Refractive index: Undetermined

8. Flash point (ºC): Undetermined

9. Specific rotation (º): Undetermined

7. p>

10. Autoignition point or ignition temperature (ºC): Undetermined

11. Vapor pressure (kPa, 25ºC): Undetermined

12. Saturated vapor pressure (kPa, 60ºC): Undetermined

13. Heat of combustion (KJ/mol): Undetermined

14. Critical temperature (ºC): Undetermined

15. Critical pressure (KPa): Undetermined

16. Log value of oil-water (octanol/water) partition coefficient: Undetermined

17. Explosion upper limit (%, V /V): Undetermined

18. Lower explosion limit (%, V/V): Undetermined

19. Solubility: Slightly soluble in water, insoluble in benzene and petroleum ether and pentane.

Toxicological data

1. Acute toxicity: rat abdominal LD50: 2mg/kg 2. Mutagenicity: mutation microorganismsTEST system: bacteria – Salmonella typhimurium: 100ug/plate

Ecological data

None

Molecular structure data

5. Molecular property data:

1. Molar refractive index: 19.16

2. Molar volume (cm3/mol): 70.7

3. Isotonic specific volume (90.2K): 191.2

4. Surface tension (dyne/cm): 53.3

5. Polarizability (10-24cm3): 7.59

Compute chemical data

1. Reference value for calculation of hydrophobic parameters (XlogP): -1.6

2. Number of hydrogen bond donors: 2

3. Number of hydrogen bond acceptors: 3

p>

4. Number of rotatable chemical bonds: 2

5. Number of tautomers: 3

6. Topological molecule polar surface area 57.5

7. Number of heavy atoms: 6

8. Surface charge: 0

9. Complexity: 43.3

10. Number of isotope atoms: 0

11. Determine the number of atomic stereocenters: 0

12. Uncertain number of atomic stereocenters: 1

13. Determine ��Number of stereocenters of chemical bonds: 0

14. Number of stereocenters of uncertain chemical bonds: 0

15. Number of covalent bond units: 1

Properties and stability

None

Storage method

This product should be stored in a sealed, cool place and away from light.

Synthesis method

1. Mix 50g (0.3mol) diethanol acetal DL-glyceraldehyde and 500ml 0.1mol/L sulfuric acid, and place at 20°C for 7 days. After adding 30ml of glacial acetic acid, neutralize with barium hydroxide solution, add 5g of activated carbon, stir and filter. The water in the filtrate was evaporated under reduced pressure, and an equal volume of absolute ethanol was added to the residue. The crystals were filtered out and dried to obtain 22g DL-glyceraldehyde, with a yield of 80%.

2. Preparation method:

Dietol-β-chloroacetaldehyde (3): In a 3L reaction bottle equipped with a stirrer and ventilation tube, add 253 mL of absolute ethanol, cool it to below 0°C in an ice-salt bath, and dry it of hydrogen chloride gas to saturation. While stirring, 112g (2.0 mol) of acrolein (2) cooled to 0°C was added dropwise, the reaction temperature was controlled to 0°C, and the addition was completed in about 1.5 hours. Let stand and separate the layers, separate the lower organic layer, add solid sodium bicarbonate powder in batches, neutralize and remove acid. Filter, wash the filtrate with ice water, and dry over anhydrous potassium carbonate for 10 hours. After filtration, distill under reduced pressure and collect the fractions at 58-62°C/1.06kPa to obtain 112g of diethanol-β-chloroacetaldehyde (3) with a yield of 34%. Diethanol acrolein (4): Add 340g (6mol) of dry powdered potassium hydroxide and 167g (1.0mol) of the above compound (3) into a distillation bottle. After shaking vigorously, install a fractionation device. Heat the distillation bottle in an oil bath at 210 to 220°C until no more distillate is distilled. The water in the distillate was separated, and the organic layer was dried with potassium carbonate, filtered and distilled. The fractions at 122-126°C were collected to obtain 98g of diethanol acrolein (4), with a yield of 75%. Diethylglyceraldehyde (5): In a reaction bottle equipped with a stirrer, thermometer, and dropping funnel, add 65g (0.5mol) of diethylglyceraldehyde (4) and 600mL of water, cool to 5°C, and stir Add dropwise a solution of 80g (0.5mol) water, control the dropping speed to about 25mL/min, and keep the temperature of the reaction solution at about 5°C. Stirring – stop, the reactants will become gel-like. After leaving it for 2 hours, heat it in a steam bath for 1 hour. Filter with suction, and wash the manganese dioxide with 150 mL of water. Combine the filtrate and washing liquid, and add 1200g anhydrous potassium carbonate while cooling. The organic layer was separated, and the aqueous layer was extracted 4 times with diethyl ether. The organic layers were combined and dried over anhydrous potassium carbonate. After recovering the diethyl ether, distill under reduced pressure and collect the fraction at 120-121°C/1.06kPa to obtain 55g of diethyl glyceraldehyde (5) with a yield of 67%. DL-Glyceraldehyde (1): Place 50g (0.3mol) of the above-mentioned diethanol glyceraldehyde (5) and 0.05mol/L sulfuric acid in a reaction bottle, and place it at 20°C for 1 week. Add 30 mL of glacial acetic acid. The reaction compound was carefully neutralized with barium hydroxide solution and decolorized with activated carbon. Filter, and the filtrate is concentrated at a pressure of 1.33kPa. Add an equal volume of absolute ethanol to the remainder and slowly crystallize. Filter the precipitated crystals and vacuum dry them in a vacuum dryer containing soda lime and calcium chloride desiccant to obtain 22g of DL-glyceraldehyde (1) with a yield of 80%. [1]

Purpose

Used in biochemical research, organic synthesis intermediates, and nutritional agents.

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formamide

Formamide structural formula

Structural formula

Business number 01J1
Molecular formula CH3NO
Molecular weight 45.04
label

Aminoformaldehyde,

Methanamide,

Carbamaldehyde,

Reagents for genetic engineering research,

paper treatment agent,

Softeners for the fiber industry,

Softener for animal glue,

Reaction solvents for organic synthesis

Numbering system

CAS number:75-12-7

MDL number:MFCD00007941

EINECS number:200-842-0

RTECS number:LQ0525000

BRN number:505995

PubChem number:24894985

Physical property data

1. Properties: Colorless and transparent viscous liquid with a slight ammonia smell and hygroscopicity.

2. Boiling point (ºC, 101.3kPa, partially decomposed): 220, 70.5ºC (133.3pa)

3. Melting point (ºC): 2.55~3

4. Relative density (g/mL, 20/4ºC): 1.13339

5. Relative density (g/mL, 25/4ºC): 1.134

6. Relative steam Density (g/mL, air=1): 1.55

7. Refractive index (20ºC): 1.447

8. Refractive index (25ºC): 1.44682

9. Viscosity (mPa·s, 20ºC): 3.764

10. Viscosity (mPa·s, 25ºC): 3.302

11. Flash point (ºC, closed): 175

12. Flash point (ºC, open): 150

13. Fire point (ºC): >500

14. Heat of vaporization (KJ/mol, 25ºC): 65.021

15. Heat of fusion (KJ/mol): 6.699

16. Heat of formation (KJ/mol, 25ºC, liquid): -254.1

17. Heat of combustion (KJ/mol, 25ºC, liquid): 568.6

18. Specific heat capacity (KJ/(kg·K), 25ºC, constant pressure): 2.39

19. Conductivity (S/m): <2×10-1

20. Solubility: Can be dissolved with water, alcohol, ethylene glycol, acetone, acetic acid, dihydrogen Miscible with alkane, glycerin, phenol, etc. But it is almost insoluble in aliphatic hydrocarbons, aromatic hydrocarbons, ethers, chlorinated hydrocarbons, chlorobenzene, nitrobenzene, etc.

Toxicological data

Formamide has an irritating effect on the skin and mucous membranes, can occasionally cause allergies, and can be absorbed by the skin. The oral lethal dose LD for rats is 7500 mg/kg. Rat oral LD50>4000mg/kg. Dermal toxicity in guinea pigs is LD50<5mL/kg and LD50 is 2539mg/kg.

Ecological data

None

Molecular structure data

1. Molar refractive index: 10.40

2. Molar volume (cm3/mol): 46.0

3. Isotonic specific volume (90.2K): 109.8

4. Surface tension (dyne/cm): 32.4

5. Polarizability (10-24cm3): 4.12 p>

Compute chemical data

1. Hydrophobic parameter calculation reference value (XlogP): -0.8

2. Number of hydrogen bond donors: 1

3. Number of hydrogen bond acceptors: 1

p>

4. Number of rotatable chemical bonds: 0

5. Number of tautomers: 2

6. Topological molecular polar surface area (TPSA): 43.1

7. Number of heavy atoms: 3

8. Surface charge: 0

9. Complexity: 12.3

10. Isotopic atoms Quantity: 0

11. Determine the number of atomic stereocenters: 0

12. Uncertain number of atomic stereocenters: 0

13. Determine the chemical bond structure Number of stereocenters: 0

14, Number of uncertain chemical bond stereocenters: 0

15, Number of covalent bond units: 1

Properties and stability

1. Chemical properties: The alkalinity of formamide is very weak, so the salt formed with strong acid is very unstable. Formamide is easily hydrolyzed to ammonium formate in aqueous solution. Ammonium formate is heated and dehydrated to form formamide again:

The hydrolysis rate of formamide is very slow at room temperature, but it is actually relatively stable. However, the hydrolysis rate is relatively fast at high temperatures, especially in the presence of acids and alkalis. There are two ways to pyrolyze formamide: it decomposes into ammonia and carbon monoxide when boiled under normal pressure:

When gaseous formamide is pyrolyzed at 400~600°C in the presence of a dehydrating agent, hydrogen cyanide is obtained , yield 90%:

The adduct formed by formamide and strong acid is very reactive and can undergo the following reactions:

Formamide reacts with alcohol in the presence of hydrogen chloride to form formate. . It reacts with hypochlorous acid in a cold water bath to form N,N-dichloroformamide HCONCl2. This compound is explosive when pure. It reacts with metal potassium and sodium to form a metal compound such as diformamide (HCO)2NH. Photochemical reactions with alkenes produce fatty acid amides. Reacts with alkyl halides at 150°C to form formamide compounds and formic esters:

Formamide reacts with metal salts to form substitutions or adducts:

Formamide reacts with pentoxide Dehydration under the action of diphosphorus produces hydrogen cyanide.

2.This product has low toxicity. Temporarily irritating to skin and mucous membranes. The oral LC50 of mice is greater than 1000mg/kg. Wear protective equipment for long-term exposure.

3. Exist in smoke.
 

Storage method

1. This product should be kept sealed, cool and dry. Keep sealed, avoid contact with water, and store in a cool and ventilated place.

2. Formamide products can be stored and transported in stainless steel or aluminum tanks (tank trucks) or tank-type containers as well as 60kg and 220kg drums. The container material can be polyethylene or polyethylene-lined steel. Keep sealed, avoid contact with water, and store in a cool and ventilated place.

Synthesis method

1. Two-step method: The first step is to generate methyl formate from carbon monoxide and methanol under the action of sodium methoxide. In the second step, methyl formate is ammonolyzed to form formamide, and the reaction conditions are 80-100°C and 0.2-0.6MPa. This method has fewer problems.

2. Formic acid method Formic acid and methanol First, esterification reaction is performed to generate methyl formate, and then ammonolysis is performed to generate formamide, and then distillation is performed to separate methanol and impurities to obtain the finished product. This method has become obsolete due to its high cost.

3. One-step method consists of carbon monoxide and Ammonia is catalyzed by sodium methoxide to directly synthesize formamide through high pressure (10-30MPa) and temperature of 80-100℃

4. Formic acid and urea method.

5. The new method consists of sodium formate and Ammonium salt reacts under certain temperature and pressure to form formamide. This method is a domestic patent invention.

Refining method: Formamide is produced on a large scale from carbon monoxide and ammonia at 15~20MPa and 200℃. It can also be obtained by heating ammonium formate or the reaction between formate and ammonia. Therefore, it often contains water, ammonia, methanol, formate and ammonium formate. The purity of formamide can be improved by using fractional distillation under reduced pressure or fractional crystallization. Formamide used for determination of physical constants can be refined by adding a few drops of bromothymol blue to formamide. Neutralize with sodium hydroxide, heat the neutralized solution at 80 to 90°C under reduced pressure, and then neutralize. Repeat the operation several times until the solution remains neutral during heating. Then add sodium formate and distill under reduced pressure at 80~90°C. The distillate is neutralized and then distilled, and the next 4/5 fractions are collected to obtain formamide with a melting point of 2.2°C.

6.Ammonium formate is heated and decomposed to obtain formamide, which is then refined through distillation:

Purpose

1. Formamide has active reactivity and special solubility. It can be used as a raw material for organic synthesis, paper treatment agent, softener in the fiber industry, softener for animal glue, and also used to determine the amino acid content in rice. Analytical reagents. In organic synthesis, it is mostly used in medicine, and it also has many uses in pesticides, dyes, pigments, spices, and auxiliaries. It is also an excellent organic solvent and is mainly used in the spinning of acrylonitrile copolymers and ion exchange resins, as well as in the anti-static coating or conductive coating of plastic products. In addition, it is also used to separate chlorosilanes, purify oils, etc. Formamide can undergo a variety of reactions. In addition to the participation of three hydrogens in the reaction, it can also undergo dehydration, removal of CO, introduction of amino groups, introduction of acyl groups and cyclization reactions. Take Ringhe as an example. Diethyl malonate is cyclized with formamide to obtain the intermediate 4,6-dihydroxypyrimidine of vitamin B4. Anthranilic acid is cyclized with an amide to obtain the antiarrhythmic croroline intermediate quinazolone-4. 3-Amino-4-ethoxycarbonylpyrazole is cyclized with carboxamide to obtain the xanthine oxidase inhibitor allopurinol . The anticancer drug ethyleneimine is obtained by cyclizing ethylenediaminetetraacetic acid with formamide. Methyl ethyl methoxymalonate is cyclized with formamide to obtain disodium 5-methoxy-4,6-dihydroxypyrimidine, an intermediate of sulfonamide drugs.

2. Since formamide can dissolve inorganic salts and proteins with high dielectric constants, it can be used in the electrolysis and electroplating industries, as well as as reaction solvents and refining solvents for organic synthesis. In addition, formamide is also used as a raw material for medicines, dyes, spices, etc., as a treatment agent for paper, as a softener in the fiber industry, and as a softener for animal glue.

3.Used as raw material for organic synthesis. Polar solvent for organic reactions. Liquid chromatography solvents and eluents.

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acetylsamine

Acetylarsine Structural Formula

Structural formula

Business number 02C6
Molecular formula C8H10AsNO5
Molecular weight 275.09
label

acetapine,

3-acetamido-4-hydroxyphenylarsonic acid,

acetylsamine,

Acetaminophen Hydroxybenzoic Acid,

Acetamide arsine,

N-Acetyl-4-hydroxy-m-arsanilic acid,

[3-(Acetylamino)-4-hydroxyphenyl)]arsonic acid,

Acetphenarsine

Numbering system

CAS number:97-44-9

MDL number:MFCD00019936

EINECS number:202-582-3

RTECS number:CF8400000

BRN number:None

PubChem number:24890414

Physical property data

1. Properties: White prismatic crystals, odorless.

2. Density (g/mL, 20℃): Undetermined

3. Relative vapor density (g/mL, air=1): Undetermined

4. Melting point (ºC): 240-250℃ (decomposition)

5. Boiling point (ºC, normal pressure): Undetermined

6. Boiling point (ºC, KPa) : Undetermined

7. Refractive index: Undetermined

8. Flash point (ºC): Undetermined

9. Specific rotation (º): Not determined

10. Autoignition point or ignition temperature (ºC): Not determined

11. Vapor pressure (mmHg, 20.2ºC): Not determined

12. Saturated vapor pressure (kPa, ºC): Undetermined

13. Heat of combustion (KJ/mol): Undetermined

14. Critical temperature (ºC): Undetermined

15. Critical pressure (KPa): Undetermined

16. Log value of oil-water (octanol/water) partition coefficient: Undetermined

17. Explosion Upper limit (%, V/V): Undetermined

18. Lower explosion limit (%, V/V): Undetermined

19. Solubility: Slightly soluble in cold water and ethanol and dilute acids, soluble in boiling water, caustic alkali solutions or carbonic acid alkali solutions.

Toxicological data

Rat oral LD50 is 4mg/kg

Ecological data

None

Molecular structure data

None

Compute chemical data

1. Reference value for hydrophobic parameter calculation (XlogP): None

2. Number of hydrogen bond donors: 4

3. Number of hydrogen bond acceptors: 5

4. Number of rotatable chemical bonds: 2

5. Number of tautomers: 10

6. Topological molecule polar surface area 107

7. Number of heavy atoms: 15

8. Surface charge: 0

9. Complexity: 289

10. Number of isotope atoms: 0

11. Determine the number of atomic stereocenters: 0

12. Uncertain.Number of ��stereocenters: 0

13. Determine the number of stereocenters of chemical bonds: 0

14. Uncertain number of stereocenters of chemical bonds: 0

15. Number of covalent bond units: 1

Properties and stability

1. Highly toxic.

Storage method

Stored sealed and protected from light.

Synthesis method

Originated from acetylation of 1.3-amino-4-hydroxyphenylarsonic acid. Add 3-amino-4-hydroxyphenylarsonic acid to 5% sodium hydroxide solution and stir until completely dissolved. Adjust pH to 8, heat to 30-35°C, add acetic anhydride under vigorous stirring to precipitate, continue stirring for 1 hour, add hydrochloric acid at 55-60°C to precipitate crystals, filter, and wash with water to obtain crude acetylsamine. Refining: Dissolve the crude product in 5% sodium hydroxide solution, add activated carbon, stir, filter, and slowly add 10% sulfuric acid to the filtrate to make the Congo red test paper turn blue and precipitate crystals. Filter and wash to obtain refined acetylsamine.

Purpose

1. Medicine. Disinfectant, has the effect of killing trichomoniasis, and is used to treat vaginal trichomoniasis. It is often made into Diweijing tablets, each tablet contains 0.25g of acetylsamine and 0.30g of boric acid.

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Diiodomethane

Diiodomethane structural formula

Structural formula

Business number 01J0
Molecular formula CH2I2
Molecular weight 267.84
label

methylene iodide,

methine iodide,

methylene diiodide,

methylene iodide,

Methylene iodide,

Methylene diodide,

Aliphatic halogenated derivatives

Numbering system

CAS number:75-11-6

MDL number:MFCD00001079

EINECS number:200-841-5

RTECS number:PA8575000

BRN number:1696892

PubChem number:24849735

Physical property data

1. Properties: colorless clear to light yellow liquid. [14]

2. Melting point (℃): 5~6[15]

3. Boiling point (℃) : 181 (decomposition) [16]

4. Relative density (water = 1): 3.32[17]

5. Relative vapor density (air = 1): 9.25[18]

6. Heat of combustion (kJ/mol): -745.7[19]

7. Critical pressure (MPa): 5.47[20]

8. Octanol/water partition coefficient: 2.3[21]

9. Flash point (℃): 110[22]

10. Solubility: insoluble in water, soluble in ethanol, Most organic solvents such as ether, benzene, and chloroform. [23]

11. Refractive index at room temperature (n20): 1.7411

12. Refractive index at room temperature (n25): 1.7380

13. Solubility parameter (J·cm-3)0.5: 24.055

14.van der Waals area (cm2·mol-1): 6.430×109

15. van der Waals volume (cm3·mol-1): 50.930

16. Viscosity (10ºC): 3.35mPa. s

17. Liquid phase standard claimed heat (enthalpy) (kJ·mol-1): 67.8

18. Liquid phase standard hot melt (J ·mol-1·K-1): 135.5

19. The gas phase standard claims heat (enthalpy) (kJ·mol-1 ): 118.7

20. Gas phase standard entropy (J·mol-1·K-1): 309.50

21. Gas phase standard formation free energy (kJ·mol-1): 101.7

22. Gas phase standard hot melt (J·mol-1 sup>·K-1): 57.73

Toxicological data

1. Acute toxicity

Children’s oral LDLO: 2778 uL/kg

Rat abdominal LD50: 403mg/kg

Mouse abdominal LD50: 467mg /kg

Mouse subcutaneous LD50: 830mg/kg

2. Acute toxicity[24] LD50: 403mg/kg (rat oral); 830mg/kg (rat transdermal)

3. Irritation No data available

4. Mutagenicity [25] Microbial mutagenicity: Escherichia coli 3mg/dish.

Ecological data

1. Ecotoxicity No data available

2. Biodegradability No data available

3. Non-biodegradability No information yet

4. Other harmful effects This substance is harmful to the environment and attention should be paid to atmospheric pollution. [26]

Molecular structure data

1. Molar refractive index: 32.62

2. Molar volume (cm3/mol): 82.6

3. Isotonic specific volume (90.2K ): 219.9

4. Surface tension (dyne/cm): 50.0

5. Polarizability (10-24cm3): 12.93

Compute chemical data

1. Reference value for hydrophobic parameter calculation (XlogP): 2.3

2. Number of hydrogen bond donors: 0

3. Number of hydrogen bond acceptors: 0

4. Number of rotatable chemical bonds: 0

5. Number of tautomers:

6. Topological molecular polar surface area (TPSA): 0

7. Number of heavy atoms: 3

8. Surface charge: 0

9. Complexity: 2.8

10. Number of isotope atoms: 0

11. Determine the number of atomic stereocenters: 0

12. Uncertain number of atomic stereocenters: 0

13. Determine the number of chemical bond stereocenters Number: 0

14. Number of uncertain chemical bond stereocenters: 0

15. Number of covalent bond units: 1

Properties and stability

1. Toxic. Less anesthetic than methylene bromide.

2. Cause headache and difficulty breathing after smelling it. See Dibromomethane.

3. Storing it with copper powder can effectively prevent its decomposition; care should be taken to protect it from light; it cannot coexist with many metals (such as Al, Mg, Na, etc.) and strong alkali; there is certain corrosion safety; operate in a fume hood.

4. Stability[27] Stable

5. Incompatible substances[28] Strong oxidants, strong bases, alkali metals

6. Conditions to avoid contact[29] Heat and light

7. Polymerization hazard[30] No polymerization

8. Decomposition products[31] Iodide

Storage method

Storage Precautions[32] Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Keep container tightly sealed. They should be stored separately from oxidants, alkalis, alkali metals, and food chemicals, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. The storage area should be equipped with emergency release equipment and suitable containment materials.

Synthesis method

1. The iodoform and sodium arsenite method first uses arsenic trioxide and liquid alkali to react to prepare sodium arsenite, then mix the iodoform and sodium arsenite solutions, heat to 60~65°C with stirring, and then Add sodium hydroxide to produce diiodomethane in a one-step reaction. The reaction product is washed with water, distilled, decolorized, crystallized, separated and dried to obtain the finished product.

2. The effect of iodoform method and sodium acetate The reaction formula is as follows:

After the above reaction is completed, The finished product is obtained by distillation.

3. The phase transfer catalytic synthesis method uses triethylbenzyl ammonium chloride as the catalyst and is obtained by the reaction of dichloromethane and sodium iodide. The reaction formula is as follows:

Purpose

1. Organic synthetic raw materials, chemical reagents and pharmaceutical intermediates can be used to manufacture X-ray contrast agents, determine mineral density and refractive index, and separate minerals, etc.

2. Diiodomethane is a methylene transfer reagent that can react with different metals or alkyl metals to form carbenes, undergo cyclopropanation reactions with alkenes, and can also react with carbonyl groups to form methylene groups. chemical reaction. At the same time, nucleophiles such as ICH2M and I2CHM can also be prepared, and can also participate in free radical coupling reactions.

Methylene Many carbonyl methylation reagents use diiodomethane as the carbon source, which can be used as an alternative to the Wittig reaction; in the presence of ketones, diiodomethane The reaction of methane and magnesium amalgam can produce olefins (formula 1) in high yields[1]. This reaction can occur with aldehydes and ketones of different structures.

The presence of Lewis acid can greatly Accelerate the reaction and improve the selectivity and yield of the reaction. Commonly used Lewis acids include trimethylaluminum, titanium tetraisopropoxide, titanium tetrachloride, di(cyclopentadienyl)zirconium dichloride, etc. Among them, CH2I2/Zn/ Me3Al and CH2Br2/Zn/TiCl4The two groups of reagents have the best effect. In the presence of ketones, aldehydes can selectively undergo methylation reactions (Formula 2)[2].

Cyclopropanation In organic synthesis, diiodomethane is mainly used to carry out cyclopropanation reactions involving metals. The most important is zinc-involved cyclopropanation (Simmons-Smith reaction), a reagent that is widely used and capable of many variations. ZincThe source is crucial to the success or failure of the reaction. Zn/Cu, diethyl zinc, etc. can be used as sources of Zn for cyclopropanation reaction. Diiodomethane and samarium mercury or samarium iodide can be combined to obtain many different samarium-containing olefin cyclopropanation reagents, all of which can react with allyl alcohol and enol. α,β-unsaturated esters and α,β-unsaturated amides can also be combined with samarium catalysis Diiodomethane undergoes cyclopropanation reaction (Formula 3)[3]. The cyclopropanation reactions of zinc-containing reagents and samarium-containing reagents are directly affected by hydroxyl groups [4]. Treating diiodomethane with trialkyl aluminum (such as triisobutylaluminum) will also give the corresponding cyclopropane, which is a good complement to the zinc and samarium system. This reaction tends to react with independent alkenes, while It does not react with allyl alcohol (Formula 4)[5].

‘ICHNucleophilic addition of 2 Methyl iodide prepared from samarium metal [6] can react with aldehydes, ketones and enones, and magnesium reagents can also be used For this reaction (Equation 5)[7]. The aluminum reagent can also be used to replace the allyl alcohol hydroxyl group with iodomethyl, Et3Al, Et2AlCl, Et2AlOEt All can participate in this reaction (such as equation 6)[8].

(+)-trans-(2S,3S)-bis(diphenylphosphine)bicyclo[2.2.1]hept-5-ene

Nucleophilic addition of ‘I2CH’ CH2I2 deprotonates under the action of a base After oxidation, I2CHM derivatives are obtained. These compounds are more stable than the corresponding ICH2M and can react with many electrophiles[9]. Commonly used bases include Cy2NLi, NaHMDS, LiHMDS and LDA. Allyl iodide is synthesized using I2CHLi. First treat diiodomethane with LiHMDS, then add sulfone, and evaporate the water to obtain allyl iodide, but the selectivity is relatively poor (Formula 7)[9].

Free radical addition Addition of ICH2 fragments to α,β-unsaturated ketones in the presence of triethylborane Reaction to obtainγ-iodoketone (formula 8)[10]. The intermediate boron enolate can be either hydrolyzed or alkylated.

Alkylation reaction The application of diiodomethane in alkylation is limited. ClCH2I and ClCH2Br are more prone to alkylation reactions than diiodomethane, but , diiodomethane can be used in cycloalkylation reactions. Diamine can react with diiodomethane. Slowly adding diiodomethane solution to the diamine solution can obtain a higher yield (Formula 9)[11]. In the reaction with Pt as a catalyst, diiodomethane reacts with thiol to obtain dithiane[12]. In addition, the in-situ generation of iodomethyllithium in the presence of diiodomethane and alkyl lithium can easily and quickly convert many carbonyl compounds into epoxides (Formula 10)[13].

3. Used in organic synthesis and Separation of mixed minerals. [33]

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BDMAEE:Bis (2-Dimethylaminoethyl) Ether

CAS NO:3033-62-3

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