2-Naphthylthiol

2-Naphthylthiol structural formula

2-Naphthylthiol structural formula

Structural formula

Business number 023R
Molecular formula C10H18S
Molecular weight 160.24
label

β-naphthalenethiophenol,

2-Naphthylthiol,

2-Naphthyl mercaptan,

Thio-2-naphthol (β),

C10H7SH

Numbering system

CAS number:91-60-1

MDL number:MFCD00004086

EINECS number:202-082-5

RTECS number:QK3930000

BRN number:636389

PubChem number:24889151

Physical property data

1. Character:Light yellow crystalline powder.


2. Density (g/mL,25/4): Undetermined


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


4. Melting point (ºC):81


5. Boiling point (ºC,Normal pressure):286


6. Boiling point (ºC, 1.33kpa):146.3


7. Refractive Index: Undetermined


8. Flash Point (ºC): Undetermined


9. Specific optical rotation (º): Undetermined


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


11. Vapor pressure (kPa,25ºC): Undetermined136.1


3. isotonic specific volume (90.2K):359.6


4. Surface Tension (dyne/cm):48.6


5. Polarizability10-24cm3):20.72

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: 1

4. Number of rotatable chemical bonds: 0

5. Number of tautomers: 3

6. Topological molecule polar surface area 1

7. Number of heavy atoms: 11

8. Surface charge: 0

9. Complexity: 133

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

Should be stored sealed in a cool and dark place.

Synthesis method

first2-Naphthol and dimethylaminothio Formyl chloride is prepared by reacting in the presence of a baseO-2 Naphthyl dimethylaminothiocarbamate, refined Heat to270-275℃, reaction45min. After cooling, add to the mixture of potassium hydroxide solution and ethylene glycol, and heat to reflux1h. After hydrochlorization, chloroform extraction, reduced imitation extraction, and vacuum distillation, you can obtain2-Naphthylthiol

Purpose

It is used as a regeneration activation agent in the rubber industry and is suitable for use at low temperatures. However, the activation effect is not as good as that of the mango disulfides, and the regeneration tape has an unpleasant smell. The general dosage is0.1-1.5% , this product can also be used as an antioxidant, plasticizer and intermediate for organic synthesis body. 2-Naphthothiol is toxic and can cause dermatitis and ulcers.

n'”>℃, reaction45min. After cooling, add the mixture of potassium hydroxide solution and ethylene glycol, Heated reflow1h. After hydrochlorization, chloroform extraction, reduced imitation extraction, and vacuum distillation, you can obtain 2-

Purpose

It is used as a regeneration activation agent in the rubber industry and is suitable for use at low temperatures. However, the activation effect is not as good as that of the mango disulfides, and the regeneration tape has an unpleasant smell. The general dosage is0.1-1.5% , this product can also be used as an antioxidant, plasticizer and intermediate for organic synthesis body. 2-Naphthothiol is toxic and can cause dermatitis and ulcers.

BDMAEE:Bis (2-Dimethylaminoethyl) Ether

CAS NO:3033-62-3

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