Indomethacin Indomethacin
Structural formula
| Business number | 0164 |
|---|---|
| Molecular formula | C19H16ClNO4 |
| Molecular weight | 357.79 |
| label |
indomethacin, anti-inflammatory indoleic acid, 1-p-Chlorobenzoyl-5-methoxy-2-methylindoleacetic acid, Indenaxin, 1-(4-Chlorobenzoyl)-5-methoxy-2-methyl-3-indoleacetic acid |
Numbering system
CAS number:53-86-1
MDL number:MFCD00057095
EINECS number:200-186-5
RTECS number:NL3500000
BRN number:497341
PubChem number:24278173
Physical property data
1. Character:White crystal. Sensitive to light.
2. Density (g/mL,25/4℃): Undetermined
3. Relative vapor density (g/mL,AIR=1): Undetermined
4. Melting point (ºC):155℃（162℃）
5. Boiling point (ºC,Undetermined
6. Boiling point (ºC,5.2kPa): Undetermined
7. Refractive index: undetermined
8. Flashpoint (ºC): Undetermined
9. Specific optical rotation (º): Undetermined
10. Autoignition point or ignition temperature (ºC): Undetermined
11. 2. Molar volume (m3/mol) ：269.5
3. isotonic ratio(90.2K)：707.6
4. Surface Tension(dyne/cm)：47.4
5. Polarizability(10-24cm3)：37.49
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: 4
5. Number of tautomers: none
6. Topological molecule polar surface area 68.5
7. Number of heavy atoms: 25
8. Surface charge: 0
9. Complexity: 506
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
This product should be sealed in4Preserve dry.
Synthesis method
Indomethacin is obtained by diazotization, reduction, acidification, hydrolysis and cyclization of p-aminoanisole.
Purpose
For biochemical research. Biosynthesis of prostaglandins. The It is an anti-inflammatory product with obvious antipyretic effects. It is mainly used for rheumatic arthritis, ankylosing spondylitis, osteoarthritis, etc. that are intolerant to salicylic acid drugs or have insignificant efficacy.
“>P-aminoanisole undergoes diazotization, reduction, acidification, hydrolysis and cyclization to obtain indomethacin.
Purpose
For biochemical research. Biosynthesis of prostaglandins. The It is an anti-inflammatory product with obvious antipyretic effects. It is mainly used for rheumatic arthritis, ankylosing spondylitis, osteoarthritis, etc. that are intolerant to salicylic acid drugs or have insignificant efficacy.
