S-Etodolac Chemical Properties

Melting point:

>133°C (dec.)

storage temp. 

-20°C Freezer

solubility 

Chloroform (Sparingly), DMSO (Slightly), Methanol (Slightly)

form 

Solid

color 

White to Off-White

Safety Information

HS Code 

9999999999

S-Etodolac Usage And Synthesis

Uses

The S-enantiomer of Etodolac (E933090). Anti-inflammatory; analgesic.

Definition

ChEBI: (S)-etodolac is the S-enantiomer of etodolac. It is a preferential inhibitor of cyclo-oxygenase 2 and a non-steroidal anti-inflammatory, whereas the enantiomer, (R)-etodolac, is inactive. The racemate is commonly used for the treatment of rheumatoid arthritis and osteoarthritis, and for the alleviation of postoperative pain. It has a role as a cyclooxygenase 2 inhibitor and a non-narcotic analgesic. It is an enantiomer of a (R)-etodolac.

S-Etodolac(87249-11-4)Related Product Information

• 4-Oxo Etodolac
• RAK 802
• 1,8-Diethyl-1,3,4,9-tetrahydro-4-oxo-pyrano[3,4-b]indole-1-acetic Acid Methyl Ester
• Etodolac methyl ester
• N-Methyl Etodolac
• 1-PROPYL ETODOLAC
• 8-Methyl Etodolac
• 8-PROPYL ETODOLAC
• 7-Ethyl tryptophol
• rac Etodolac Acyl-β-D-glucuronide
• 8-Desethyl Etodolac
• RAK 593
• 1-ISOPROPYL ETODOLAC
• 6-Hydroxy Etodolac
• 1-Isopropyl Etodolac
• Ethyl2,5-dihydro-5-oxo-1-phenyl-1H-1,2,4-triazole-3-carboxylate
• Ethyl 4-[2-(5-Chloro-2-methoxybenzamido)ethyl]benzene Sulfonamide Carbamate
• ETHYL ([3-(METHYLTHIO)-1,2,4-THIADIAZOL-5-YLTHIO]METHYL) CYANOCARBONIMIDODITHIOATE