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ChemicalBook--->CAS DataBase List--->87226-41-3

87226-41-3

87226-41-3 Structure

87226-41-3 Structure
IdentificationBack Directory
[Name]

RAK 593
[CAS]

87226-41-3
[Synonyms]

RAK 593
SDX 101
R-Etodolac
(-)-(R)-Etodolac
Etodolac Impurity 16
Etodolac Impurity 14 ((R)-(-)-Etodolac)
(R)-1,8-Diethyl-1,3,4,9-tetrahydropyrano[3,4-b]indole-1-acetic Acid
Pyrano[3,4-b]indole-1-acetic acid, 1,8-diethyl-1,3,4,9-tetrahydro-, (R)-
Pyrano[3,4-b]indole-1-acetic acid, 1,8-diethyl-1,3,4,9-tetrahydro-, (1R)-
[Molecular Formula]

C17H21NO3
[MDL Number]

MFCD00870722
[MOL File]

87226-41-3.mol
[Molecular Weight]

287.35
Chemical PropertiesBack Directory
[Melting point ]

136 - 140°C
[storage temp. ]

-20°C Freezer
[solubility ]

Chloroform (Sparingly), DMSO (Slightly) Methanol (Slightly)
[form ]

Solid
[color ]

White to Off-White
Safety DataBack Directory
[HS Code ]

9999999999
Hazard InformationBack Directory
[Uses]

The R-enantiomer of Etodolac (E933090). Anti-inflammatory; analgesic.
[Definition]

ChEBI: (R)-etodolac is the R-enantiomer of etodolac. It is inactive, in contrast to the enantiomer, (S)-etodolac, which is a preferential inhibitor of cyclo-oxygenase 2 and a non-steroidal anti-inflammatory. The racemate is commonly used for the treatment of rheumatoid arthritis and osteoarthritis, and for the alleviation of postoperative pain. It is an enantiomer of a (S)-etodolac.
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