113975-83-0

Basic information

• Product Name: trans-1-ethyl-1,3,4,9-tetrahydro-4-(phenylmethyl)pyrano<3,4-b>indole-1-acetic acid methyl ester
• Synonyms: trans-1-ethyl-1,3,4,9-tetrahydro-4-(phenylmethyl)pyrano<3,4-b>indole-1-acetic acid methyl ester
• CAS NO: 113975-83-0
• Molecular Weight: 363.456
• Mol File: 113975-83-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: trans-1-ethyl-1,3,4,9-tetrahydro-4-(phenylmethyl)pyrano<3,4-b>indole-1-acetic acid methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: trans-1-ethyl-1,3,4,9-tetrahydro-4-(phenylmethyl)pyrano<3,4-b>indole-1-acetic acid methyl ester(113975-83-0)
• EPA Substance Registry System: trans-1-ethyl-1,3,4,9-tetrahydro-4-(phenylmethyl)pyrano<3,4-b>indole-1-acetic acid methyl ester(113975-83-0)

Safety Data

• Hazardous Substances Data: 113975-83-0(Hazardous Substances Data)

Upstream product

• 1589-82-8 phenylmagnesium bromide 
• 111479-02-8 1-ethyl-4-hydroxy-1,3,4,9-tetrahydropyrano<3,4-b>indole-1-acetic acid methyl ester 
• 103-25-3 3-phenylpropanoic acid methyl ester 
• 100-44-7 benzyl chloride 
• 111503-75-4 4-amino-1-ethyl-1,3,4,9-tetrahydropyrano<3,4-b>indole-1-acetic acid methyl ester 
• 113996-90-0 methyl 2,3-dihydro-3-hydroxy-2-oxo-α-(phenylmethyl)-1H-indole-3-acetate 
• 113975-70-5 methyl α-(phenylmethyl)indole-3-acetate 
• 113975-78-3 β-amino-O,N-diformylindole-3-ethanol 
• 113975-79-4 β-formamidoindole-3-ethanol 
• 91566-74-4 α-aminoindole-3-acetic acid ethyl ester 
• 57115-38-5 α-(phenylmethyl)indole-3-acetic acid 
• 34951-73-0 β-aminoindole-3-ethanol 
• 91-56-5 indole-2,3-dione 
• 91393-10-1 ethyl 3-indoleglyoxylate oxime 

Downstream Products

• 113975-74-9 trans-1-ethyl-1,3,4,9-tetrahydro-4-(phenylmethyl)pyrano<3,4-b>indole-1-acetic acid 

Relevant articles and documents

Synthesis and Analgesic Activity of Pemedolac (cis-1-Ethyl-1,3,4,9-tetrahydro-4-(phenylmethyl)pyranoindole-1-acetic Acid)

The synthesis of cis-1-ethyl-1,3,4,9-tetrahydro-4-(phenylmethyl)pyranoindole-1-acetic acid, pemedolac (USAN), is described.This compound has been found to be a potent analgesic agent in primary screening.Pemedolac has been resolved and the active (+)-enantiomer assigned a 1S,4R absolute configuration on the basis of a crystallographic analysis of its (S)-(-)-borneol ester.