159883-92-8

Basic information

• Product Name: [(R)-1-(2,2-diethoxyethyl)-2-oxo-3-(3-p-tolylureido)-2,3-dihydro-1H-indol-3-yl]acetic acid (1R,2S,5R)-2-isopropyl-5-methylcyclohexyl ester
• Synonyms: [(R)-1-(2,2-diethoxyethyl)-2-oxo-3-(3-p-tolylureido)-2,3-dihydro-1H-indol-3-yl]acetic acid (1R,2S,5R)-2-isopropyl-5-methylcyclohexyl ester
• CAS NO: 159883-92-8
• Molecular Weight: 593.764
• Mol File: 159883-92-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: [(R)-1-(2,2-diethoxyethyl)-2-oxo-3-(3-p-tolylureido)-2,3-dihydro-1H-indol-3-yl]acetic acid (1R,2S,5R)-2-isopropyl-5-methylcyclohexyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: [(R)-1-(2,2-diethoxyethyl)-2-oxo-3-(3-p-tolylureido)-2,3-dihydro-1H-indol-3-yl]acetic acid (1R,2S,5R)-2-isopropyl-5-methylcyclohexyl ester(159883-92-8)
• EPA Substance Registry System: [(R)-1-(2,2-diethoxyethyl)-2-oxo-3-(3-p-tolylureido)-2,3-dihydro-1H-indol-3-yl]acetic acid (1R,2S,5R)-2-isopropyl-5-methylcyclohexyl ester(159883-92-8)

Safety Data

• Hazardous Substances Data: 159883-92-8(Hazardous Substances Data)

Upstream product

• 107976-78-3 1H-indole-2,3-dione 3-(O-methyloxime) 
• 91-56-5 indole-2,3-dione 
• 159884-54-5 1-(2,2-diethoxyethyl)-1H-indole-2,3-dione 3-(O-methyloxime) 
• 195451-17-3 N-[1-(2,2-diethoxyethyl)-2,3-dihydro-2-oxo-1H-indol-3-yl]-N'-(4-methylphenyl)urea 
• 16832-20-5 (1R,2S,5R)-menthol bromoacetate 

Downstream Products

• 199800-49-2 AG 041R 
• 913191-67-0 [(R)-2-oxo-1-(2-oxo-ethyl)-3-(3-p-tolylureido)-2,3-dihydro-1H-indol-3-yl]-acetic acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester 
• 159884-50-1 [1-(2,2-diethoxy-ethyl)-2-oxo-3-(3-p-tolyl-ureido)-2,3-dihydro-1H-indol-3-yl]-acetic acid 

Relevant articles and documents

Efficient asymmetric synthesis of novel gastrin receptor antagonist AG-041R via highly stereoselective alkylation of oxindole enolates

An efficient method for asymmetric synthesis of the potent Gastrin/CCK-B receptor antagonist AG-041R was developed. Core oxindole stereochemistry was established by asymmetric alkylation of oxindole enolates with bromoacetic acid esters, using l-menthol a