85793-69-7

Basic information

• Product Name: Benzoic acid, 2-[(2-methoxy-2-oxoethyl)phenylamino]-, methyl ester
• CAS NO: 85793-69-7
• Molecular Formula: C17H17NO4
• Molecular Weight: 299.326
• Mol File: 85793-69-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 2-[(2-methoxy-2-oxoethyl)phenylamino]-, methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 2-[(2-methoxy-2-oxoethyl)phenylamino]-, methyl ester(85793-69-7)
• EPA Substance Registry System: Benzoic acid, 2-[(2-methoxy-2-oxoethyl)phenylamino]-, methyl ester(85793-69-7)

Safety Data

• Hazardous Substances Data: 85793-69-7(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 85793-68-6 2-<(carboxymethyl)phenylamino>benzoic acid 
• 74-88-4 methyl iodide 
• 16095-32-2 1-phenyl-1,2-dihydro-4H-benzo[d][1,3]oxazin-4-one 
• 91-40-7 2-(phenylamino)benzoic acid 

Downstream Products

• 89224-57-7 3-ethoxy-7-methoxy-4-phenyl-4H-furo<3,2-b>indole-2-carboxylic acid methyl ester 
• 89224-69-1 3-ethoxy-7-methoxy-4-phenyl-4H-furo<3,2-b>indole-2-carboxylic acid 
• 89224-61-3 3-ethoxy-4-phenyl-4H-furo<3,2-b>indole-2-carboxylic acid methyl ester 
• 89224-60-2 3-methoxy-4-phenyl-4H-furo<3,2-b>indole-2-carboxylic acid methyl ester 
• 89224-85-1 3-ethoxy-4-phenyl-4H-furo[3,2-b]indole-2-carboxamide 
• 89224-83-9 3-ethoxy-4-phenyl-4H-furo[3,2-b]indole-2-carboxylic acid 
• 89224-58-8 3-(2-methoxy-2-oxoethoxy)-1-phenyl-1H-indole-2-carboxylic acid methyl ester 
• 89224-80-6 3-methoxy-4-phenyl-4H-furo<3,2-b>indole-2-carboxamide 
• 89224-62-4 3-methoxy-4-phenyl-4H-furo<3,2-b>indole-2-carboxylic acid 
• 93424-84-1 3-hydroxy-4-phenyl-4H-furo<3,2-b>indole-2-carboxylic acid methyl ester 
• 131540-79-9 1-phenyl-3-piperazino-1H-indole 
• 71711-33-6 3-hydroxy-1-phenyl-1H-indole-2-carboxylic acid methyl ester 

Relevant articles and documents

Organocatalytic enantioselective amination of 2-substituted indolin-3-ones: A strategy for the synthesis of chiral α-hydrazino esters

An efficient enantioselective α-amination of 2-substituted 3-indolinones has been achieved for the first time using hydroquinidine as a chiral catalyst through an aza-Michael reaction. The desired α-hydrazino esters are obtained in excellent yields with h

Indole Esters as Heterocyclic Synthons. III . Preparation and Reactions of Furoindoles

The preparation of furoindoles via Dieckmann cyclization is described.The precursor diesters were obtained from 3-hydroxy-1H-indole-2-carboxylic acid esters and methyl or ethyl bromoacetate.Reactions of the furoindole enolic esters prepared