94797-02-1

Basic information

• Product Name: Benzoic acid, 4-methyl-, 2-benzoyl-4-chlorophenyl ester
• CAS NO: 94797-02-1
• Molecular Formula: C21H15ClO3
• Molecular Weight: 350.801
• Mol File: 94797-02-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 4-methyl-, 2-benzoyl-4-chlorophenyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 4-methyl-, 2-benzoyl-4-chlorophenyl ester(94797-02-1)
• EPA Substance Registry System: Benzoic acid, 4-methyl-, 2-benzoyl-4-chlorophenyl ester(94797-02-1)

Safety Data

• Hazardous Substances Data: 94797-02-1(Hazardous Substances Data)

Upstream product

• 15023-58-2 4-chlorophenyl 4-methylbenzoate 
• 98-88-4 benzoyl chloride 

Downstream Products

• 116544-54-8 (2-Benzoyl-4-chloro-phenoxy)-p-tolyl-acetic acid ethyl ester 
• 116544-64-0 (2-Benzoyl-4-chloro-phenoxy)-p-tolyl-acetic acid 
• 55082-69-4 2-(4-methylphenyl)-3-phenyl-5-chlorobenzofuran 
• 85-19-8 (5-chloro-2-hydroxyphenyl)phenylmethanone 
• 99-94-5 p-Toluic acid 

Relevant articles and documents

Cyclodeshydratation d'aryloxy-2 diaryl-1,2 ethanones en diaryl-2,3 benzofurannes. Influence de la substitution sur la competition entre deux chemins reactionnels

Many of the methods for synthesizing derivatives of 2,3-diaryl benzofurans imply cyclodehydration of 1,2-diaryl 2-aryloxyethanones, leading often to a mixture of two isomers which differ by the presence of the aryl substituent at positions C-2 or C-3 of benzofuran.This isomerisation is explained by a competition between two possible mechanisms.Either a direct electrophilic substitution or the intermediate formation of an α-acylcarbenium ion.This study deals with the competition as determined by the substitution of aryl groups in the initial substrate.Each 2,3-diarylbenzofuran was synthesized previously using an unambiguous method.