1019019-27-2

Basic information

• Product Name: 2-Hydroxy-2-p-tolyl-acetimidic acid ethyl ester
• CAS NO: 1019019-27-2
• Molecular Weight: 193.246
• Mol File: 1019019-27-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-Hydroxy-2-p-tolyl-acetimidic acid ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Hydroxy-2-p-tolyl-acetimidic acid ethyl ester(1019019-27-2)
• EPA Substance Registry System: 2-Hydroxy-2-p-tolyl-acetimidic acid ethyl ester(1019019-27-2)

Safety Data

• Hazardous Substances Data: 1019019-27-2(Hazardous Substances Data)

Upstream product

• 104-87-0 4-methyl-benzaldehyde 
• 64-17-5 ethanol 
• 4815-10-5 2-hydroxy-2-(4-methylphenyl)acetonitrile 

Downstream Products

• 116544-54-8 (2-Benzoyl-4-chloro-phenoxy)-p-tolyl-acetic acid ethyl ester 
• 116544-57-1 (6-Benzoyl-2,3-dimethyl-phenoxy)-p-tolyl-acetic acid ethyl ester 
• 116544-56-0 (2-Benzoyl-4,6-dimethyl-phenoxy)-p-tolyl-acetic acid ethyl ester 
• 116544-55-9 (2-Benzoyl-4-methyl-phenoxy)-p-tolyl-acetic acid ethyl ester 
• 116544-53-7 (2-Benzoyl-phenoxy)-p-tolyl-acetic acid ethyl ester 
• 116544-64-0 (2-Benzoyl-4-chloro-phenoxy)-p-tolyl-acetic acid 
• 116544-66-2 (2-Benzoyl-4,6-dimethyl-phenoxy)-p-tolyl-acetic acid 
• 116544-67-3 (6-Benzoyl-2,3-dimethyl-phenoxy)-p-tolyl-acetic acid 
• 116544-65-1 (2-Benzoyl-4-methyl-phenoxy)-p-tolyl-acetic acid 
• 116544-63-9 (2-Benzoyl-phenoxy)-p-tolyl-acetic acid 
• 116544-73-1 6,7-Dimethyl-3-phenyl-2-p-tolyl-benzofuran 
• 15674-78-9 (+/-)-α-bromo-p-tolylacetic acid ethyl ester 
• 16762-20-2 2-(4-methylphenyl)-3-phenylbenzo[b]furan 
• 55082-69-4 2-(4-methylphenyl)-3-phenyl-5-chlorobenzofuran 

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.