85635-61-6

Basic information

• Product Name: 2-Butenamide, 2-hydroxy-4-oxo-N,4-diphenyl-
• CAS NO: 85635-61-6
• Molecular Formula: C16H13NO3
• Molecular Weight: 267.284
• Mol File: 85635-61-6.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 2-Butenamide, 2-hydroxy-4-oxo-N,4-diphenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Butenamide, 2-hydroxy-4-oxo-N,4-diphenyl-(85635-61-6)
• EPA Substance Registry System: 2-Butenamide, 2-hydroxy-4-oxo-N,4-diphenyl-(85635-61-6)

Safety Data

• Hazardous Substances Data: 85635-61-6(Hazardous Substances Data)

Upstream product

• 68728-37-0 5-phenyl-2,3-dihydrofurandione 
• 62-53-3 aniline 
• 20577-73-5 methyl 4-phenyl-2,4-dioxobutanoate 
• 113416-21-0 methyl ester of 4-phenyl-2-phenylamino-4-oxo-2-butenoic acid 
• 55991-67-8 5-phenylfuran-2,3-dione 

Downstream Products

• 118081-87-1 N-phenyl-β-diphenylmethylbenzoylpyruvamide 

Relevant articles and documents

Acylpyruvic acid amides and hydrazides: XII. Reaction of 4-Aryl-2-hydroxy-4-oxo-2-butenic acids arylamides with triphenylphosphoranylideneacetic acid esters

4-Aryl-2-hydroxy-4-oxo-2-butenic (aroylpyruvic) acid arylamides react with triphenylphosphoranylidenacetic acid esters to form products of Wittig reaction at α-carbonyl group, the 5-aryl-3-arylaminocar-bonyl-5-oxo-3-pentenoic acid esters. Features in stru

Reaction of 5-Aryl-2,3-dihydro-2,3-furandiones with Esters of β-Aminocrotonic and 2-Arylamino-4-oxo-2-butenoic Acids

Ethyl 3-benzylaminocrotonate combines with 5-aryl-2,3-dihydro-2,3-furandiones as C- and N-nucleophiles by two competitive routes to give 2-aroylmethyl-1-benzyl-4-ethoxycarbonyl-2-hydroxy-5-methyl-2,3-dihydro-3- pyrrolones and benzylamides of aroylpyruvic acids. Methyl 4-aryl-2-arylamino-4-oxo-2-butenoates react with 5-aryl-2,3-dihydro-2,3-furandiones to yield only arylamides of aroylpyruvic acids.

CHEMISTRY OF OXALYL DERIVATIVES OF METHYL KETONES. XLIII. BIFUNCTIONAL CATALYSIS BY CARBOXYLIC ACIDS IN THE OPENING OF THE RING OF 5-ARYL-2,3-DIHYDROFURAN-2,3-DIONES BY THE ACTION OF ANILINE AND N-METHYLANILINE. EFFECT OF SUBSTITUENTS IN THE CATALYST AND

The kinetics of the reactions of 5-aryl-2,3-dihydrofuran-2,3-diones with aniline and N-methylaniline in toluene, catalyzed by carboxylic acids, were studied.By analysis of the dependence of the reaction rate on the nature of the substituents in the carbox