152532-13-3

Basic information

• Product Name: N-(2,5-dimethoxyphenyl)-3-phenyl-3-oxopropionamide
• Synonyms: N-(2,5-dimethoxyphenyl)-3-phenyl-3-oxopropionamide
• CAS NO: 152532-13-3
• Molecular Weight: 299.326
• Mol File: 152532-13-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: N-(2,5-dimethoxyphenyl)-3-phenyl-3-oxopropionamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2,5-dimethoxyphenyl)-3-phenyl-3-oxopropionamide(152532-13-3)
• EPA Substance Registry System: N-(2,5-dimethoxyphenyl)-3-phenyl-3-oxopropionamide(152532-13-3)

Safety Data

• Hazardous Substances Data: 152532-13-3(Hazardous Substances Data)

Upstream product

• 94-02-0 ethyl 3-oxo-3-phenylpropionate 
• 102-56-7 2,5-dimethoxyaniline 

Downstream Products

• 1315268-30-4 3-benzoyl-1-(2,5-dimethoxyphenyl)-2-oxo-2,4-dihydro-1H-pyrrolo[2,3-b]quinoxaline-6-carboxylic acid 
• 1315268-29-1 3-benzoyl-1-(2,5-dimethoxyphenyl)-2-oxo-2,4-dihydro-1H-pyrrolo[2,3-b]quinoxaline-7-carboxylic acid 
• 1315268-23-5 3-benzoyl-7-methyl-1-(2,5-dimethoxyphenyl)-1,4-dihydropyrrolo[2,3-b]quinoxalin-2(4H)-one 
• 1315268-24-6 3-benzoyl-6-methyl-1-(2,5-dimethoxyphenyl)-1,4-dihydropyrrolo[2,3-b]quinoxalin-2(4H)-one 
• 1073059-11-6 1-(2,5-dimethoxyphenyl)-4-(phenyl(hydroxy)lmethylidene)pyrrolidine-2,3,5-trione 
• 1073059-12-7 3-benzoyl-1-(2,5-dimethoxyphenyl)-1,4-dihydropyrrolo[2,3-b]quinoxalin-2(4H)-one 
• 1073059-17-2 3-benzoyl-1-(2,5-dimethoxyphenyl)-1,4-dihydro-2H-pyrido[2,3-b]pyrrolo[2,3-e]pyrazin-2-one 
• 152532-07-5 1-Ethyl-5,8-dimethoxy-4-phenyl-1H-quinolin-2-one 
• 152532-02-0 5,8-Dimethoxy-1-methyl-4-phenyl-1H-quinolin-2-one 
• 152532-27-9 2-Ethoxy-5,8-dimethoxy-4-phenyl-quinoline 
• 152532-22-4 2,5,8-Trimethoxy-4-phenyl-quinoline 
• 152531-93-6 5,8-Dimethoxy-4-phenyl-1H-quinolin-2-one 
• 121848-86-0 2-(4-diethylamino-2-methyl-phenylimino)-3-oxo-3-phenyl-propionic acid-(2,5-dimethoxy-anilide) 

Relevant articles and documents

Efficient regioselective heterocyclisation leading to fluorescent fused pyrazine derivatives

The regioselective syntheses of substituted pyrrolo[2,3-b]quinoxaline, pyrido[2,3-b]pyrrolo[2,3-e]pyrazine, pyrido[2,3-b]pyrrolo[3,2-e]pyrazine and pyrido[3,4-b]pyrrolo[3,2-e]pyrazine are reported. Differential reactivity between two amino groups in ortho-diaminopyridine can be exploited to obtain new regio-defined unsymmetrical pyridopyrrolopyrazine derivatives. Weak electron-donating methyl or moderately electron-withdrawing carboxylic groups attached to the aromatic ortho-diamines reduce the regioselectivity of obtaining unsymmetrical substituted pyrrolo[2,3-b]quinoxaline. The fluorescence properties of the resultant 1-alkyl pyridopyrrolopyrazine and substituted pyrrolo[2,3-b]quinoxaline derivatives are presented.

SYNTHESIS OF 2(1H)-QUINOLINONEQUINONES AND 2-ALKOXYQUINOLINEQUINONES USING OXIDATIVE DEMETHYLATION WITH CERIUM (IV) AMMONIUM NITRATE

2,5,8(1H)-Quinolinetriones (12), 2,5,6(1H)-quinolinetriones (13), 2-alkoxy-5,8-quinolinediones (14), 2,8-dimethoxy-5,6-quinolinedione (15), and 2,6-dimethoxy-7,8-quinolinediones (16) were synthesized by oxidative demethylation of the corresponding 2(1H)-q