5382-15-0

Basic information

• Product Name: Propanoic acid, 3-[(4-methoxyphenyl)amino]-3-oxo-, ethyl ester
• CAS NO: 5382-15-0
• Molecular Formula: C12H15NO4
• Molecular Weight: 237.255
• Mol File: 5382-15-0.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: Propanoic acid, 3-[(4-methoxyphenyl)amino]-3-oxo-, ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Propanoic acid, 3-[(4-methoxyphenyl)amino]-3-oxo-, ethyl ester(5382-15-0)
• EPA Substance Registry System: Propanoic acid, 3-[(4-methoxyphenyl)amino]-3-oxo-, ethyl ester(5382-15-0)

Safety Data

• Hazardous Substances Data: 5382-15-0(Hazardous Substances Data)

Upstream product

• 623-73-4 diazoacetic acid ethyl ester 
• 201230-82-2 carbon monoxide 
• 104-94-9 4-methoxy-aniline 
• 36239-09-5 ethyl chlorocarbonylacetate 
• 1010117-23-3 diethyl 2-nitro-3-oxopentanedioate 
• 105-50-0 diethyl 1,3-acetonedicarboxylate 
• 105-53-3 diethyl malonate 

Downstream Products

• 5507-39-1 2-(3-chloro-anilinomethylene)-N-(4-methoxy-phenyl)-malonamic acid ethyl ester 
• 1621689-59-5 (Z)-5-((6-(3-(4-methoxyphenylamino)-3-oxopropanamido)-2-oxoindolin-3-ylidene)methyl)-2,4-dimethyl-1H-pyrrole-3-carboxylic acid 
• 1474049-69-8 (Z)-N¹-(3-((1H-pyrrol-2-yl)methylene)-2-oxoindolin-6-yl)-N³-(4-methoxyphenyl)malonamide 
• 1621689-23-3 N¹-(4-methoxyphenyl)-N³-(2-oxoindolin-6-yl)malonamide 
• 1391914-13-8 ethyl 3-(4-methoxyphenylamino)-3-oxo-2,2-diphenylpropanoate 
• 1118541-81-3 3-[N-(4-methoxyphenyl)carbamoyl]-5-nitro-1-propylpyridin-2(1H)-one 
• 102021-96-5 4-p-anisidino-7-chloro-quinoline-3-carboxylic acid ethyl ester 
• 5570-84-3 7-chloro-4-(4-methoxy-anilino)-quinoline-3-carboxylic acid 
• 6059-31-0 7-chloro-N-(4-methoxyphenyl)quinolin-4-amine 
• 81099-86-7 4-[(7-chloroquinolin-4-yl)amino]phenol 

Relevant articles and documents

AlCl 3 -Mediated Synthesis of 4-Aryl-2-quinolone-3-carboxylates

4-Aryl-2-quinolones are important skeletons from both chemical and medicinal viewpoints. We herein report the development of an efficient synthetic method for 3-substituted 4-aryl-2-quinolones. The key reaction in this process involves an AlCl 3/sub

Carbene radicals in cobalt(II)-porphyrin-catalysed carbene carbonylation reactions; A catalytic approach to ketenes

One-pot radicals: Cobalt(III)-carbene radicals, generated by metallo-radical activation of diazo compounds and N-tosylhydrazone sodium salts with cobalt(II) complexes of porphyrins, readily undergo radical addition to carbon monoxide, allowing the catalytic production of ketenes. These ketenes subsequently react with various amines, alcohols and imines in one-pot tandem transformations to produce differently substituted amides, esters and β-lactams in good isolated yields. Copyright

Nucleophilic substitution accompanying carbon-carbon bond cleavage assisted by a nitro group

A 2-nitrated 3-oxoester reacted with amines or alcohols to afford unsymmetrical malonic acid derivatives as a result of nucleophilic substitution accompanying C-C bond cleavage. The 2-nitrated 3-oxoester easily formed ammonium salts with amines. When the amine is liberated from the salt under equilibrium, nucleophilic amine and electrophilic keto ester locate close to each other. This intimate pair effect causes a pseudo intramolecular reaction to occur, giving rise to effective substitution under mild conditions.