15206-97-0

Basic information

• Product Name: Ethyl α-acetyl-β-anilino-β-phenylpropionate
• Synonyms: Ethyl α-acetyl-β-anilino-β-phenylpropionate
• CAS NO: 15206-97-0
• Molecular Weight: 311.381
• Mol File: 15206-97-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Ethyl α-acetyl-β-anilino-β-phenylpropionate(CAS DataBase Reference)
• NIST Chemistry Reference: Ethyl α-acetyl-β-anilino-β-phenylpropionate(15206-97-0)
• EPA Substance Registry System: Ethyl α-acetyl-β-anilino-β-phenylpropionate(15206-97-0)

Safety Data

• Hazardous Substances Data: 15206-97-0(Hazardous Substances Data)

Upstream product

• 620-80-4 ethyl 2-benzylidene acetoacetate 
• 62-53-3 aniline 
• 141-97-9 ethyl acetoacetate 
• 538-51-2 benzylidene phenylamine 

Downstream Products

• 53295-33-3 ethyl 2,6-bis-phenyl-1-phenyl-4-phenylamino-1,2,5,6-tetrahydropyridine-3-carboxylate 
• 53219-37-7 diethyl 1,4-dihydro-2,6-dimethyl-1,4-diphenyl-3,5-pyridinedicarboxylate 
• 141-97-9 ethyl acetoacetate 
• 102-07-8 bis(diphenyl)urea 
• 538-51-2 benzylidene phenylamine 

Relevant articles and documents

1-ARYL- AND 1-BENZYL-3,5-DIETHOXYCARBONYL-1,4-DIHYDROPYRIDINES

The possibility has been studied of using anilines in the Hantzsch synthesis.It has been shown that, with the exception of those containing strong electron-accepting substituents, they take part in this reaction with the formation of 1-aryl-1,4-dihydropyridines.The reaction largely depends on the nature of the substituents in the aniline and in the benzaldehyde and is promoted by electron-accepting substituents in the aldehyde and electron-donating substituents in the amine.The mechanism of the reaction is discussed.A number of 1-benzyl-1,4-dihydroxypyridines have been synthesized.The UV, IR, and PMR spectra and the electro-oxidation of the compounds obtained have been studied.