25559-56-2

Basic information

• Product Name: Benzenepropanamide, a-methyl-b-oxo-N-phenyl-
• CAS NO: 25559-56-2
• Molecular Formula: C16H15NO2
• Molecular Weight: 253.301
• Mol File: 25559-56-2.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: Benzenepropanamide, a-methyl-b-oxo-N-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenepropanamide, a-methyl-b-oxo-N-phenyl-(25559-56-2)
• EPA Substance Registry System: Benzenepropanamide, a-methyl-b-oxo-N-phenyl-(25559-56-2)

Safety Data

• Hazardous Substances Data: 25559-56-2(Hazardous Substances Data)

Upstream product

• 103-71-9 phenyl isocyanate 
• 62-53-3 aniline 
• 10488-87-6 ethyl 2-benzoylpropionate 
• 14088-57-4 2-diazo-1-phenyl-1-propanone 
• 201230-82-2 carbon monoxide 
• 66981-69-9 2-(Dimethyl-λ⁴-sulfanylidene)-1-phenyl-propan-1-one 
• 622-37-7 Phenyl azide 
• 99408-66-9 3,5-diphenyl-4-aza-2,4-heptadiene 
• 116916-23-5 2-methyl-3-(1-phenylpropylamino)-N,3-diphenylprop-2-enamide 
• 1450-07-3 1-benzoylethylidenetriphenylphosphorane 
• 93-55-0 1-phenyl-propan-1-one 
• 124982-28-1 3-methyl-N-phenyl-4-phenyl-2,4-dioxobutyramide 
• 29047-30-1 α-Methyl-β-methylthiomethoxy-β-phenylacryl-anilid 
• 959-66-0 3-oxo-3-phenylpropionanilide 

Downstream Products

• 93-89-0 benzoic acid ethyl ester 
• 111528-58-6 2-methyl-3-phenyl-3-propoxy-acrylic acid anilide 
• 620-71-3 N-(phenyl)-2-methylacetamide 
• 65-85-0 benzoic acid 
• 1422194-20-4 C₁₆H₁₅NO₃ 
• 37118-75-5 3-methyl-4-phenyl-2-quinolinone 

Relevant articles and documents

Unique features of chiral palladium enolates derived from β-ketoamide: structure and catalytic asymmetric Michael and fluorination reactions

Abstract We have previously reported enantioselective reactions of 1,3-diketones and β-ketoesters with various electrophiles catalyzed by chiral Pd complex, in which chiral Pd enolates play a key role. Here, we present a detailed examination of Pd-catalyz

Enantioselective α-hydroxylation of -ketoamides

The first enantioselective α-hydroxylation reaction of α-substituted -ketoamides has been developed by using the commercially available hydroquinine/TBHP system. The tertiary alcohols are obtained in good to high yield and up to 83% ee, which can be improved by a single crystallization.

A NEW METHOD FOR SYNTHESIS OF N-ARYL-2-BENZOYLPROPIONAMIDES

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