63499-93-4

Basic information

• Product Name: N-(2-oxo-1-phenylpropyl)acetamide
• Synonyms: N-(2-oxo-1-phenylpropyl)acetamide
• CAS NO: 63499-93-4
• Molecular Weight: 191.23
• Mol File: 63499-93-4.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: N-(2-oxo-1-phenylpropyl)acetamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2-oxo-1-phenylpropyl)acetamide(63499-93-4)
• EPA Substance Registry System: N-(2-oxo-1-phenylpropyl)acetamide(63499-93-4)

Safety Data

• Hazardous Substances Data: 63499-93-4(Hazardous Substances Data)

Upstream product

• 2835-06-5 phenylglycin 
• 103-79-7 1-phenyl-acetone 
• 4436-22-0 1-phenylpropylene oxide 
• 24175-87-9 2-acetoxy-1-phenyl-1propene 
• 10573-32-7 β-methoxy-β-methylstyrene 
• 108-24-7 acetic anhydride 
• 110-86-1 pyridine 

Downstream Products

• 77086-71-6 3-acetamido-3-phenyl-3-(Octa-2',7'-dienyl)propan-2-one 
• 77086-72-7 N-((3E,8E)-1-Acetyl-5-but-3-enyl-1-phenyl-trideca-3,8,12-trienyl)-acetamide 
• 32187-27-2 1-amino-1-phenylpropan-2-one 
• 20662-92-4 2,5-dimethyl-4-phenyloxazole 

Relevant articles and documents

Catalytic transformation of esters of 1,2-azido alcohols into α-amido ketones

The esters of 1,2-azido alcohols were transformed into α-amido ketones without external oxidants through the Ru-catalyzed formation of N-H imines with the liberation of N2 followed by intramolecular migration of the acyl moiety. A wide range of α-amido ketones were obtained, and one-pot transformation into the corresponding oxazoles (or a thiazole) was demonstrated.

NOUVELLE METHODE DE PREPARATION DE CETONES, ESTER ET NITRILE BENZYLIQUES α-FLUORES OU α,α-DIFLUORES

By anodic oxidation in CH3CN/Et3N, 3HF benzylic ketones, ester and nitrile yield specifically corresponding monofluoro or difluoro compounds.The reaction proceeds through an α-carbonyl or an α-cyano carbocation.