322-28-1

Basic information

• Product Name: N-(1-(4-fluorophenyl)-1-oxopropan-2-yl)acetamide
• CAS NO: 322-28-1
• Molecular Weight: 209.22
• Mol File: 322-28-1.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: N-(1-(4-fluorophenyl)-1-oxopropan-2-yl)acetamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(1-(4-fluorophenyl)-1-oxopropan-2-yl)acetamide(322-28-1)
• EPA Substance Registry System: N-(1-(4-fluorophenyl)-1-oxopropan-2-yl)acetamide(322-28-1)

Safety Data

• Hazardous Substances Data: 322-28-1(Hazardous Substances Data)

Upstream product

• 699-01-4 1-fluoro-4-(prop-1-en-1-yl)benzene 
• 118887-59-5 2-Azido-1-(4-fluoro-phenyl)-propan-1-ol 
• 118887-69-7 2-Bromo-1-(4-fluoro-phenyl)-propan-1-ol 
• 345-94-8 2-bromo-1-(4-fluorophenyl)propan-1-one 
• 456-03-1 1-(4-fluorophenyl)propan-1-one 
• 322-30-5 2-amino-1-(4-fluorophenyl)-1-propanone hydrochloride 
• 108-24-7 acetic anhydride 

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.