141474-47-7

Basic information

• Product Name: Acetamide, N-[2-chloro-6-(trifluoromethyl)phenyl]-
• CAS NO: 141474-47-7
• Molecular Formula: C9H7ClF3NO
• Molecular Weight: 237.609
• Mol File: 141474-47-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Acetamide, N-[2-chloro-6-(trifluoromethyl)phenyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Acetamide, N-[2-chloro-6-(trifluoromethyl)phenyl]-(141474-47-7)
• EPA Substance Registry System: Acetamide, N-[2-chloro-6-(trifluoromethyl)phenyl]-(141474-47-7)

Safety Data

• Hazardous Substances Data: 141474-47-7(Hazardous Substances Data)

Upstream product

• 88-17-5 2-(trifluoromethyl)benzenamine 
• 533-17-5 N-(2-chlorophenyl)acetamide 
• 2926-29-6 Langlois reagent 
• 361-17-1 N-(2-chloro-6-trifluoromethyl-phenyl)-phthalimide 
• 141474-38-6 2,4-Dichloro-6-trifluoromethyldiacetanilide 
• 433-94-3 2-chloro-6-(trifluoromethyl)benzenamine 

Relevant articles and documents

Visible-light-induced Pd-catalyzed: Ortho -trifluoromethylation of acetanilides with CF3SO2Na under ambient conditions in the absence of an external photocatalyst

A visible-light-induced Pd-catalyzed ortho-trifluoromethylation of acetanilides with CF3SO2Na was developed. The reaction proceeded smoothly at room temperature in air without any external photocatalyst or additive, providing the desired products in moderate to good yields with good functional group tolerance and regioselectivity.

Process for the selective reduction of the 4-halogen in 2,4-dihaloanilines

Substituted 2-haloanilines are prepared from the correspondingly substituted 2,4-dichloro- or 2,4-dibromoanilines by selectively reducing a chloro or bromo substituent para to a protected amino group in the presence of the same halogen as an ortho substit