1310569-17-5

Basic information

• Product Name: 2,2,2-trifluoro-N-(2-methylphenyl)thioacetamide
• Synonyms: 2,2,2-trifluoro-N-(2-methylphenyl)thioacetamide
• CAS NO: 1310569-17-5
• Molecular Weight: 219.23
• Mol File: 1310569-17-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2,2,2-trifluoro-N-(2-methylphenyl)thioacetamide(CAS DataBase Reference)
• NIST Chemistry Reference: 2,2,2-trifluoro-N-(2-methylphenyl)thioacetamide(1310569-17-5)
• EPA Substance Registry System: 2,2,2-trifluoro-N-(2-methylphenyl)thioacetamide(1310569-17-5)

Safety Data

• Hazardous Substances Data: 1310569-17-5(Hazardous Substances Data)

Upstream product

• 354-58-5 1,1,1-Trichloro-2,2,2-trifluoroethane 
• 5877-55-4 N-benzylidene-2-methylaniline 
• 34143-86-7 N-((E)-benzylidene)-o-toluidine 
• 70314-81-7 2,2,2-trifluoro-N-(o-tolyl)acetimidoyl chloride 

Relevant articles and documents

Copper-catalyzed three component C[sbnd]S/C[sbnd]N coupling for the synthesis of trifluorothioacetamides

A copper-catalyzed three component C[sbnd]S/C[sbnd]N coupling reaction of imines with sulfur and CFC-113a was developed. The reaction involves amination and C[dbnd]S double bond formation of CFC-113a, leading to biologically important trifluorothioacetamides. The method features efficient construction of trifluorothioacetyl moiety from cheap sulfur and CFC-113a, and safe disposal for environmentally persistent Freon

Switching reaction pathways of trifluoromethylated thiobenzanilides by choice of different oxidative systems

Trifluoromethylated thiobenzanilides are efficiently converted to 2-trifluoromethylbenzothiazoles via intramolecular oxidative cyclization under CAN/NaHCO3 oxidation, while the dimerized products with "-S-S-" bond linkage are obtained when PIDA