61881-11-6

Basic information

• Product Name: Ethanethioamide, 2,2,2-trifluoro-N-phenyl-
• CAS NO: 61881-11-6
• Molecular Formula: C8H6F3NS
• Molecular Weight: 205.204
• Mol File: 61881-11-6.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Ethanethioamide, 2,2,2-trifluoro-N-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanethioamide, 2,2,2-trifluoro-N-phenyl-(61881-11-6)
• EPA Substance Registry System: Ethanethioamide, 2,2,2-trifluoro-N-phenyl-(61881-11-6)

Safety Data

• Hazardous Substances Data: 61881-11-6(Hazardous Substances Data)

Upstream product

• 354-58-5 1,1,1-Trichloro-2,2,2-trifluoroethane 
• 538-51-2 benzylidene phenylamine 
• 1750-36-3 (E)-N-benzylidenebenzenamine 
• 61881-19-4 2,2,2-trifluoro-N-phenyl-acetimidoyl chloride 
• 81290-20-2 (trifluoromethyl)trimethylsilane 
• 103-72-0 phenyl isothiocyanate 
• 404-24-0 2,2,2-trifluoro-N-phenylacetamide 

Downstream Products

• 1225041-11-1 bis(N-phenyltrifluoroacetimidoyl) disulfide 
• 404-24-0 2,2,2-trifluoro-N-phenylacetamide 
• 14468-40-7 2-(trifluoromethyl)-1,3-benzothiazole 
• 61977-78-4 Methyl-N-phenyltrifluoracetimidat 
• 61881-19-4 2,2,2-trifluoro-N-phenyl-acetimidoyl chloride 
• 61881-21-8 N-Pentafluoraethylanilin 

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

Trifluoromethylation of heterocumulenes with trimethyl(trifluoromethyl)silane in the presence of fluoride ions: Synthesis of trifluoroacetamides and trifluorothioacetamides from isocyanates and isothiocyanates

Trimethyl(trifluoromethyl)silane reacts in the presence of fluoride ions with isocyanates and isothiocyanates under mild conditions to give corresponding trifluoroacetamides and trifluorothioacetamides in high yields.