1236874-98-8

Basic information

• Product Name: 2,2,2-trifluoro-N-(4-iodophenyl)ethanethioamide
• Synonyms: 2,2,2-trifluoro-N-(4-iodophenyl)ethanethioamide
• CAS NO: 1236874-98-8
• Molecular Weight: 331.1
• Mol File: 1236874-98-8.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2,2,2-trifluoro-N-(4-iodophenyl)ethanethioamide(CAS DataBase Reference)
• NIST Chemistry Reference: 2,2,2-trifluoro-N-(4-iodophenyl)ethanethioamide(1236874-98-8)
• EPA Substance Registry System: 2,2,2-trifluoro-N-(4-iodophenyl)ethanethioamide(1236874-98-8)

Safety Data

• Hazardous Substances Data: 1236874-98-8(Hazardous Substances Data)

Upstream product

• 354-58-5 1,1,1-Trichloro-2,2,2-trifluoroethane 
• 3381-47-3 N-benzylidene-4-iodoaniline 
• 102904-39-2 (E)-1-phenyl-N-(4-iodophenyl)methanimine 
• 1068660-05-8 4-iodophenyl trifluoroacetimidochloride 

Downstream Products

• 126063-08-9 2,2,2-trifluoro-N-(4-iodophenyl)acetamide 
• 1310569-28-8 bis(N-(p-iodophenyl)trifluoroacetimidoyl) disulfide 

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