2,2,2-Trifluoroethanethioamide, with the CAS number 421-52-3, is an organic compound characterized by the presence of a thioamide functional group and three fluorine atoms attached to the ethyl backbone. This compound typically exhibits a high degree of polarity due to the electronegative fluorine atoms, which can influence its solubility in various solvents. The presence of the thioamide group imparts unique reactivity, making it a potential candidate for various chemical reactions, including nucleophilic substitutions and condensation reactions. Additionally, the trifluoromethyl group can enhance the compound's stability and alter its physical properties, such as boiling and melting points, compared to its non-fluorinated counterparts. In terms of safety, compounds containing fluorine and sulfur may pose specific hazards, necessitating careful handling and storage. Overall, 2,2,2-trifluoroethanethioamide is of interest in both synthetic organic chemistry and potential applications in pharmaceuticals or agrochemicals due to its unique structural features.

2,2,2-trifluoroethanethioamide

421-52-3: 2,2,2-Trifluoroethanethioamide, with the CAS number 421-52-3, is an organic compound characterized by the presence of a thioamide functional group and three fluorine atoms attached to the ethyl backbone. This compound typically exhibits a high degree of polarity due to the electronegative fluorine atoms, which can influence its solubility in various solvents. The presence of the thioamide group imparts unique reactivity, making it a potential candidate for various chemical reactions, including nucleophilic substitutions and condensation reactions. Additionally, the trifluoromethyl group can enhance the compound's stability and alter its physical properties, such as boiling and melting points, compared to its non-fluorinated counterparts. In terms of safety, compounds containing fluorine and sulfur may pose specific hazards, necessitating careful handling and storage. Overall, 2,2,2-trifluoroethanethioamide is of interest in both synthetic organic chemistry and potential applications in pharmaceuticals or agrochemicals due to its unique structural features.

CAS 421-52-3

2,2,2-trifluoroethanethioamide

2,2,2-Trifluoroethanethioamide

Ref: IN-DA0073MA

2,2,2-Trifluorothioacetamide

Ref: 54-PC401014

2,2,2-Trifluorothioacetamide

Ref: 10-F038321