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CAS 175277-51-7

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5-(Trifluoromethyl)-2-pyridinecarbothioamide

Description:
5-(Trifluoromethyl)-2-pyridinecarbothioamide is an organic compound characterized by the presence of a pyridine ring substituted with a trifluoromethyl group and a carbothioamide functional group. The trifluoromethyl group (-CF3) is known for its electron-withdrawing properties, which can significantly influence the compound's reactivity and stability. The carbothioamide functional group, which contains a sulfur atom bonded to a carbonyl and an amine, contributes to the compound's potential as a ligand in coordination chemistry and its utility in various synthetic applications. This compound may exhibit interesting biological activities due to its structural features, making it a subject of interest in medicinal chemistry. Additionally, its unique electronic properties can affect its solubility and interaction with other chemical species. Overall, 5-(Trifluoromethyl)-2-pyridinecarbothioamide is a versatile compound with potential applications in pharmaceuticals and agrochemicals, although specific properties such as melting point, boiling point, and solubility would require empirical data for precise characterization.
Formula:C7H5F3N2S
InChI:InChI=1S/C7H5F3N2S/c8-7(9,10)4-1-2-5(6(11)13)12-3-4/h1-3H,(H2,11,13)
InChI key:InChIKey=ORSQVELABPHSGL-UHFFFAOYSA-N
SMILES:C(F)(F)(F)C=1C=CC(C(N)=S)=NC1
Synonyms:
  • 2-Pyridinecarbothioamide, 5-(trifluoromethyl)-
  • 3-Chloro-2-(Chloromethyl)-5-(Trifluoromethyl)Pyridine
  • 5-(Trifluoromethyl)-2-pyridinecarbothioamide
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