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CAS 121307-80-0

:

6-(Trifluoromethyl)-2(1H)-pyridinethione

Description:
6-(Trifluoromethyl)-2(1H)-pyridinethione, with the CAS number 121307-80-0, is a chemical compound characterized by its pyridine ring structure substituted with a trifluoromethyl group and a thione functional group. The presence of the trifluoromethyl group enhances the compound's lipophilicity and can influence its reactivity and biological activity. The thione functional group, which is a sulfur-containing moiety, can participate in various chemical reactions, including nucleophilic attacks and coordination with metal ions. This compound may exhibit interesting properties such as potential antimicrobial or herbicidal activity, making it of interest in agricultural and pharmaceutical research. Its unique structure allows for various applications in synthetic chemistry, particularly in the development of new materials or biologically active compounds. As with many fluorinated compounds, it is essential to consider its environmental impact and stability under various conditions. Safety data sheets should be consulted for handling and storage guidelines, as well as potential hazards associated with its use.
Formula:C6H4F3NS
InChI:InChI=1S/C6H4F3NS/c7-6(8,9)4-2-1-3-5(11)10-4/h1-3H,(H,10,11)
InChI key:InChIKey=VIBIZDLLHPQBRV-UHFFFAOYSA-N
SMILES:C(F)(F)(F)C=1NC(=S)C=CC1
Synonyms:
  • 2(1H)-Pyridinethione, 6-(trifluoromethyl)-
  • 3-Fluoro-5-nitro-2-hydroxypyridine
  • 3-Fluoro-5-nitropyridin-2-ol
  • 5-Nitropyridin-2-ylboronic acid
  • 6-(4-Methoxybenzylcarbamoyl)pyridine-3-boronic acid
  • 6-(Trifluoromethyl)-2(1H)-pyridinethione
  • 6-(Trifluoromethyl)Pyridine-2-Thiol
  • 6-Trifluoromethyl-2-pyridinethiol
  • Methyl 2-hydroxy-3-nitro-5-pyridinecarboxylate
  • Methyl 6-hydroxy-5-nitronicotinate
  • N-4-Methoxybenzyl 5-borono-2-pyridinecarboxamide
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