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CAS 1208081-97-3

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2-Chloro-6-(trifluoromethyl)-3-pyridinesulfonamide

Description:
2-Chloro-6-(trifluoromethyl)-3-pyridinesulfonamide is a chemical compound characterized by its pyridine ring, which is substituted at the 2 and 6 positions with a chlorine atom and a trifluoromethyl group, respectively. The sulfonamide functional group is attached at the 3-position of the pyridine ring. This compound is typically a solid at room temperature and is known for its potential applications in medicinal chemistry, particularly in the development of pharmaceuticals. The presence of the trifluoromethyl group enhances lipophilicity and can influence biological activity, making it a subject of interest in drug design. Additionally, the sulfonamide moiety is known for its antibacterial properties, which may contribute to the compound's efficacy in various therapeutic contexts. Its molecular structure suggests that it may exhibit unique reactivity and interaction patterns due to the electronegative fluorine atoms and the sulfonamide group, which can participate in hydrogen bonding and other intermolecular interactions. Overall, this compound represents a valuable entity in the field of organic and medicinal chemistry.
Formula:C6H4ClF3N2O2S
InChI:InChI=1S/C6H4ClF3N2O2S/c7-5-3(15(11,13)14)1-2-4(12-5)6(8,9)10/h1-2H,(H2,11,13,14)
InChI key:InChIKey=NYYZQFIIBCYUED-UHFFFAOYSA-N
SMILES:C(F)(F)(F)C=1N=C(Cl)C(S(N)(=O)=O)=CC1
Synonyms:
  • 2-Chloro-6-(trifluoromethyl)-3-pyridinesulfonamide
  • 3-Pyridinesulfonamide, 2-chloro-6-(trifluoromethyl)-
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