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CAS 39213-22-4

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3,5-Bis(trifluoromethyl)benzenesulfonamide

Description:
3,5-Bis(trifluoromethyl)benzenesulfonamide is an organic compound characterized by the presence of a sulfonamide functional group attached to a benzene ring that has two trifluoromethyl groups at the 3 and 5 positions. This structure imparts significant polarity and enhances the compound's reactivity. The trifluoromethyl groups are known for their electron-withdrawing properties, which can influence the compound's chemical behavior, making it useful in various applications, including pharmaceuticals and agrochemicals. The sulfonamide group contributes to its solubility in polar solvents and can participate in hydrogen bonding, affecting its interaction with biological systems. Additionally, the compound may exhibit unique thermal and chemical stability due to the presence of fluorine atoms, which can enhance its resistance to degradation. Overall, 3,5-Bis(trifluoromethyl)benzenesulfonamide is notable for its potential utility in synthetic chemistry and its role in the development of functional materials.
Formula:C8H5F6NO2S
InChI:InChI=1S/C8H5F6NO2S/c9-7(10,11)4-1-5(8(12,13)14)3-6(2-4)18(15,16)17/h1-3H,(H2,15,16,17)
InChI key:InChIKey=UQRLSJLFAHCJBF-UHFFFAOYSA-N
SMILES:C(F)(F)(F)C1=CC(C(F)(F)F)=CC(S(N)(=O)=O)=C1
Synonyms:
  • 3,5-Bis(trifluoromethyl)benzenesulfonamide
  • Benzenesulfonamide, 3,5-bis(trifluoromethyl)-
  • 3,5-Bis(trifluoromethyl)benzene-1-sulfonamide
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