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CAS 1208081-23-5

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2-Chloro-6-(trifluoromethyl)-3-pyridinesulfonyl chloride

Description:
2-Chloro-6-(trifluoromethyl)-3-pyridinesulfonyl chloride is a chemical compound characterized by its pyridine ring structure, which is substituted at the 2 and 6 positions with a chlorine atom and a trifluoromethyl group, respectively. The presence of the sulfonyl chloride functional group enhances its reactivity, making it a valuable intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. This compound is typically a solid at room temperature and is known for its strong electrophilic nature due to the sulfonyl chloride moiety, which can readily participate in nucleophilic substitution reactions. It is important to handle this substance with care, as it can be corrosive and may release toxic gases upon decomposition. Additionally, its trifluoromethyl group contributes to its lipophilicity, potentially influencing its biological activity and solubility in organic solvents. Overall, 2-Chloro-6-(trifluoromethyl)-3-pyridinesulfonyl chloride is a significant compound in synthetic chemistry with diverse applications.
Formula:C6H2Cl2F3NO2S
InChI:InChI=1S/C6H2Cl2F3NO2S/c7-5-3(15(8,13)14)1-2-4(12-5)6(9,10)11/h1-2H
InChI key:InChIKey=ZFGVQLINMYOUSU-UHFFFAOYSA-N
SMILES:C(F)(F)(F)C=1N=C(Cl)C(S(Cl)(=O)=O)=CC1
Synonyms:
  • 2-Chloro-6-(trifluoromethyl)-3-pyridinesulfonyl chloride
  • 3-Pyridinesulfonyl chloride, 2-chloro-6-(trifluoromethyl)-
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