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CAS 338422-71-2

:

4-[[3-Chloro-5-(trifluoromethyl)-2-pyridinyl]oxy]benzenesulfonyl chloride

Description:
4-[[3-Chloro-5-(trifluoromethyl)-2-pyridinyl]oxy]benzenesulfonyl chloride, with the CAS number 338422-71-2, is a chemical compound characterized by its sulfonyl chloride functional group, which is known for its reactivity and utility in organic synthesis. This compound features a pyridine ring substituted with a chlorine atom and a trifluoromethyl group, contributing to its unique electronic properties and potential biological activity. The presence of the benzenesulfonyl chloride moiety indicates that it can participate in nucleophilic substitution reactions, making it valuable in the synthesis of various pharmaceuticals and agrochemicals. Additionally, the trifluoromethyl group enhances lipophilicity and metabolic stability, which can influence the compound's pharmacokinetics. The compound is typically handled with care due to the reactivity of the sulfonyl chloride group, which can release hydrochloric acid upon reaction. Overall, this substance is of interest in medicinal chemistry and materials science for its potential applications in developing new chemical entities.
Formula:C12H6Cl2F3NO3S
InChI:InChI=1S/C12H6Cl2F3NO3S/c13-10-5-7(12(15,16)17)6-18-11(10)21-8-1-3-9(4-2-8)22(14,19)20/h1-6H
InChI key:InChIKey=NEQIUPPXYAOTSF-UHFFFAOYSA-N
SMILES:O(C1=C(Cl)C=C(C(F)(F)F)C=N1)C2=CC=C(S(Cl)(=O)=O)C=C2
Synonyms:
  • Benzenesulfonyl chloride, 4-[[3-chloro-5-(trifluoromethyl)-2-pyridinyl]oxy]-
  • 4-[[3-Chloro-5-(trifluoromethyl)-2-pyridinyl]oxy]benzenesulfonyl chloride
  • 4-(3-Chloro-5-trifluoromethylpyridin-2-yloxy)benzenesulfonyl chloride
  • 4-(3-Chloro-5-trifluoromethyl-2-pyridyloxy)benzenesulfonyl chloride
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