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CAS 351003-49-1

:

5-Chloro-2-fluorobenzenesulfony1 Chloride

Description:
5-Chloro-2-fluorobenzenesulfonyl chloride is an organic compound characterized by the presence of a sulfonyl chloride functional group attached to a benzene ring that is substituted with both chlorine and fluorine atoms. This compound typically appears as a colorless to pale yellow liquid or solid, depending on its form and purity. It is known for its reactivity, particularly due to the sulfonyl chloride group, which can participate in nucleophilic substitution reactions, making it useful in the synthesis of various pharmaceuticals and agrochemicals. The presence of chlorine and fluorine substituents on the benzene ring can influence the compound's electronic properties and reactivity, enhancing its utility in chemical transformations. Additionally, it is important to handle this compound with care, as sulfonyl chlorides can be corrosive and may release toxic gases upon reaction with water or other nucleophiles. Proper safety precautions should be observed when working with this substance in a laboratory setting.
Formula:C6H3Cl2FO2S
InChI:InChI=1/C6H3Cl2FO2S/c7-4-1-2-5(9)6(3-4)12(8,10)11/h1-3H
InChI key:InChIKey=OZKAHSNNKADHTK-UHFFFAOYSA-N
SMILES:S(Cl)(=O)(=O)C1=C(F)C=CC(Cl)=C1
Synonyms:
  • 2-Fluoro-5-chlorobenzenesulfonyl chloride
  • 5-Chloro-2-Fluorobenzenesulfonyl Chlori
  • 5-Chloro-2-Fluorobenzenesulfonyl Chloride
  • 5-Chloro-2-Fluorobenzenesulphonyl Chloride
  • 5-Chloro-2-Fluorobenzensulfonyl Chloride
  • 5-Chloro-2-Fluorobenzensulphonyl Chloride
  • 5-Chloro-2-fluorobenzene-1-sulfonyl chloride
  • Benzenesulfonyl chloride, 5-chloro-2-fluoro-
  • Benzenesulfonyl chloride, 5-chloro-2-fluoro- (9CI)
  • (3-PHENYL-5-ISOXAZOL)METHANOL
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