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CAS 175205-76-2

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2,6-Dichloro-4-(trifluoromethyl)benzenesulfonyl chloride

Description:
2,6-Dichloro-4-(trifluoromethyl)benzenesulfonyl chloride is an organosulfur compound characterized by the presence of a sulfonyl chloride functional group attached to a chlorinated aromatic ring. This compound features two chlorine atoms and a trifluoromethyl group on the benzene ring, which contribute to its reactivity and physical properties. It is typically a solid at room temperature and is known for its high reactivity, particularly in nucleophilic substitution reactions due to the presence of the sulfonyl chloride group. This makes it useful in organic synthesis, particularly for the introduction of sulfonyl groups into various substrates. The trifluoromethyl group enhances the compound's lipophilicity and can influence its biological activity. Safety precautions are necessary when handling this compound, as it can be corrosive and may release toxic gases upon decomposition. Overall, 2,6-Dichloro-4-(trifluoromethyl)benzenesulfonyl chloride is a valuable reagent in synthetic organic chemistry, particularly in the development of pharmaceuticals and agrochemicals.
Formula:C7H2Cl3F3O2S
InChI:InChI=1S/C7H2Cl3F3O2S/c8-4-1-3(7(11,12)13)2-5(9)6(4)16(10,14)15/h1-2H
InChI key:InChIKey=MRGIKDMKHORAMU-UHFFFAOYSA-N
SMILES:S(Cl)(=O)(=O)C1=C(Cl)C=C(C(F)(F)F)C=C1Cl
Synonyms:
  • 2,6-Dichloro-4-(Trifluoromethyl)Benzenesulfonyl Chloride
  • 2,6-Dichloro-4-(trifluoromethyl)benzene-1-sulfonyl chloride
  • 2,6-Dichloro-4-(trifluoromethyl)phenylsulfonyl chloride
  • 2,6-Dichloro-4-trifluoromethylbenzenesulfonyl chloride
  • Benzenesulfonyl chloride, 2,6-dichloro-4-(trifluoromethyl)-
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