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CAS 175278-08-7

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2,3,4-trifluorobenzenesulphonyl chloride

Description:
2,3,4-Trifluorobenzenesulphonyl chloride is an organic compound characterized by the presence of a sulphonyl chloride functional group attached to a benzene ring that is substituted with three fluorine atoms at the 2, 3, and 4 positions. This compound is typically a colorless to pale yellow liquid or solid, depending on its purity and temperature. It is known for its reactivity, particularly due to the presence of the sulphonyl chloride group, which can participate in nucleophilic substitution reactions. The trifluoromethyl groups enhance the compound's electrophilicity and can influence its solubility and stability in various solvents. Additionally, the presence of fluorine atoms often imparts unique properties, such as increased lipophilicity and altered electronic characteristics, making it useful in various synthetic applications, including the preparation of pharmaceuticals and agrochemicals. However, it is also important to handle this compound with care due to its potential toxicity and reactivity with water, which can lead to the release of hydrochloric acid.
Formula:C6H2ClF3O2S
InChI:InChI=1/C6H2ClF3O2S/c7-13(11,12)4-2-1-3(8)5(9)6(4)10/h1-2H
InChI key:InChIKey=XFTDZYFHXRZLEF-UHFFFAOYSA-N
SMILES:S(Cl)(=O)(=O)C1=C(F)C(F)=C(F)C=C1
Synonyms:
  • 2,3,4-Trifluorobenzene-1-sulfonyl chloride
  • 2,3,4-Trifluorobenzenesulfonyl Chloride
  • Benzenesulfonyl chloride, 2,3,4-trifluoro-
  • 2,3,4-TRIFLUOROBENZENESULPHONYL CHLORIDE
  • BUTTPARK 44\07-12
  • Benzenesulfonyl chloride, 2,3,4-trifluoro-(9CI)
  • 2,3,4-Trifluorobenzenesulphonyl chloride 97%
  • 2,3,4-Trifluorobenzenesulphonylchloride97%
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