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CS-W001157 4
Total: USD 88.00

2,3,4-Trifluorobenzenesulfonyl chloride

  • CAS No. 175278-08-7

  • Cat. No. CS-0132312
  • Purity≥97%
  • MDL No.MFCD00102573

*For research and further manufacturing use only, not for direct human use.

2,3,4-Trifluorobenzenesulfonyl chloride|CS-0132312

Structure of 175278-08-7

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General Information

  • CAS No. 175278-08-7
  • Cat. No. CS-0132312
  • Purity ≥97%
  • MDL No. MFCD00102573
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₆H₂ClF₃O₂S
  • Molecular Weight 230.59
  • Synonym(s) Benzenesulfonyl chloride, 2,3,4-trifluoro- (9CI)
  • SMILES O=S(C1=CC=C(F)C(F)=C1F)(Cl)=O

Description

2,3,4-Trifluorobenzenesulfonyl chloride features a trifluorinated aromatic ring that enhances electrophilicity and stability. This sulfonyl chloride derivative enables efficient sulfonation of nucleophiles under mild conditions, offering high reactivity with amines and alcohols. The electron-withdrawing fluorine atoms stabilize the sulfonyl group while improving solubility in organic media.

Application

2,3,4-Trifluorobenzenesulfonyl chloride serves as a highly effective sulfonylating agent for the synthesis of trifluoromethyl-substituted sulfonamides and sulfonates. Its enhanced electrophilicity due to the electron-withdrawing trifluoromethyl group enables efficient reaction with amines and alcohols under mild conditions. The reagent exhibits good bench stability and facilitates clean, high-yielding transformations with broad functional group tolerance, making it a practical choice for constructing fluorinated building blocks in medicinal chemistry and materials science applications.

Safety Information

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GHS Pictogram :
GHS No : GHS05
Signal Word : Danger
UN#: 3265
Class : 8
Packing Group : Ⅱ
Hazard Statements : H314
Precautionary Statements : P260-P264-P280-P301+P330+P331-P304+P340-P363-P405-P501

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Computational Chemistry Data

  • TPSA   34.14
  • LogP   2.0314
  • H_Acceptors   2
  • H_Donors   0
  • Rotatable_Bonds   1

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