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CS-W001157 4
Total: USD 88.00

3,4,5-Trifluorobenzenesulfonyl chloride

  • CAS No. 351003-43-5

  • Cat. No. CS-0127976
  • Purity≥96%
  • MDL No.None

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

3,4,5-Trifluorobenzenesulfonyl chloride|CS-0127976

Structure of 351003-43-5

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General Information

  • CAS No. 351003-43-5
  • Cat. No. CS-0127976
  • Purity ≥96%
  • MDL No. None
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₆H₂ClF₃O₂S
  • Molecular Weight 230.59
  • Synonym(s) 3,4,5-Trifluorobenzenesulphonyl chloride
  • SMILES O=S(C1=CC(F)=C(C(F)=C1)F)(Cl)=O

Description

3,4,5-Trifluorobenzenesulfonyl chloride features a highly electron-deficient aromatic ring that enhances reactivity in sulfonylation processes. This bench-stable reagent facilitates efficient introduction of sulfonate groups into nucleophilic substrates under mild conditions, offering superior selectivity and yield in synthetic applications.

Application

3,4,5-Trifluorobenzenesulfonyl chloride serves as a highly reactive sulfonylating agent for the efficient introduction of trifluoromethyl-substituted sulfonamide groups. Its electron-deficient aromatic ring enhances electrophilicity, enabling rapid reaction with amines and alcohols under mild conditions. The compound exhibits excellent bench stability and facilitates clean, high-yielding transformations, making it ideal for constructing fluorinated sulfonamide building blocks in medicinal chemistry and agrochemical synthesis.

Safety Information

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GHS Pictogram :
GHS No : GHS02,GHS05
Signal Word : Danger
UN#: 2924
Class : 3,8
Packing Group : Ⅲ
Hazard Statements : H225-H314
Precautionary Statements : P210-P240-P241-P280-P370+P378

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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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