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CS-W001157 4
Total: USD 88.00

2,6-Difluorobenzene-1-sulfonyl chloride

  • CAS No. 60230-36-6

  • Cat. No. CS-W007930
  • Purity≥98%
  • MDL No.MFCD00085004

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

2,6-Difluorobenzene-1-sulfonyl chloride|CS-W007930

Structure of 60230-36-6

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General Information

  • CAS No. 60230-36-6
  • Cat. No. CS-W007930
  • Purity ≥98%
  • MDL No. MFCD00085004
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₆H₃ClF₂O₂S
  • Molecular Weight 212.60
  • Synonym(s) 2,6-Difluorobenzenesulfonyl chloride
  • SMILES O=S(C1=C(F)C=CC=C1F)(Cl)=O

Description

2,6-Difluorobenzene-1-sulfonyl chloride features a sulfonyl chloride group flanked by two fluorine atoms at the 2 and 6 positions, enhancing electrophilicity and directing substitution. This electron-deficient arylsulfonyl chloride enables selective coupling in synthetic routes requiring high reactivity under mild conditions.

Application

2,6-Difluorobenzene-1-sulfonyl chloride serves as a versatile sulfonylating agent for the selective introduction of sulfonamide groups under mild conditions. Its ortho-fluoro substitution enhances electrophilicity while maintaining bench stability and compatibility with diverse functional groups. The reagent facilitates efficient synthesis of sulfonamide-containing building blocks used in medicinal chemistry and agrochemical development, offering predictable reactivity and straightforward purification via crystallization or chromatography.

Synthesis

  • Route1
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      372-18-9
    • ~%
    • In-stock
      2,6-Difluorobenzene-1-sulfonyl chloride|CS-W007930
      60230-36-6

    References

    • US2013/53562 A1, ; Paragraph 0073 ;

Safety Information

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

Quality Control

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Computational Chemistry Data

  • TPSA   34.14
  • LogP   1.8923
  • H_Acceptors   2
  • H_Donors   0
  • Rotatable_Bonds   1

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