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CS-W001157 4
Total: USD 88.00

2-Fluoro-4-nitrobenzene-1-sulfonyl chloride

  • CAS No. 1146290-36-9

  • Cat. No. CS-0157164
  • Purity≥97%
  • MDL No.MFCD11858095

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

2-Fluoro-4-nitrobenzene-1-sulfonyl chloride|CS-0157164

Structure of 1146290-36-9

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General Information

  • CAS No. 1146290-36-9
  • Cat. No. CS-0157164
  • Purity ≥97%
  • MDL No. MFCD11858095
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₆H₃ClFNO₄S
  • Molecular Weight 239.61
  • Synonym(s) None
  • SMILES C1=CC(=C(C=C1[N+](=O)[O-])F)S(=O)(=O)Cl

Description

2-Fluoro-4-nitrobenzene-1-sulfonyl chloride features a fluorine atom at the ortho position and a nitro group at the para position relative to the sulfonyl chloride, creating an electron-deficient aryl system. This combination enhances reactivity in nucleophilic aromatic substitution processes. The sulfonyl chloride moiety enables efficient coupling with amines and alcohols under mild conditions, facilitating the synthesis of sulfonamide and sulfonate derivatives. The molecule exhibits good bench stability and moisture tolerance, simplifying handling in synthetic workflows.

Application

2-Fluoro-4-nitrobenzene-1-sulfonyl chloride serves as a versatile sulfonylating agent for the synthesis of sulfonamide derivatives, enabling efficient functionalization of amines under mild conditions. Its electron-withdrawing nitro and fluorine substituents enhance reactivity while maintaining bench stability, facilitating clean reactions with broad functional group tolerance. The compound is particularly valuable in constructing heterocyclic scaffolds and bioactive intermediates common in medicinal chemistry workflows.

Safety Information

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GHS Pictogram :
GHS No : GHS05
Signal Word : Danger
UN#: 3261
Class : 8
Packing Group : Ⅲ
Hazard Statements : H302-H314
Precautionary Statements : P260-P264-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P363-P405-P501

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Computational Chemistry Data

  • TPSA   77.28
  • LogP   1.6614
  • H_Acceptors   4
  • H_Donors   0
  • Rotatable_Bonds   2

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