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Atomfair 4-Bromo-2-fluorobenzenesulphonamide C6H5BrFNO2S

Description 4-Bromo-2-fluorobenzenesulphonamide (CAS No. 214210-30-7) is a high-purity sulfonamide derivative with the molecular formula C6H5BrFNO2S . This compound features a bromo-fluorinated benzene ring coupled with a sulfonamide functional group, making it a valuable intermediate in organic synthesis and pharmaceutical research. Its IUPAC name, 4-bromo-2-fluorobenzenesulfonamide , reflects its precise structural configuration. Ideal for researchers, this product is rigorously tested for purity and stability, ensuring reliable performance in advanced chemical applications. Available in various quantities, it is packaged under controlled conditions to maintain integrity.

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Description

Description

4-Bromo-2-fluorobenzenesulphonamide (CAS No. 214210-30-7) is a high-purity sulfonamide derivative with the molecular formula C6H5BrFNO2S. This compound features a bromo-fluorinated benzene ring coupled with a sulfonamide functional group, making it a valuable intermediate in organic synthesis and pharmaceutical research. Its IUPAC name, 4-bromo-2-fluorobenzenesulfonamide, reflects its precise structural configuration. Ideal for researchers, this product is rigorously tested for purity and stability, ensuring reliable performance in advanced chemical applications. Available in various quantities, it is packaged under controlled conditions to maintain integrity.

  • CAS No: 214210-30-7
  • Molecular Formula: C6H5BrFNO2S
  • Molecular Weight: 254.08
  • Exact Mass: 252.92084
  • Monoisotopic Mass: 252.92084
  • IUPAC Name: 4-bromo-2-fluorobenzenesulfonamide
  • SMILES: C1=CC(=C(C=C1Br)F)S(=O)(=O)N
  • Synonyms: 4-bromo-2-fluorobenzenesulphonamide, 674-851-7, 4-Bromo-2-fluorobenzenesulfonamide, 214210-30-7, 4-bromo-2-fluorobenzene-1-sulfonamide

Application

4-Bromo-2-fluorobenzenesulphonamide is widely used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of sulfonamide-based drugs. Its unique halogenated structure makes it suitable for cross-coupling reactions in medicinal chemistry. Researchers also employ it in the study of enzyme inhibition and receptor binding due to its sulfonamide moiety. Additionally, it serves as a building block for agrochemicals and specialty chemicals requiring bromo-fluorinated aromatic systems.

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