Cas no 1806983-87-8 (2,4-Bis(trifluoromethyl)-5-bromobenzenesulfonyl chloride)

2,4-Bis(trifluoromethyl)-5-bromobenzenesulfonyl chloride is a highly reactive sulfonyl chloride derivative, primarily used as a versatile intermediate in organic synthesis and pharmaceutical applications. Its key structural features include two electron-withdrawing trifluoromethyl groups and a bromine substituent, which enhance its reactivity in nucleophilic substitution and cross-coupling reactions. The sulfonyl chloride moiety facilitates the introduction of sulfonamide or sulfonate functionalities, making it valuable for constructing complex molecules. Its stability under controlled conditions and compatibility with a range of reagents underscore its utility in fine chemical synthesis. This compound is particularly suited for applications requiring selective functionalization in trifluoromethyl-substituted aromatic systems.
2,4-Bis(trifluoromethyl)-5-bromobenzenesulfonyl chloride structure
1806983-87-8 structure
Product Name:2,4-Bis(trifluoromethyl)-5-bromobenzenesulfonyl chloride
CAS No:1806983-87-8
MF:C8H2BrClF6O2S
MW:391.512700557709
CID:4971097
Update Time:2025-10-15

2,4-Bis(trifluoromethyl)-5-bromobenzenesulfonyl chloride Chemical and Physical Properties

Names and Identifiers

    • 2,4-Bis(trifluoromethyl)-5-bromobenzenesulfonyl chloride
    • Inchi: 1S/C8H2BrClF6O2S/c9-5-2-6(19(10,17)18)4(8(14,15)16)1-3(5)7(11,12)13/h1-2H
    • InChI Key: SVXVCOODSDQYOQ-UHFFFAOYSA-N
    • SMILES: BrC1=CC(=C(C(F)(F)F)C=C1C(F)(F)F)S(=O)(=O)Cl

Computed Properties

  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 8
  • Heavy Atom Count: 19
  • Rotatable Bond Count: 1
  • Complexity: 428
  • XLogP3: 4.4
  • Topological Polar Surface Area: 42.5

2,4-Bis(trifluoromethyl)-5-bromobenzenesulfonyl chloride Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
Alichem
A013024913-1g
2,4-Bis(trifluoromethyl)-5-bromobenzenesulfonyl chloride
1806983-87-8 97%
1g
1,490.00 USD 2021-06-24

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