Description

4-Bromo-1,2-dichloro-1,1,2-trifluorobutane (CAS No. 234096-23-2) is a high-purity halogenated organic compound with the molecular formula C₄H₄BrCl₂F₃. This specialty chemical is designed for advanced research and industrial applications, offering exceptional reactivity due to its unique combination of bromine, chlorine, and fluorine substituents. Its IUPAC name, 4-bromo-1,2-dichloro-1,1,2-trifluorobutane, reflects its precise structural configuration, ensuring accurate identification for synthetic and analytical purposes. Available in rigorously controlled batches, this compound is ideal for organofluorine chemistry, pharmaceutical intermediates, and material science research. Each shipment includes comprehensive analytical data (GC/MS, NMR) to guarantee consistency and purity for your critical experiments.

Properties

• CAS Number: 234096-23-2
• Complexity: 121
• IUPAC Name: 4-bromo-1,2-dichloro-1,1,2-trifluoro-butane
• InChI: InChI=1S/C4H4BrCl2F3/c5-2-1-3(6,8)4(7,9)10/h1-2H2
• InChI Key: ZKLSXROKZJZFCB-UHFFFAOYSA-N
• Exact Mass: 257.88255
• Molecular Formula: C4H4BrCl2F3
• Molecular Weight: 259.88
• SMILES: C(CBr)C(C(F)(F)Cl)(F)Cl
• Monoisotopic Mass: 257.88255
• Synonyms: 4-bromo-1,2-dichloro-1,1,2-trifluorobutane, 234096-23-2, MFCD00792408, 1-Bromo-3,4-dichloro-3,4,4-trifluorobutane, ZKLSXROKZJZFCB-UHFFFAOYSA-N, SBB102240, AKOS025211690, EN300-7654326

Application

4-Bromo-1,2-dichloro-1,1,2-trifluorobutane serves as a versatile building block in fluorinated compound synthesis, particularly for pharmaceutical candidates requiring selective halogenation. Its multi-halogenated structure enables participation in nucleophilic substitution and cross-coupling reactions for agrochemical development. Researchers utilize this compound in polymer modification studies to introduce flame-retardant or hydrophobic properties. The bromine moiety allows further functionalization via Suzuki or Grignard reactions in complex molecule construction.

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