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Atomfair 2,4-Dibromo-1-fluorobenzene C6H3Br2F

Description 2,4-Dibromo-1-fluorobenzene (CAS No. 1435-53-6) is a high-purity halogenated aromatic compound with the molecular formula C6H3Br2F . This organofluorine building block features two bromine substituents at the 2- and 4-positions and a fluorine at the 1-position of the benzene ring, offering unique reactivity for electrophilic aromatic substitution and metal-catalyzed coupling reactions. Provided as a crystalline solid with ??98% purity (GC), it is ideal for pharmaceutical intermediates, agrochemical synthesis, and materials science research. Packaged under inert gas in amber glass vials to ensure stability, this compound is characterized by1H/13C NMR, GC-MS, and elemental analysis. Handle with appropriate PPE in well-ventilated areas…

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Description

Description

2,4-Dibromo-1-fluorobenzene (CAS No. 1435-53-6) is a high-purity halogenated aromatic compound with the molecular formula C6H3Br2F. This organofluorine building block features two bromine substituents at the 2- and 4-positions and a fluorine at the 1-position of the benzene ring, offering unique reactivity for electrophilic aromatic substitution and metal-catalyzed coupling reactions. Provided as a crystalline solid with ??98% purity (GC), it is ideal for pharmaceutical intermediates, agrochemical synthesis, and materials science research. Packaged under inert gas in amber glass vials to ensure stability, this compound is characterized by 1H/13C NMR, GC-MS, and elemental analysis. Handle with appropriate PPE in well-ventilated areas due to halogenated compound hazards.

  • CAS No: 1435-53-6
  • Molecular Formula: C6H3Br2F
  • Molecular Weight: 253.89
  • Exact Mass: 253.85650
  • Monoisotopic Mass: 251.85855
  • IUPAC Name: 2,4-dibromo-1-fluorobenzene
  • SMILES: C1=CC(=C(C=C1Br)Br)F
  • Synonyms: 2,4-Dibromo-1-fluorobenzene, 1435-53-6, EINECS 215-860-4, DTXSID70162447, NSC 88308

Application

2,4-Dibromo-1-fluorobenzene serves as a versatile precursor in Suzuki-Miyaura and Ullmann coupling reactions to synthesize biaryl compounds for liquid crystal materials. Its electron-deficient aromatic ring facilitates nucleophilic substitution in pharmaceutical intermediates, particularly for fluorinated drug candidates. Researchers also employ it as a scaffold for developing flame retardants and halogenated organic semiconductors.

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