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Atomfair 2-Bromo-1-fluoro-4-methoxybenzene C7H6BrFO

Description 2-Bromo-1-fluoro-4-methoxybenzene (CAS No. 1161497-23-9) is a high-purity halogenated aromatic compound with the molecular formula C7H6BrFO . This specialty chemical features a bromo- and fluoro-substituted benzene ring with a methoxy group at the para position, making it a versatile building block for pharmaceutical, agrochemical, and materials science research. Available in >98% purity (GC), it is supplied as a clear to pale-yellow liquid with strict quality control via HPLC, NMR, and MS analysis. Ideal for Suzuki couplings, nucleophilic substitutions, and as a precursor in heterocyclic synthesis. Packaged under inert gas in amber glass vials to ensure stability. Store at 2-8??C in…

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Description

Description

2-Bromo-1-fluoro-4-methoxybenzene (CAS No. 1161497-23-9) is a high-purity halogenated aromatic compound with the molecular formula C7H6BrFO. This specialty chemical features a bromo- and fluoro-substituted benzene ring with a methoxy group at the para position, making it a versatile building block for pharmaceutical, agrochemical, and materials science research. Available in >98% purity (GC), it is supplied as a clear to pale-yellow liquid with strict quality control via HPLC, NMR, and MS analysis. Ideal for Suzuki couplings, nucleophilic substitutions, and as a precursor in heterocyclic synthesis. Packaged under inert gas in amber glass vials to ensure stability. Store at 2-8??C in a dry environment.

  • CAS No: 1161497-23-9
  • Molecular Formula: C7H6BrFO
  • Molecular Weight: 205.02
  • Exact Mass: 203.95861
  • Monoisotopic Mass: 203.95861
  • IUPAC Name: 2-bromo-1-fluoro-4-methoxybenzene
  • SMILES: COC1=CC(=C(C=C1)F)Br
  • Synonyms: 1161497-23-9, 2-Bromo-1-fluoro-4-methoxybenzene, DTXSID00590734, DTXCID50541498, 843-351-2

Application

2-Bromo-1-fluoro-4-methoxybenzene is widely used as a key intermediate in the synthesis of active pharmaceutical ingredients (APIs) and liquid crystal materials. Its unique substitution pattern enables selective functionalization in cross-coupling reactions (e.g., Buchwald-Hartwig amination). Researchers employ this compound to develop fluorinated analogs of bioactive molecules for enhanced metabolic stability. In material science, it serves as a precursor for photoactive polymers and OLED components.

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