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Atomfair (4-Bromo-2-fluorophenyl)methanol 4-Bromo-2-fluorobenzyl alcohol C7H6BrFO

Description (4-Bromo-2-fluorophenyl)methanol (CAS No. 188582-62-9) is a high-purity aromatic alcohol derivative with the molecular formula C7H6BrFO. This compound features a bromo and fluoro substitution on the phenyl ring, making it a versatile intermediate for pharmaceutical, agrochemical, and materials science research. Its benzyl alcohol moiety enhances reactivity in nucleophilic substitutions and cross-coupling reactions, such as Suzuki-Miyaura or Buchwald-Hartwig couplings. With a molecular weight of 205.03 g/mol, it is supplied as a white to off-white crystalline solid with ??95% purity (HPLC). Ideal for synthetic organic chemists, this product is rigorously tested for consistency, stability, and low trace metal content. Store under inert…

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Description

Description

(4-Bromo-2-fluorophenyl)methanol (CAS No. 188582-62-9) is a high-purity aromatic alcohol derivative with the molecular formula C7H6BrFO. This compound features a bromo and fluoro substitution on the phenyl ring, making it a versatile intermediate for pharmaceutical, agrochemical, and materials science research. Its benzyl alcohol moiety enhances reactivity in nucleophilic substitutions and cross-coupling reactions, such as Suzuki-Miyaura or Buchwald-Hartwig couplings. With a molecular weight of 205.03 g/mol, it is supplied as a white to off-white crystalline solid with ??95% purity (HPLC). Ideal for synthetic organic chemists, this product is rigorously tested for consistency, stability, and low trace metal content. Store under inert conditions at 2-8??C to maintain integrity.

  • CAS No: 188582-62-9
  • Molecular Formula: C7H6BrFO
  • Molecular Weight: 205.02
  • Exact Mass: 203.95861
  • Monoisotopic Mass: 203.95861
  • IUPAC Name: (4-bromo-2-fluorophenyl)methanol
  • SMILES: C1=CC(=C(C=C1Br)F)CO
  • Synonyms: (4-bromo-2-fluorophenyl)methanol, 672-500-2, 4-Bromo-2-fluorobenzyl alcohol, 188582-62-9, Benzenemethanol, 4-bromo-2-fluoro-

Application

(4-Bromo-2-fluorophenyl)methanol serves as a key building block in the synthesis of bioactive molecules, including kinase inhibitors and fluorinated drug candidates. It is employed in palladium-catalyzed cross-coupling reactions to introduce functionalized aryl groups into complex scaffolds. Researchers also utilize it to develop liquid crystals and OLED materials due to its halogenated aromatic structure.

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