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Atomfair 2-Bromo-6-fluorophenol C6H4BrFO

Description 2-Bromo-6-fluorophenol (CAS No. 2040-89-3) is a high-purity halogenated phenol derivative with the molecular formula C6H4BrFO . This compound is a valuable building block in organic synthesis, particularly in pharmaceutical and agrochemical research. Its unique structure, featuring both bromine and fluorine substituents on the phenolic ring, enables versatile reactivity in cross-coupling reactions, nucleophilic substitutions, and as a precursor for advanced intermediates. Available in >98% purity (GC), this product is rigorously tested for consistency and suitability in sensitive applications. Packaged under inert gas to ensure stability, it is ideal for researchers requiring precise control over reaction conditions. Store in a cool,…

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Description

Description

2-Bromo-6-fluorophenol (CAS No. 2040-89-3) is a high-purity halogenated phenol derivative with the molecular formula C6H4BrFO. This compound is a valuable building block in organic synthesis, particularly in pharmaceutical and agrochemical research. Its unique structure, featuring both bromine and fluorine substituents on the phenolic ring, enables versatile reactivity in cross-coupling reactions, nucleophilic substitutions, and as a precursor for advanced intermediates. Available in >98% purity (GC), this product is rigorously tested for consistency and suitability in sensitive applications. Packaged under inert gas to ensure stability, it is ideal for researchers requiring precise control over reaction conditions. Store in a cool, dry place away from light to maintain optimal quality.

  • CAS No: 2040-89-3
  • Molecular Formula: C6H4BrFO
  • Molecular Weight: 191.00
  • Exact Mass: 189.94296
  • Monoisotopic Mass: 189.94296
  • IUPAC Name: 2-bromo-6-fluorophenol
  • SMILES: C1=CC(=C(C(=C1)Br)O)F
  • Synonyms: 2-BROMO-6-FLUOROPHENOL, 2040-89-3, DTXSID00381366, DTXCID80332391, 807-795-0

Application

2-Bromo-6-fluorophenol serves as a key intermediate in the synthesis of bioactive molecules, including potential drug candidates and specialty chemicals. Its halogenated aromatic structure is utilized in Suzuki-Miyaura and Buchwald-Hartwig coupling reactions to construct complex scaffolds. Researchers also employ it in the development of fluorinated liquid crystals and materials science applications. The compound’s reactivity makes it suitable for modifying phenolic cores in medicinal chemistry programs.

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