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Atomfair 4-Bromo-3,5-difluorophenol C6H3BrF2O

Description 4-Bromo-3,5-difluorophenol (CAS No. 130191-91-2) is a high-purity halogenated phenol derivative with the molecular formula C6H3BrF2O . This specialized organic compound features a phenolic core substituted with bromine and two fluorine atoms at the 4, 3, and 5 positions, respectively, making it a valuable intermediate for advanced synthetic applications. Its precise molecular weight (209.99 g/mol) and structural rigidity ensure consistent reactivity in electrophilic aromatic substitutions and cross-coupling reactions. Ideal for pharmaceutical, agrochemical, and materials science research, this compound is supplied in sealed packaging under inert conditions to guarantee stability and purity (>97% by HPLC). Handle with care in a controlled…

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Description

Description

4-Bromo-3,5-difluorophenol (CAS No. 130191-91-2) is a high-purity halogenated phenol derivative with the molecular formula C6H3BrF2O. This specialized organic compound features a phenolic core substituted with bromine and two fluorine atoms at the 4, 3, and 5 positions, respectively, making it a valuable intermediate for advanced synthetic applications. Its precise molecular weight (209.99 g/mol) and structural rigidity ensure consistent reactivity in electrophilic aromatic substitutions and cross-coupling reactions. Ideal for pharmaceutical, agrochemical, and materials science research, this compound is supplied in sealed packaging under inert conditions to guarantee stability and purity (>97% by HPLC). Handle with care in a controlled environment due to its potential sensitivity to light and moisture.

  • CAS No: 130191-91-2
  • Molecular Formula: C6H3BrF2O
  • Molecular Weight: 208.99
  • Exact Mass: 207.93353
  • Monoisotopic Mass: 207.93353
  • IUPAC Name: 4-bromo-3,5-difluorophenol
  • SMILES: C1=C(C=C(C(=C1F)Br)F)O
  • Synonyms: 4-Bromo-3,5-difluorophenol, 130191-91-2, DTXSID40428269, DTXCID60379103, 642-656-6

Application

4-Bromo-3,5-difluorophenol serves as a key building block in the synthesis of fluorinated aromatic compounds, particularly in pharmaceutical candidates targeting CNS disorders. Its electron-withdrawing substituents enhance reactivity in Suzuki-Miyaura and Buchwald-Hartwig couplings for drug discovery. The compound is also utilized in agrochemical research to develop novel herbicides with improved metabolic stability. Additionally, it finds niche applications in materials science for designing liquid crystals and flame retardants.

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