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Atomfair 3,5-Difluorobenzyl alcohol C7H6F2O

Description 3,5-Difluorobenzyl alcohol (CAS No. 79538-20-8) is a high-purity fluorinated benzyl alcohol derivative with the molecular formula C7H6F2O . This compound, also known by its IUPAC name (3,5-difluorophenyl)methanol , is a valuable building block in pharmaceutical, agrochemical, and materials science research. Its unique structure, featuring two fluorine atoms at the meta positions of the benzyl ring, enhances its reactivity and utility in nucleophilic substitutions and cross-coupling reactions. Our product is rigorously tested to ensure ??98% purity (GC) and is supplied in sealed containers under inert atmosphere to maintain stability. Ideal for use in Suzuki-Miyaura couplings, etherifications, and as a precursor…

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Description

Description

3,5-Difluorobenzyl alcohol (CAS No. 79538-20-8) is a high-purity fluorinated benzyl alcohol derivative with the molecular formula C7H6F2O. This compound, also known by its IUPAC name (3,5-difluorophenyl)methanol, is a valuable building block in pharmaceutical, agrochemical, and materials science research. Its unique structure, featuring two fluorine atoms at the meta positions of the benzyl ring, enhances its reactivity and utility in nucleophilic substitutions and cross-coupling reactions.

Our product is rigorously tested to ensure ??98% purity (GC) and is supplied in sealed containers under inert atmosphere to maintain stability. Ideal for use in Suzuki-Miyaura couplings, etherifications, and as a precursor for advanced intermediates, this reagent is a must-have for synthetic chemists working on fluorinated compounds.

Key identifiers: DTXSID40335045, DTXCID90286134, EC 632-822-6.

  • CAS No: 79538-20-8
  • Molecular Formula: C7H6F2O
  • Molecular Weight: 144.12
  • Exact Mass: 144.03867113
  • Monoisotopic Mass: 144.03867113
  • IUPAC Name: (3,5-difluorophenyl)methanol
  • SMILES: C1=C(C=C(C=C1F)F)CO
  • Synonyms: 3,5-Difluorobenzyl alcohol, 79538-20-8, DTXSID40335045, DTXCID90286134, 632-822-6

Application

3,5-Difluorobenzyl alcohol serves as a versatile intermediate in the synthesis of fluorinated pharmaceuticals, including kinase inhibitors and CNS-active compounds. Its benzyl alcohol group enables easy conversion to halides or ethers, while the difluoro substitution pattern enhances metabolic stability in drug candidates. Researchers also utilize it to prepare liquid crystals and specialty polymers with tailored dielectric properties.

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