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Atomfair (4-Butoxy-2,3-difluorophenyl)boronic acid C10H13BF2O3

Description (4-Butoxy-2,3-difluorophenyl)boronic acid (CAS No. 156487-12-6) is a high-purity boronic acid derivative with the molecular formula C10H13BF2O3. This compound features a butoxy-substituted difluorophenyl ring coupled with a reactive boronic acid functional group, making it a versatile intermediate in organic synthesis and pharmaceutical research. Its unique structure enables selective cross-coupling reactions, such as Suzuki-Miyaura couplings, for the construction of complex biaryl systems. The product is supplied as a fine white to off-white crystalline powder with ??95% purity (HPLC), ensuring optimal performance in sensitive applications. Store in a cool, dry place under inert atmosphere to maintain stability and prevent degradation.

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Description

Description

(4-Butoxy-2,3-difluorophenyl)boronic acid (CAS No. 156487-12-6) is a high-purity boronic acid derivative with the molecular formula C10H13BF2O3. This compound features a butoxy-substituted difluorophenyl ring coupled with a reactive boronic acid functional group, making it a versatile intermediate in organic synthesis and pharmaceutical research. Its unique structure enables selective cross-coupling reactions, such as Suzuki-Miyaura couplings, for the construction of complex biaryl systems. The product is supplied as a fine white to off-white crystalline powder with ??95% purity (HPLC), ensuring optimal performance in sensitive applications. Store in a cool, dry place under inert atmosphere to maintain stability and prevent degradation.

  • CAS No: 156487-12-6
  • Molecular Formula: C10H13BF2O3
  • Molecular Weight: 230.02
  • Exact Mass: 230.0925808
  • Monoisotopic Mass: 230.0925808
  • IUPAC Name: (4-butoxy-2,3-difluorophenyl)boronic acid
  • SMILES: B(C1=C(C(=C(C=C1)OCCCC)F)F)(O)O
  • Synonyms: 156487-12-6, (4-Butoxy-2,3-difluorophenyl)boronic acid, DTXSID10709239, DTXCID10659987, 692-793-0

Application

(4-Butoxy-2,3-difluorophenyl)boronic acid is widely used as a key building block in medicinal chemistry for the synthesis of fluorinated drug candidates. It serves as a critical intermediate in Suzuki-Miyaura cross-coupling reactions to create biaryl structures prevalent in agrochemicals and OLED materials. Researchers also employ it in the development of boron-based sensors and covalent organic frameworks (COFs) due to its balanced reactivity and steric profile.

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