Atomfair (3-Phenylphenyl)boronic acid 3-Biphenylboronic acid C12H11BO2

Description (3-Phenylphenyl)boronic acid (CAS No. 139301-27-2) is a high-purity boronic acid derivative with the molecular formula C12H11BO2, widely utilized in organic synthesis and pharmaceutical research. This compound, also known as 3-Biphenylboronic acid , features a phenyl-substituted phenylboronic acid structure, making it a versatile building block for Suzuki-Miyaura cross-coupling reactions. Its boronic acid functional group enables selective bond formation with aryl halides, facilitating the synthesis of complex biaryl systems. Ideal for researchers and industrial chemists, our product is rigorously tested for consistency, ensuring optimal reactivity and yield in catalytic applications. Available in crystalline form with ??95% purity, it is packaged under…

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Description

Description

(3-Phenylphenyl)boronic acid (CAS No. 139301-27-2) is a high-purity boronic acid derivative with the molecular formula C12H11BO2, widely utilized in organic synthesis and pharmaceutical research. This compound, also known as 3-Biphenylboronic acid, features a phenyl-substituted phenylboronic acid structure, making it a versatile building block for Suzuki-Miyaura cross-coupling reactions. Its boronic acid functional group enables selective bond formation with aryl halides, facilitating the synthesis of complex biaryl systems. Ideal for researchers and industrial chemists, our product is rigorously tested for consistency, ensuring optimal reactivity and yield in catalytic applications. Available in crystalline form with ??95% purity, it is packaged under inert conditions to maintain stability and shelf life.

  • CAS No: 139301-27-2
  • Molecular Formula: C12H11BO2
  • Molecular Weight: 198.03
  • Exact Mass: 198.0852098
  • Monoisotopic Mass: 198.0852098
  • IUPAC Name: (3-phenylphenyl)boronic acid
  • SMILES: B(C1=CC(=CC=C1)C2=CC=CC=C2)(O)O
  • Synonyms: (3-phenylphenyl)boronic Acid, 671-848-2, 3-Biphenylboronic acid, 5122-95-2, Biphenyl-3-boronic acid

Application

(3-Phenylphenyl)boronic acid is a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of biaryl structures prevalent in pharmaceuticals and agrochemicals. It serves as a ligand or precursor in catalytic systems for C-C bond formation, particularly in drug discovery and material science. Researchers also employ it in the development of sensors and organic electronic materials due to its stable boronic acid moiety.

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