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Atomfair Bis(4-methylphenyl)borinic acid C14H15BO

Description Bis(4-methylphenyl)borinic acid (CAS No. 66117-64-4) is an organoboron compound with the molecular formula C14H15BO . This high-purity reagent is widely used in organic synthesis, catalysis, and materials science due to its unique boron-centered Lewis acidity and stability. The compound features two para-methylphenyl groups attached to a borinic acid moiety, making it a versatile intermediate for cross-coupling reactions, polymerization catalysts, and ligand design. Available in crystalline or powder form, our product is rigorously tested for purity (typically ??95% by HPLC or NMR) and is packaged under inert conditions to ensure long-term stability. Ideal for researchers developing novel boron-containing polymers, pharmaceuticals,…

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Description

Description

Bis(4-methylphenyl)borinic acid (CAS No. 66117-64-4) is an organoboron compound with the molecular formula C14H15BO. This high-purity reagent is widely used in organic synthesis, catalysis, and materials science due to its unique boron-centered Lewis acidity and stability. The compound features two para-methylphenyl groups attached to a borinic acid moiety, making it a versatile intermediate for cross-coupling reactions, polymerization catalysts, and ligand design. Available in crystalline or powder form, our product is rigorously tested for purity (typically ??95% by HPLC or NMR) and is packaged under inert conditions to ensure long-term stability. Ideal for researchers developing novel boron-containing polymers, pharmaceuticals, or optoelectronic materials.

  • CAS No: 66117-64-4
  • Molecular Formula: C14H15BO
  • Molecular Weight: 210.08
  • Exact Mass: 210.1215953
  • Monoisotopic Mass: 210.1215953
  • IUPAC Name: bis(4-methylphenyl)borinic acid
  • SMILES: B(C1=CC=C(C=C1)C)(C2=CC=C(C=C2)C)O
  • Synonyms: 66117-64-4, bis(4-methylphenyl)borinic acid, DTXSID30521677, DTXCID80472483, Hydroxydip-tolylborane

Application

Bis(4-methylphenyl)borinic acid serves as a key precursor in Suzuki-Miyaura cross-coupling reactions for biaryl synthesis. Its Lewis acidic properties make it valuable in catalytic systems for polymerization and C-X bond activation. Researchers utilize this compound to develop boron-doped organic semiconductors and as a building block for luminescent materials.

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