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Atomfair Phenylethane Boronic Acid C8H11BO2

Description Phenylethane Boronic Acid (CAS No. 34420-17-2) is a high-purity boronic acid derivative with the molecular formula C8H11BO2and IUPAC name 2-phenylethylboronic acid . This organoboron compound is widely utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, due to its excellent reactivity and stability. Our product is rigorously tested to ensure ??95% purity (HPLC/GC) and is supplied as a white to off-white crystalline powder, packaged under inert conditions to prevent degradation. Ideal for pharmaceutical intermediates, materials science, and catalysis research, this compound is characterized by NMR, FTIR, and mass spectrometry for quality assurance. Store in a cool, dry place away…

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Description

Description

Phenylethane Boronic Acid (CAS No. 34420-17-2) is a high-purity boronic acid derivative with the molecular formula C8H11BO2 and IUPAC name 2-phenylethylboronic acid. This organoboron compound is widely utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, due to its excellent reactivity and stability. Our product is rigorously tested to ensure ??95% purity (HPLC/GC) and is supplied as a white to off-white crystalline powder, packaged under inert conditions to prevent degradation. Ideal for pharmaceutical intermediates, materials science, and catalysis research, this compound is characterized by NMR, FTIR, and mass spectrometry for quality assurance. Store in a cool, dry place away from moisture and oxidizing agents.

  • CAS No: 34420-17-2
  • Molecular Formula: C8H11BO2
  • Molecular Weight: 149.98
  • Exact Mass: 150.0852098
  • Monoisotopic Mass: 150.0852098
  • IUPAC Name: 2-phenylethylboronic acid
  • SMILES: B(CCC1=CC=CC=C1)(O)O
  • Synonyms: 34420-17-2, Phenylethane boronic acid, (2-phenylethyl)boronic acid, Boronic acid, (2-phenylethyl)-, DTXSID10188000

Application

Phenylethane Boronic Acid serves as a key intermediate in Suzuki-Miyaura cross-coupling reactions for constructing biaryl compounds in pharmaceutical and agrochemical research. It is also employed in the synthesis of boron-containing polymers and advanced materials. Researchers leverage its boronic acid functionality for sensor development and carbohydrate recognition studies.

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