Atomfair 4-Fluorophenylboronic acid 4-FPBA C6H6BFO2

Description 4-Fluorophenylboronic Acid (CAS No. 1765-93-1) is a high-purity boronic acid derivative with the molecular formula C6H6BFO2, widely utilized in organic synthesis and pharmaceutical research. This compound, also known as (4-fluorophenyl)boronic acid , features a fluorinated phenyl group attached to a boronic acid moiety, making it a versatile building block for Suzuki-Miyaura cross-coupling reactions. Its high reactivity and stability under various conditions ensure excellent yields in the formation of carbon-carbon bonds. Ideal for researchers and scientists, our product is rigorously tested for purity (typically ??97% by HPLC) and is supplied as a white to off-white crystalline powder. Store in a…

Description

Description

4-Fluorophenylboronic Acid (CAS No. 1765-93-1) is a high-purity boronic acid derivative with the molecular formula C6H6BFO2, widely utilized in organic synthesis and pharmaceutical research. This compound, also known as (4-fluorophenyl)boronic acid, features a fluorinated phenyl group attached to a boronic acid moiety, making it a versatile building block for Suzuki-Miyaura cross-coupling reactions. Its high reactivity and stability under various conditions ensure excellent yields in the formation of carbon-carbon bonds. Ideal for researchers and scientists, our product is rigorously tested for purity (typically ??97% by HPLC) and is supplied as a white to off-white crystalline powder. Store in a cool, dry place under inert conditions to maintain optimal stability.

  • CAS No: 1765-93-1
  • Molecular Formula: C6H6BFO2
  • Molecular Weight: 139.92
  • Exact Mass: 140.0444878
  • Monoisotopic Mass: 140.0444878
  • IUPAC Name: (4-fluorophenyl)boronic acid
  • SMILES: B(C1=CC=C(C=C1)F)(O)O
  • Synonyms: 4-Fluorophenylboronic acid, 1765-93-1, (4-fluorophenyl)boronic acid, p-fluorophenylboronic acid, BORONIC ACID, B-(4-FLUOROPHENYL)-

Application

4-Fluorophenylboronic acid is extensively used in pharmaceutical intermediates and agrochemical synthesis due to its role in Suzuki-Miyaura cross-coupling reactions. It serves as a key precursor in the development of fluorinated aromatic compounds, which are critical in drug discovery and material science. Researchers also employ it in the synthesis of sensors and organic electronic materials owing to its stable boronic acid functionality.

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