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Atomfair 4-Nitrophenylboronic acid C6H6BNO4

Description 4-Nitrophenylboronic acid (CAS No. 24067-17-2) is a high-purity boronic acid derivative with the molecular formula C6H6BNO4. This compound, also known by its IUPAC name (4-nitrophenyl)boronic acid , is a versatile reagent widely used in organic synthesis, pharmaceuticals, and materials science. It features a boronic acid functional group (-B(OH)2) attached to a nitrophenyl ring, making it an excellent candidate for Suzuki-Miyaura cross-coupling reactions, a cornerstone of modern synthetic chemistry. Our product is rigorously tested for purity, ensuring optimal performance in sensitive applications. Available in various quantities, it is supplied with detailed analytical certificates (CoA) including HPLC, NMR, and MS data…

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Description

Description

4-Nitrophenylboronic acid (CAS No. 24067-17-2) is a high-purity boronic acid derivative with the molecular formula C6H6BNO4. This compound, also known by its IUPAC name (4-nitrophenyl)boronic acid, is a versatile reagent widely used in organic synthesis, pharmaceuticals, and materials science. It features a boronic acid functional group (-B(OH)2) attached to a nitrophenyl ring, making it an excellent candidate for Suzuki-Miyaura cross-coupling reactions, a cornerstone of modern synthetic chemistry. Our product is rigorously tested for purity, ensuring optimal performance in sensitive applications. Available in various quantities, it is supplied with detailed analytical certificates (CoA) including HPLC, NMR, and MS data to guarantee traceability and consistency for researchers and industrial scientists.

  • CAS No: 24067-17-2
  • Molecular Formula: C6H6BNO4
  • Molecular Weight: 166.93
  • Exact Mass: 167.0389878
  • Monoisotopic Mass: 167.0389878
  • IUPAC Name: (4-nitrophenyl)boronic acid
  • SMILES: B(C1=CC=C(C=C1)[N+](=O)[O-])(O)O
  • Synonyms: 4-Nitrophenylboronic acid, 24067-17-2, DTXSID50378549, DTXCID50329576, 627-647-7

Application

4-Nitrophenylboronic acid is primarily employed as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of biaryl compounds, which are critical in pharmaceutical and agrochemical development. It also serves as a building block in the preparation of sensors and molecular recognition systems due to its boronic acid group’s affinity for diols and sugars. Additionally, this compound finds use in polymer chemistry and materials science for modifying surfaces or creating functionalized materials with tailored properties.

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