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Atomfair Quinoline-3-boronic acid C9H8BNO2

Description Quinoline-3-boronic Acid (CAS No. 191162-39-7) is a high-purity boronic acid derivative with the molecular formula C9H8BNO2. This compound, also known as quinolin-3-ylboronic acid , is a versatile building block in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. Its quinoline backbone provides a rigid aromatic structure, making it valuable for constructing complex heterocyclic systems in pharmaceuticals, agrochemicals, and materials science. Our product is rigorously tested for purity (typically ??95% by HPLC) and is supplied as a white to off-white crystalline powder. It is stable under inert conditions but should be stored in a cool, dry place to prevent degradation. Suitable…

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Description

Description

Quinoline-3-boronic Acid (CAS No. 191162-39-7) is a high-purity boronic acid derivative with the molecular formula C9H8BNO2. This compound, also known as quinolin-3-ylboronic acid, is a versatile building block in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. Its quinoline backbone provides a rigid aromatic structure, making it valuable for constructing complex heterocyclic systems in pharmaceuticals, agrochemicals, and materials science. Our product is rigorously tested for purity (typically ??95% by HPLC) and is supplied as a white to off-white crystalline powder. It is stable under inert conditions but should be stored in a cool, dry place to prevent degradation. Suitable for use in medicinal chemistry, catalysis, and polymer research, this reagent is packaged under nitrogen to ensure long-term stability.

  • CAS No: 191162-39-7
  • Molecular Formula: C9H8BNO2
  • Molecular Weight: 172.98
  • Exact Mass: 173.0648087
  • Monoisotopic Mass: 173.0648087
  • IUPAC Name: quinolin-3-ylboronic acid
  • SMILES: B(C1=CC2=CC=CC=C2N=C1)(O)O
  • Synonyms: Quinoline-3-boronic Acid, 640-162-5, 3-quinolineboronic acid, 191162-39-7, Quinolin-3-ylboronic Acid

Application

Quinoline-3-boronic Acid is widely used in palladium-catalyzed cross-coupling reactions to form biaryl or heteroaryl linkages, key steps in drug discovery. It serves as a precursor for fluorescent probes and metal-organic frameworks (MOFs) due to its conjugated quinoline core. Researchers also employ it in the synthesis of kinase inhibitors and other bioactive molecules targeting cancer and inflammation.

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