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Atomfair 2-Fluoropyridine-4-boronic acid C5H5BFNO2

Description 2-Fluoropyridine-4-boronic acid (CAS No. 401815-98-3) is a high-purity boronic acid derivative with the molecular formula C5H5BFNO2and IUPAC name (2-fluoropyridin-4-yl)boronic acid . This compound is a valuable building block in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, due to its reactive boronic acid functional group and fluorinated pyridine backbone. It is supplied as a white to off-white crystalline powder with ??95% purity (HPLC), ensuring optimal performance in research and industrial applications. Suitable for use in pharmaceutical, agrochemical, and materials science research, this reagent is rigorously tested for quality, stability, and consistency. Store under inert conditions at 2-8??C to maintain stability.

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Description

Description

2-Fluoropyridine-4-boronic acid (CAS No. 401815-98-3) is a high-purity boronic acid derivative with the molecular formula C5H5BFNO2 and IUPAC name (2-fluoropyridin-4-yl)boronic acid. This compound is a valuable building block in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, due to its reactive boronic acid functional group and fluorinated pyridine backbone. It is supplied as a white to off-white crystalline powder with ??95% purity (HPLC), ensuring optimal performance in research and industrial applications. Suitable for use in pharmaceutical, agrochemical, and materials science research, this reagent is rigorously tested for quality, stability, and consistency. Store under inert conditions at 2-8??C to maintain stability.

  • CAS No: 401815-98-3
  • Molecular Formula: C5H5BFNO2
  • Molecular Weight: 140.91
  • Exact Mass: 141.0397367
  • Monoisotopic Mass: 141.0397367
  • IUPAC Name: (2-fluoropyridin-4-yl)boronic acid
  • SMILES: B(C1=CC(=NC=C1)F)(O)O
  • Synonyms: 2-Fluoropyridine-4-boronic acid, 401815-98-3, DTXSID40382635, DTXCID20333660, 640-138-4

Application

2-Fluoropyridine-4-boronic acid is widely used as a key intermediate in Suzuki-Miyaura cross-coupling reactions to synthesize biaryl compounds for pharmaceuticals and agrochemicals. Its fluorinated pyridine moiety enhances metabolic stability and bioavailability in drug discovery. Researchers also employ it in the development of advanced materials, such as organic electronic components and metal-organic frameworks (MOFs).

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