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Atomfair (2-fluoropyridin-3-yl)boronic Acid Hydrate C5H7BFNO3

Description (2-Fluoropyridin-3-yl)boronic Acid Hydrate (CAS No. 174669-73-9) is a high-purity boronic acid derivative widely used in organic synthesis, pharmaceutical research, and material science. With the molecular formula C5H7BFNO3, this compound serves as a versatile building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in complex molecular architectures. Its hydrate form ensures stability and ease of handling under laboratory conditions. Ideal for researchers requiring precise and reliable reagents, this product is rigorously tested for quality, with NMR and HPLC validation to guarantee ??95% purity. Store in a cool, dry place under inert conditions to maintain optimal performance.

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Description

Description

(2-Fluoropyridin-3-yl)boronic Acid Hydrate (CAS No. 174669-73-9) is a high-purity boronic acid derivative widely used in organic synthesis, pharmaceutical research, and material science. With the molecular formula C5H7BFNO3, this compound serves as a versatile building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in complex molecular architectures. Its hydrate form ensures stability and ease of handling under laboratory conditions. Ideal for researchers requiring precise and reliable reagents, this product is rigorously tested for quality, with NMR and HPLC validation to guarantee ??95% purity. Store in a cool, dry place under inert conditions to maintain optimal performance.

  • CAS No: 174669-73-9
  • Molecular Formula: C5H7BFNO3
  • Molecular Weight: 158.93
  • Exact Mass: 159.0503014
  • Monoisotopic Mass: 159.0503014
  • IUPAC Name: (2-fluoropyridin-3-yl)boronic acid;hydrate
  • SMILES: B(C1=C(N=CC=C1)F)(O)O.O
  • Synonyms: (2-fluoropyridin-3-yl)boronic Acid Hydrate, 1264133-80-3, 2-FLUOROPYRIDINE-3-BORONIC ACID HYDRATE, (2-fluoropyridin-3-yl)boronic acid;hydrate, SCHEMBL343330

Application

(2-Fluoropyridin-3-yl)boronic Acid Hydrate is primarily employed in Suzuki-Miyaura cross-coupling reactions to synthesize biaryl and heteroaryl compounds, key intermediates in drug discovery. It is also utilized in the development of fluorinated pyridine derivatives for agrochemical and pharmaceutical applications. Researchers value its stability and reactivity in palladium-catalyzed transformations.

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