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CAS 1072944-20-7

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B-[6-(4-Fluorophenyl)-3-pyridinyl]boronic acid

Description:
B-[6-(4-Fluorophenyl)-3-pyridinyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols and is widely used in organic synthesis and medicinal chemistry. This compound features a pyridine ring substituted with a 4-fluorophenyl group, contributing to its unique electronic properties and potential biological activity. The presence of the boronic acid moiety allows for participation in Suzuki-Miyaura cross-coupling reactions, making it valuable in the synthesis of complex organic molecules. Additionally, the fluorine atom enhances the lipophilicity and metabolic stability of the compound, which may influence its pharmacokinetic properties. B-[6-(4-Fluorophenyl)-3-pyridinyl]boronic acid is often studied for its potential applications in drug development, particularly in targeting specific biological pathways or as a building block in the synthesis of pharmaceuticals. Its structural characteristics and reactivity make it a significant compound in both research and industrial applications.
Formula:C11H9BFNO2
InChI:InChI=1S/C11H9BFNO2/c13-10-4-1-8(2-5-10)11-6-3-9(7-14-11)12(15)16/h1-7,15-16H
InChI key:InChIKey=COZZGWRIBKHUFL-UHFFFAOYSA-N
SMILES:B(O)(O)C1=CC=C(N=C1)C2=CC=C(F)C=C2
Synonyms:
  • 6-(4-Fluorophenyl)pyridine-3-boronic acid
  • Boronic acid, B-[6-(4-fluorophenyl)-3-pyridinyl]-
  • (6-(4-Fluorophenyl)pyridin-3-yl)boronic acid
  • B-[6-(4-Fluorophenyl)-3-pyridinyl]boronic acid
  • [6-(4-Fluorophenyl)pyridin-3-yl]boronic acid
  • [6-(4-Fluorophenyl)-3-pyridinyl]boronic acid
  • 6-(4-FLUOROPHENYL)PYRIDIN-3-YLBORONIC ACID
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