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CAS 903899-13-8

:

(6-Oxo-1,6-dihydropyridin-3-yl)boronic acid

Description:
(6-Oxo-1,6-dihydropyridin-3-yl)boronic acid, with the CAS number 903899-13-8, is a boronic acid derivative characterized by the presence of a pyridine ring and a boronic acid functional group. This compound typically exhibits properties associated with both boronic acids and heterocyclic compounds. It is likely to be a white to off-white solid, soluble in polar solvents such as water and alcohols, due to the presence of the boronic acid moiety, which can engage in hydrogen bonding and coordination with other molecules. The compound may participate in various chemical reactions, including Suzuki coupling, which is significant in organic synthesis for forming carbon-carbon bonds. Additionally, the presence of the keto group in the pyridine ring can influence its reactivity and stability. Its potential applications may extend to medicinal chemistry, particularly in the development of pharmaceuticals, due to the biological activity often associated with boronic acids. As with many boronic acids, it may also exhibit pH-dependent behavior, affecting its solubility and reactivity in different environments.
Formula:C5H6BNO3
InChI:InChI=1S/C5H6BNO3/c8-5-2-1-4(3-7-5)6(9)10/h1-3,9-10H,(H,7,8)
InChI key:InChIKey=YUOLAYZNDYRBEZ-UHFFFAOYSA-N
SMILES:B(O)(O)C=1C=CC(=O)NC1
Synonyms:
  • (6-Oxo-1,6-dihydropyridin-3-yl)boronic acid
  • (6-Oxo-1H-pyridin-3-yl)boronic acid
  • 2-Hydroxy-5-pyridineboronic acid
  • 2-Hydroxylpyridine-5-Boronic Acid
  • 6-Hydroxypyridin-3-ylboronic acid
  • 6-Hydroxypyridin-3-ylboronicacid
  • 6-Hydroxypyridine-3-boronic acid
  • B-(1,6-Dihydro-6-oxo-3-pyridinyl)boronic acid
  • Boronic acid, (1,6-dihydro-6-oxo-3-pyridinyl)-
  • Boronic acid, B-(1,6-dihydro-6-oxo-3-pyridinyl)-
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