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CAS 1141886-37-4

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B-(5-Chloro-1,6-dihydro-6-oxo-3-pyridinyl)boronic acid

Description:
B-(5-Chloro-1,6-dihydro-6-oxo-3-pyridinyl)boronic acid is a boronic acid derivative characterized by its unique structure, which includes a pyridine ring substituted with a chlorine atom and a keto group. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including medicinal chemistry and organic synthesis. The presence of the chlorine atom can influence its reactivity and solubility, while the boronic acid functional group allows for participation in Suzuki coupling reactions, a key method for forming carbon-carbon bonds. Additionally, this compound may exhibit biological activity, potentially serving as a pharmacophore in drug development. Its stability, solubility, and reactivity can vary depending on the solvent and conditions, making it a versatile compound in research and industrial applications. As with many boronic acids, it is essential to handle this substance with care, considering its potential reactivity and the need for proper storage conditions.
Formula:C5H5BClNO3
InChI:InChI=1S/C5H5BClNO3/c7-4-1-3(6(10)11)2-8-5(4)9/h1-2,10-11H,(H,8,9)
InChI key:InChIKey=LOJWDAMORQDVBQ-UHFFFAOYSA-N
SMILES:B(O)(O)C=1C=C(Cl)C(=O)NC1
Synonyms:
  • Boronic acid, B-(5-chloro-1,6-dihydro-6-oxo-3-pyridinyl)-
  • B-(5-Chloro-1,6-dihydro-6-oxo-3-pyridinyl)boronic acid
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