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CAS 497147-93-0

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5-cyano-3-pyridinyl boronic acid

Description:
5-Cyano-3-pyridinyl boronic acid is an organic compound characterized by the presence of a pyridine ring substituted with a cyano group and a boronic acid functional group. The boronic acid moiety is known for its ability to form reversible covalent bonds with diols, making it valuable in various applications, including organic synthesis and medicinal chemistry. The cyano group contributes to the compound's electronic properties, enhancing its reactivity and potential interactions with biological targets. This compound is typically a solid at room temperature and is soluble in polar solvents, which facilitates its use in chemical reactions. Its unique structure allows it to participate in cross-coupling reactions, particularly in the formation of carbon-carbon bonds, which is a crucial step in the synthesis of complex organic molecules. Additionally, the presence of both the cyano and boronic acid groups may impart specific biological activities, making it a subject of interest in drug discovery and development. Overall, 5-cyano-3-pyridinyl boronic acid is a versatile compound with significant implications in both synthetic and medicinal chemistry.
Formula:C6H5BN2O2
InChI:InChI=1/C6H5BN2O2/c8-2-5-1-6(7(10)11)4-9-3-5/h1,3-4,10-11H
SMILES:c1c(C#N)cncc1B(O)O
Synonyms:
  • (5-Cyanopyridin-3-yl)boronic acid
  • 5-Cyanopyridine-3-boronic acid
  • 5-Cyanopyridin-3-Ylboronic Acid
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