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CAS 874290-88-7

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2-Cyanopyridine-3-boronic acid

Description:
2-Cyanopyridine-3-boronic acid, with the CAS number 874290-88-7, is an organoboron compound characterized by the presence of both a boronic acid functional group and a cyano group attached to a pyridine ring. This compound typically appears as a solid and is soluble in polar solvents such as water and alcohols, owing to the presence of the boronic acid group, which can participate in hydrogen bonding. It is known for its utility in organic synthesis, particularly in cross-coupling reactions, such as Suzuki-Miyaura reactions, where it acts as a boron source. The cyano group contributes to its reactivity and can participate in various chemical transformations. Additionally, 2-cyanopyridine-3-boronic acid may exhibit biological activity, making it of interest in medicinal chemistry. Its stability under standard conditions is generally good, but it should be handled with care due to the potential reactivity of the boronic acid moiety. Overall, this compound serves as a valuable building block in both synthetic and medicinal chemistry applications.
Formula:C6H5BN2O2
InChI:InChI=1/C6H5BN2O2/c8-4-6-5(7(10)11)2-1-3-9-6/h1-3,10-11H
SMILES:c1cc(c(C#N)nc1)B(O)O
Synonyms:
  • (2-Cyanopyridin-3-yl)boronic acid
  • boronic acid, B-(2-cyano-3-pyridinyl)-
  • (2-Cyano-3-Pyridyl)Boronic Acid
  • 2-Cyanopyridin-3-Ylboronic Acid
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