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CAS 874290-89-8

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3-Cyanopyridine-4-boronic acid

Description:
3-Cyanopyridine-4-boronic acid is an organic compound characterized by the presence of both a pyridine ring and a boronic acid functional group. Its molecular structure includes a cyano group (-CN) attached to the third carbon of the pyridine ring and a boronic acid group (-B(OH)2) at the fourth position. This compound is typically a white to off-white solid and is soluble in polar solvents such as water and alcohols, owing to the presence of the boronic acid moiety. It is known for its utility in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, which are pivotal in forming carbon-carbon bonds. The boronic acid group can also act as a ligand in coordination chemistry. Additionally, 3-cyanopyridine-4-boronic acid may exhibit biological activity, making it of interest in medicinal chemistry. Its reactivity and functional groups allow for diverse applications in pharmaceuticals and materials science. Proper handling and storage are essential due to its potential reactivity and the need for safety precautions when working with boronic acids.
Formula:C6H5BN2O2
InChI:InChI=1/C6H5BN2O2/c8-3-5-4-9-2-1-6(5)7(10)11/h1-2,4,10-11H
SMILES:c1cncc(C#N)c1B(O)O
Synonyms:
  • (3-Cyanopyridin-4-yl)boronic acid
  • boronic acid, B-(3-cyano-4-pyridinyl)-
  • (3-Cyano-4-Pyridyl)Boronic Acid
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