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CAS 878194-88-8

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2-Chloro-3-cyanopyridine-4-boronic acid

Description:
2-Chloro-3-cyanopyridine-4-boronic acid is an organic compound characterized by its boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, particularly in organic synthesis and medicinal chemistry. The compound features a pyridine ring substituted with a chlorine atom and a cyano group, contributing to its reactivity and potential biological activity. Its boronic acid moiety allows for participation in Suzuki coupling reactions, a key method for forming carbon-carbon bonds in the synthesis of complex organic molecules. The presence of the cyano group may enhance its electronic properties, influencing its reactivity and interactions with biological targets. This compound is typically handled with care due to the presence of the boronic acid group, which can be sensitive to moisture and air. Overall, 2-Chloro-3-cyanopyridine-4-boronic acid is a valuable intermediate in chemical research and development, particularly in the fields of pharmaceuticals and agrochemicals.
Formula:C6H4BClN2O2
InChI:InChI=1/C6H4BClN2O2/c8-6-4(3-9)5(7(11)12)1-2-10-6/h1-2,11-12H
SMILES:c1cnc(c(C#N)c1B(O)O)Cl
Synonyms:
  • (2-Chloro-3-Cyano-4-Pyridyl)Boronic Acid
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