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CAS 957060-96-7

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B-(2-Chloro-5-cyano-3-pyridinyl)boronic acid

Description:
B-(2-Chloro-5-cyano-3-pyridinyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a pyridine ring that contains both a chlorine and a cyano substituent. This compound typically exhibits properties common to boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The presence of the cyano group enhances its reactivity and potential for further functionalization. Additionally, the chlorine atom can influence the compound's electronic properties and solubility. B-(2-Chloro-5-cyano-3-pyridinyl)boronic acid may also exhibit biological activity, making it a candidate for research in drug development. Its structural features suggest potential applications in the synthesis of complex organic molecules and in the development of boron-containing pharmaceuticals. As with many boronic acids, it is important to handle this compound with care, considering its reactivity and potential environmental impact.
Formula:C6H4BClN2O2
InChI:InChI=1S/C6H4BClN2O2/c8-6-5(7(11)12)1-4(2-9)3-10-6/h1,3,11-12H
InChI key:InChIKey=JOXTUWQJEBJZEK-UHFFFAOYSA-N
SMILES:B(O)(O)C=1C=C(C#N)C=NC1Cl
Synonyms:
  • B-(2-Chloro-5-cyano-3-pyridinyl)boronic acid
  • Boronic acid, B-(2-chloro-5-cyano-3-pyridinyl)-
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