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CAS 867333-43-5

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(5-Cyano-2-methylphenyl)boronic acid

Description:
(5-Cyano-2-methylphenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that also contains a cyano and a methyl substituent. This compound typically exhibits properties such as being a white to off-white solid at room temperature, with solubility in polar solvents like water and alcohols due to the boronic acid group. 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 cyano group enhances the electron-withdrawing characteristics of the phenyl ring, potentially influencing its reactivity and interaction with other chemical species. Additionally, boronic acids are known for their ability to form reversible complexes with diols, which can be exploited in various applications, including sensor technology and drug delivery systems. Overall, (5-Cyano-2-methylphenyl)boronic acid serves as a valuable building block in synthetic organic chemistry.
Formula:C8H8BNO2
InChI:InChI=1S/C8H8BNO2/c1-6-2-3-7(5-10)4-8(6)9(11)12/h2-4,11-12H,1H3
SMILES:Cc1ccc(cc1B(O)O)C#N
Synonyms:
  • Boronic acid, (5-cyano-2-methylphenyl)-
  • Boronicacid,B-(5-cyano-2-methylphenyl)-
  • 5-Cyano-2-methylphenylboronic acid
  • (5-Cyano-2-methylphenyl)boronic acid 97%
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