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CAS 1451391-43-7

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B-(4-Cyano-2,6-dimethylphenyl)boronic acid

Description:
B-(4-Cyano-2,6-dimethylphenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a substituted aromatic ring. The compound features a cyano group (-CN) and two methyl groups (-CH3) on the phenyl ring, which influence its chemical reactivity and solubility. Boronic acids are known for their ability to form reversible complexes with diols, making them valuable in organic synthesis, particularly in Suzuki coupling reactions for the formation of carbon-carbon bonds. The cyano group contributes to the compound's electronic properties, potentially enhancing its reactivity in nucleophilic addition reactions. Additionally, the presence of the methyl groups can affect steric hindrance and the overall stability of the molecule. This compound may find applications in medicinal chemistry, materials science, and as a building block in the synthesis of more complex organic molecules. Its specific properties, such as melting point, solubility, and reactivity, would need to be determined through experimental characterization.
Formula:C9H10BNO2
InChI:InChI=1S/C9H10BNO2/c1-6-3-8(5-11)4-7(2)9(6)10(12)13/h3-4,12-13H,1-2H3
InChI key:InChIKey=JTJKZJPBCISPOI-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(C)C=C(C#N)C=C1C
Synonyms:
  • 4-Cyano-2,6-dimethylphenylboronic acid
  • B-(4-Cyano-2,6-dimethylphenyl)boronic acid
  • (4-Cyano-2,6-dimethylphenyl)boronic acid
  • Boronic acid, B-(4-cyano-2,6-dimethylphenyl)-
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