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CAS 126747-14-6

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4-Cyanophenylboronic acid

Description:
4-Cyanophenylboronic acid is an organic compound characterized by the presence of a boronic acid functional group and a cyano group attached to a phenyl ring. Its molecular structure features a boron atom bonded to a hydroxyl group and a phenyl group that is further substituted with a cyano group at the para 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 exhibits properties that make it useful in various applications, including organic synthesis, particularly in Suzuki coupling reactions, where it acts as a coupling partner for the formation of biaryl compounds. Additionally, the cyano group enhances its electronic properties, making it valuable in materials science and medicinal chemistry. 4-Cyanophenylboronic acid is also known for its ability to form reversible complexes with diols, which is significant in the development of sensors and drug delivery systems.
Formula:C7H6BNO2
InChI:InChI=1S/C7H6BNO2/c9-5-6-1-3-7(4-2-6)8(10)11/h1-4,10-11H
InChI key:InChIKey=CEBAHYWORUOILU-UHFFFAOYSA-N
SMILES:B(O)(O)C1=CC=C(C#N)C=C1
Synonyms:
  • (4-Cyanophenyl)Boronic Acid
  • (p-Cyanophenyl)boronic acid
  • 4-Boronobenzonitrile
  • 4-Cyanobenzeneboronic Acid
  • 4-Cyanophenylboric acid
  • B-(4-Cyanophenyl)boronic acid
  • Boronic acid, (4-cyanophenyl)-
  • Boronic acid, (4-cyanophenyl)- (9CI)
  • Boronic acid, B-(4-cyanophenyl)-
  • P-Cyanophenylboronic Acid
  • 4-Cyanophenylboronic acid
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