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CAS 138642-62-3

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2-Cyanophenylboronic acid

Description:
2-Cyanophenylboronic acid is an organoboron compound characterized by the presence of both 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 ring that is further substituted with a cyano group at the ortho position. This compound is typically used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, which are valuable for forming carbon-carbon bonds. The presence of the cyano group enhances its reactivity and solubility in various organic solvents. 2-Cyanophenylboronic acid is also known for its potential applications in medicinal chemistry, particularly in the development of pharmaceuticals. It is important to handle this compound with care, as boronic acids can be sensitive to moisture and air, which may affect their stability and reactivity. Overall, 2-Cyanophenylboronic acid is a versatile building block in synthetic organic chemistry, contributing to the advancement of various chemical processes and applications.
Formula:C7H6BNO2
InChI:InChI=1S/C7H6BNO2/c9-5-6-3-1-2-4-7(6)8(10)11/h1-4,10-11H
InChI key:InChIKey=NPLZNDDFVCGRAG-UHFFFAOYSA-N
SMILES:C(#N)C1=C(B(O)O)C=CC=C1
Synonyms:
  • 2-Cyanobenzeneboronic acid
  • 2-Cyanophenylboronic acid
  • B-(2-Cyanophenyl)boronic acid
  • Boronic acid, (2-cyanophenyl)-
  • Boronic acid, B-(2-cyanophenyl)-
  • [m-Cyanophenyl-4-yl]boronic acid
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