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CAS 1072946-52-1

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B-(5-Chloro-2-cyanophenyl)boronic acid

Description:
B-(5-Chloro-2-cyanophenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is substituted with a chlorine atom and a cyano group. This compound typically exhibits properties such as being a white to off-white solid, with moderate solubility in polar solvents like water and alcohols, owing to the boronic acid moiety. The presence of the cyano group contributes to its potential as a versatile building block in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, which are widely used in the formation of carbon-carbon bonds. Additionally, the chlorine substituent can influence the electronic properties of the molecule, affecting its reactivity and interactions with other chemical species. B-(5-Chloro-2-cyanophenyl)boronic acid is often utilized in medicinal chemistry and materials science, highlighting its importance in the development of pharmaceuticals and functional materials. Safety data should be consulted for handling and storage, as with all chemical substances.
Formula:C7H5BClNO2
InChI:InChI=1S/C7H5BClNO2/c9-6-2-1-5(4-10)7(3-6)8(11)12/h1-3,11-12H
InChI key:InChIKey=JXIINQQPEHZQAY-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(C#N)C=CC(Cl)=C1
Synonyms:
  • 5-Chloro-2-cyanophenylboronic acid
  • B-(5-Chloro-2-cyanophenyl)boronic acid
  • Boronic acid, B-(5-chloro-2-cyanophenyl)-
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