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CAS 1217500-67-8

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B-(3-Chloro-2-cyanophenyl)boronic acid

Description:
B-(3-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 contains both a chlorine atom and a cyano group. This compound typically appears as a solid and is soluble in polar organic solvents. The boronic acid moiety allows for participation in various chemical reactions, particularly in Suzuki coupling reactions, which are widely used in organic synthesis for forming carbon-carbon bonds. The presence of the chloro and cyano substituents on the phenyl ring can influence the reactivity and selectivity of the compound in synthetic applications. Additionally, boronic acids are known for their ability to form reversible complexes with diols, making them useful in the development of sensors and in medicinal chemistry. Safety data sheets should be consulted for handling and storage guidelines, as boronic acids can be sensitive to moisture and may pose health risks if not handled properly.
Formula:C7H5BClNO2
InChI:InChI=1S/C7H5BClNO2/c9-7-3-1-2-6(8(11)12)5(7)4-10/h1-3,11-12H
InChI key:InChIKey=NVFNOKJQOOUGTR-UHFFFAOYSA-N
SMILES:C(#N)C1=C(B(O)O)C=CC=C1Cl
Synonyms:
  • (3-Chloro-2-cyanophenyl)boronic acid
  • Boronic acid, B-(3-chloro-2-cyanophenyl)-
  • B-(3-Chloro-2-cyanophenyl)boronic acid
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