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CAS 957120-87-5

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(2,4-dichloro-3-cyano-phenyl)boronic acid

Description:
(2,4-Dichloro-3-cyano-phenyl)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 two chlorine atoms and a cyano group. This compound typically exhibits properties such as being a white to off-white solid, with moderate solubility in polar organic solvents. The presence of the boronic acid group allows it to participate in various chemical reactions, particularly in Suzuki coupling reactions, which are valuable in organic synthesis for forming carbon-carbon bonds. The dichloro and cyano substituents can influence its reactivity and solubility, making it useful in medicinal chemistry and materials science. Additionally, the compound may exhibit interesting electronic properties due to the electron-withdrawing nature of the cyano group and the halogen substituents, which can affect its behavior in biological systems and its potential applications in drug development. Safety data should be consulted for handling and storage, as with all chemical substances.
Formula:C7H4BCl2NO2
InChI:InChI=1/C7H4BCl2NO2/c9-6-2-1-5(8(12)13)7(10)4(6)3-11/h1-2,12-13H
SMILES:c1cc(c(C#N)c(c1B(O)O)Cl)Cl
Synonyms:
  • (2,4-Dichloro-3-cyanophenyl)boronic acid
  • boronic acid, B-(2,4-dichloro-3-cyanophenyl)-
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