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CAS 913835-76-4

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B-(4-Chloro-2-formylphenyl)boronic acid

Description:
B-(4-Chloro-2-formylphenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that features a chloro substituent and an aldehyde group. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible complexes with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The presence of the chloro group can influence its reactivity and solubility, while the aldehyde functionality may participate in further chemical transformations. B-(4-Chloro-2-formylphenyl)boronic acid is often utilized in Suzuki coupling reactions, which are pivotal in the formation of carbon-carbon bonds. Additionally, its structural features may contribute to its potential biological activity, making it a candidate for further investigation in drug development. As with many boronic acids, it is important to handle this compound with care, considering its reactivity and potential environmental impact.
Formula:C7H6BClO3
InChI:InChI=1S/C7H6BClO3/c9-6-1-2-7(8(11)12)5(3-6)4-10/h1-4,11-12H
InChI key:InChIKey=BTQFQGHQBOWNAJ-UHFFFAOYSA-N
SMILES:C(=O)C1=C(B(O)O)C=CC(Cl)=C1
Synonyms:
  • (4-Chloro-2-formylphenyl)boronic acid
  • 4-Chloro-2-Formylbenzeneboronic Acid
  • 4-Chloro-2-formylphenylboronic acid
  • B-(4-Chloro-2-formylphenyl)boronic acid
  • Boronic acid, (4-chloro-2-formylphenyl)-
  • boronic acid, B-(4-chloro-2-formylphenyl)-
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