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CAS 1072952-53-4

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B-(3-Chloro-4-formylphenyl)boronic acid

Description:
B-(3-Chloro-4-formylphenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that features both a chloro and a formyl substituent. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The presence of the chloro group enhances its reactivity, while the formyl group introduces an aldehyde functionality, which can participate in further chemical transformations. B-(3-Chloro-4-formylphenyl)boronic acid is often utilized in cross-coupling reactions, particularly in the synthesis of complex organic molecules. Its solubility and stability can vary depending on the solvent and conditions, and it is generally handled with care due to the potential reactivity of the boronic acid moiety. As with many organoboron compounds, it may also exhibit interesting electronic properties, making it a subject of study in materials science and organic electronics.
Formula:C7H6BClO3
InChI:InChI=1S/C7H6BClO3/c9-7-3-6(8(11)12)2-1-5(7)4-10/h1-4,11-12H
InChI key:InChIKey=KDIYVLXLPNHJRZ-UHFFFAOYSA-N
SMILES:B(O)(O)C1=CC(Cl)=C(C=O)C=C1
Synonyms:
  • 3-Chloro-4-formylbenzeneboronic acid
  • 3-Chloro-4-formylphenylboronic acid
  • 4-Borono-2-chlorobenzaldehyde
  • B-(3-Chloro-4-formylphenyl)boronic acid
  • Boronic acid, B-(3-chloro-4-formylphenyl)-
  • Vhr Bg Dbqq
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