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CAS 157866-06-3

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Boronic acid, (3-bromo-5-formylphenyl)-

Description:
Boronic acid, specifically (3-bromo-5-formylphenyl)-, is an organoboron compound characterized by the presence of a boronic acid functional group (-B(OH)2) attached to a phenyl ring that also features a bromine atom and a formyl group (-CHO). This compound typically exhibits properties associated with both boronic acids and aromatic aldehydes, including moderate solubility in polar solvents and potential reactivity in various organic transformations. The bromine substituent can enhance electrophilic aromatic substitution reactions, while the formyl group can participate in condensation reactions and serve as a reactive site for further functionalization. Boronic acids are known for their ability to form reversible complexes with diols, making them valuable in synthetic chemistry, particularly in the development of boronate esters and in cross-coupling reactions. The presence of the formyl group also suggests potential applications in the synthesis of more complex organic molecules. Overall, this compound is significant in both academic research and industrial applications, particularly in the fields of organic synthesis and materials science.
Formula:C7H6BBrO3
InChI:InChI=1S/C7H6BBrO3/c9-7-2-5(4-10)1-6(3-7)8(11)12/h1-4,11-12H
InChI key:InChIKey=GPHPTLRDIAKRGQ-UHFFFAOYSA-N
SMILES:B(O)(O)C1=CC(C=O)=CC(Br)=C1
Synonyms:
  • 3-Bromo-5-formylphenylboronic acid
  • (3-Bromo-5-formylphenyl)boronic acid
  • Boronic acid, (3-bromo-5-formylphenyl)-
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