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CAS 1451393-16-0

:

3-Bromo-2-chloro-6-fluorophenylboronic acid

Description:
3-Bromo-2-chloro-6-fluorophenylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols, making it useful in various organic synthesis applications, particularly in Suzuki coupling reactions. The compound features a phenyl ring substituted with bromine, chlorine, and fluorine atoms, which can influence its reactivity and solubility. The presence of these halogens typically enhances the compound's electrophilicity and can affect its interaction with nucleophiles. Additionally, the boronic acid group contributes to its acidity, allowing it to participate in acid-base reactions. This compound is often utilized in medicinal chemistry and materials science due to its potential in drug development and as a building block for more complex molecules. Its unique combination of halogen substituents may also impart specific electronic properties, making it a subject of interest in research focused on developing new materials or pharmaceuticals.
Formula:C6H4BBrClFO2
Synonyms:
  • 3-Bromo-2-chloro-6-fluorophenylboronic acid
  • 1-Bromo-2-chloro-4-fluoro-3-nitrobenzene
  • Boronic acid, B-(3-bromo-2-chloro-6-fluorophenyl)-
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