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CAS 1451390-80-9

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B-(3-Acetyl-6-bromo-2-fluorophenyl)boronic acid

Description:
B-(3-Acetyl-6-bromo-2-fluorophenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its reactivity in various organic synthesis applications, particularly in Suzuki coupling reactions. This compound features a phenyl ring substituted with an acetyl group, a bromine atom, and a fluorine atom, contributing to its unique electronic and steric properties. The acetyl group can enhance the compound's solubility and reactivity, while the halogen substituents (bromine and fluorine) can influence its reactivity and stability. Boronic acids are typically used in medicinal chemistry and materials science due to their ability to form stable complexes with diols and their role in cross-coupling reactions. The presence of multiple functional groups in B-(3-Acetyl-6-bromo-2-fluorophenyl)boronic acid suggests potential applications in the synthesis of complex organic molecules and pharmaceuticals. Additionally, the compound's specific structural features may allow for selective interactions in biological systems, making it a candidate for further research in drug development.
Formula:C8H7BBrFO3
InChI:InChI=1S/C8H7BBrFO3/c1-4(12)5-2-3-6(10)7(8(5)11)9(13)14/h2-3,13-14H,1H3
InChI key:InChIKey=WVFYJYHNIWIUOI-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(F)C(C(C)=O)=CC=C1Br
Synonyms:
  • B-(3-Acetyl-6-bromo-2-fluorophenyl)boronic acid
  • Boronic acid, B-(3-acetyl-6-bromo-2-fluorophenyl)-
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