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CAS 481725-35-3

:

(4-Acetyl-3-fluorophenyl)boronic acid

Description:
(4-Acetyl-3-fluorophenyl)boronic 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. This compound features a phenyl ring substituted with both an acetyl group and a fluorine atom, contributing to its unique chemical properties. The acetyl group enhances its reactivity and solubility, while the fluorine atom can influence its electronic properties and stability. Typically, boronic acids are utilized in organic synthesis, particularly in Suzuki coupling reactions, which are essential for forming carbon-carbon bonds. The presence of the boronic acid moiety allows for the potential application in medicinal chemistry and materials science. Additionally, the compound may exhibit interesting biological activities due to its structural features, making it a candidate for further research 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:C8H8BFO3
InChI:InChI=1/C8H8BFO3/c1-5(11)7-3-2-6(9(12)13)4-8(7)10/h2-4,12-13H,1H3
SMILES:CC(=O)c1ccc(cc1F)B(O)O
Synonyms:
  • 4-Acetyl-3-fluorobenzeneboronic acid
  • 4-Acetyl-3-fluorophenylboronic acid
  • boronic acid, B-(4-acetyl-3-fluorophenyl)-
  • Qbqr Cf Dv1
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