CymitQuimica logo

CAS 870777-29-0

:

2-Fluoro-5-acetylphenylboronic acid

Description:
2-Fluoro-5-acetylphenylboronic 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 applications, including organic synthesis and medicinal chemistry. This compound features a phenyl ring substituted with a fluorine atom at the 2-position and an acetyl group at the 5-position, contributing to its unique reactivity and properties. The presence of the boronic acid group allows for participation in Suzuki-Miyaura cross-coupling reactions, facilitating the formation of carbon-carbon bonds. Additionally, the fluorine atom can influence the electronic properties of the molecule, potentially enhancing its reactivity or selectivity in chemical reactions. The compound is typically a solid at room temperature and may exhibit solubility in polar organic solvents. Its applications may extend to drug development, where boronic acids are often explored for their potential in targeting specific biological pathways. Safety and handling precautions should be observed, as with all chemical substances, due to potential hazards associated with boron compounds and fluorinated materials.
Formula:C8H8BFO3
InChI:InChI=1S/C8H8BFO3/c1-5(11)6-2-3-8(10)7(4-6)9(12)13/h2-4,12-13H,1H3
InChI key:InChIKey=FQVNUEBNRAIKBR-UHFFFAOYSA-N
SMILES:B(O)(O)C1=CC(C(C)=O)=CC=C1F
Synonyms:
  • 2-Fluoro-5-Acetylphenylboronic Acid
  • 5-Acetyl-2-fluorobenzeneboronic acid
  • 5-Acetyl-2-fluorophenylboronic acid
  • B-(5-Acetyl-2-fluorophenyl)boronic acid
  • Boronic acid, (5-acetyl-2-fluorophenyl)-
  • Boronic acid, B-(5-acetyl-2-fluorophenyl)-
  • (5-Acetyl-2-fluorophenyl)boronic acid
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 4 products.