CAS 1451390-81-0
:B-(3-Acetyl-2,6-difluorophenyl)boronic acid
Description:
B-(3-Acetyl-2,6-difluorophenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is further substituted with an acetyl group and two fluorine atoms. This compound typically exhibits properties such as moderate solubility in organic solvents and potential reactivity in cross-coupling reactions, making it valuable in organic synthesis and medicinal chemistry. The presence of the boronic acid moiety allows for participation in Suzuki-Miyaura coupling reactions, which are essential for forming carbon-carbon bonds. The difluorophenyl substituent may influence the electronic properties and steric hindrance of the molecule, potentially affecting its reactivity and interactions with biological targets. Additionally, the acetyl group can serve as a site for further functionalization or modification. Overall, B-(3-Acetyl-2,6-difluorophenyl)boronic acid is a versatile compound with applications in drug development and materials science, particularly in the synthesis of complex organic molecules.
Formula:C8H7BF2O3
InChI:InChI=1S/C8H7BF2O3/c1-4(12)5-2-3-6(10)7(8(5)11)9(13)14/h2-3,13-14H,1H3
InChI key:InChIKey=MOLKUWDTTSLAMM-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(F)C(C(C)=O)=CC=C1F
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