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CAS 144025-03-6

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2,4-Difluorophenylboronic acid

Description:
2,4-Difluorophenylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that has two fluorine substituents at the 2 and 4 positions. This compound typically appears as a white to off-white solid and is soluble in polar solvents such as water and alcohols, owing to the boronic acid group, which can form hydrogen bonds. The presence of fluorine atoms enhances its electronic properties, making it useful in various applications, including medicinal chemistry and materials science. It can participate in Suzuki-Miyaura cross-coupling reactions, which are pivotal in the synthesis of biaryl compounds. Additionally, 2,4-difluorophenylboronic acid can act as a ligand in coordination chemistry and is of interest in the development of sensors and drug delivery systems due to its ability to interact with biological molecules. Safety precautions should be taken when handling this compound, as with many organoboron compounds, due to potential toxicity and reactivity.
Formula:C6H5BF2O2
InChI:InChI=1S/C6H5BF2O2/c8-4-1-2-5(7(10)11)6(9)3-4/h1-3,10-11H
InChI key:InChIKey=QQLRSCZSKQTFGY-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(F)C=C(F)C=C1
Synonyms:
  • 2,4-Difluorophenyl-1-boronic acid
  • 2,4-Difluorophenyl-Boronic Acid
  • 2,4-Difluorophenylboronic acid
  • B-(2,4-Difluorophenyl)boronic acid
  • Boronic acid, (2,4-difluorophenyl)-
  • Boronic acid, B-(2,4-difluorophenyl)-
  • 2,4-Difluorobenzeneboronic acid
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