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CAS 156545-07-2

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(3,5-Difluorophenyl)boronic acid

Description:
(3,5-Difluorophenyl)boronic 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 3 and 5 positions. This compound typically appears as a white to off-white solid and is soluble in polar organic solvents. It exhibits properties typical of boronic acids, such as the ability to form reversible complexes with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The presence of fluorine atoms can enhance the compound's lipophilicity and influence its reactivity and biological activity. Additionally, (3,5-Difluorophenyl)boronic acid can participate in Suzuki-Miyaura cross-coupling reactions, which are valuable in the formation of carbon-carbon bonds. Its unique structural features make it a subject of interest in the development of pharmaceuticals and agrochemicals, as well as in materials science for creating functionalized polymers and other advanced materials.
Formula:C6H5BF2O2
InChI:InChI=1S/C6H5BF2O2/c8-5-1-4(7(10)11)2-6(9)3-5/h1-3,10-11H
InChI key:InChIKey=QWQBQRYFWNIDOC-UHFFFAOYSA-N
SMILES:B(O)(O)C1=CC(F)=CC(F)=C1
Synonyms:
  • (3,5-Difluorophenyl)boronic acid
  • (3,5-Difluorophenyl)dihydroxyborane
  • (3,5-Dimethoxyphenyl)Boronic Acid
  • 3,5-Difluorobenzeneboronic acid
  • B-(3,5-Difluorophenyl)boronic acid
  • Boronic acid, (3,5-difluorophenyl)-
  • Boronic acid, B-(3,5-difluorophenyl)-
  • Boronic acid，(3,5-difluorophenyl)-(9CI)
  • [4-(Benzyloxy)-2,3-Difluorophenyl]Boronic Acid
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