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CAS 121219-16-7

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(2,3-Difluorophenyl)boronic acid

Description:
(2,3-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 2 and 3 positions. This compound typically appears as a white to off-white solid and is soluble in polar organic solvents. Its boronic acid functionality allows it to participate in various chemical reactions, particularly in Suzuki coupling reactions, making it valuable in organic synthesis and medicinal chemistry. The presence of fluorine atoms can enhance the compound's lipophilicity and influence its biological activity. Additionally, (2,3-Difluorophenyl)boronic acid can form stable complexes with diols, which is useful in the development of sensors and in the study of biological systems. Its reactivity and functional properties make it a significant compound in the field of pharmaceuticals and materials science. Safety precautions should be observed when handling this compound, as with all boronic acids, due to potential irritant properties.
Formula:C6H5BF2O2
InChI:InChI=1S/C6H5BF2O2/c8-5-3-1-2-4(6(5)9)7(10)11/h1-3,10-11H
InChI key:InChIKey=SZYXKFKWFYUOGZ-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(F)C(F)=CC=C1
Synonyms:
  • (2,3-Difluorophenyl)boronic acid
  • 2,3-Difluorobenzeneboronic Acid
  • 2,3-Difluorobenzeneboronic acid 98%
  • 2,3-Difluorobenzeneboronicacid98%
  • 2,3-Difluorophenylboronic Acid (contains varying amounts of Anhydride)
  • 2,3-Difluorophenylboronic acid, 97+%
  • 2,3-Fluorobenzene Boronic Acid
  • B-(2,3-Difluorophenyl)boronic acid
  • Boronic acid, (2,3-difluorophenyl)-
  • Boronic acid, B-(2,3-difluorophenyl)-
  • Rarechem Ah Pb 0166
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