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CAS 1315339-48-0

:

B-(2-Bromo-4,6-difluorophenyl)boronic acid

Description:
B-(2-Bromo-4,6-difluorophenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is substituted with bromine and fluorine atoms. This compound typically exhibits properties such as being a white to off-white solid, with moderate solubility in polar organic solvents. The presence of the boronic acid group allows it to participate in various chemical reactions, particularly in Suzuki coupling reactions, which are widely used in organic synthesis for forming carbon-carbon bonds. The bromine and fluorine substituents on the phenyl ring can influence the compound's reactivity and stability, as well as its electronic properties. Additionally, boronic acids are known for their ability to form reversible complexes with diols, which can be exploited in various applications, including drug delivery and sensor technology. Overall, B-(2-Bromo-4,6-difluorophenyl)boronic acid is a valuable compound in synthetic organic chemistry and materials science.
Formula:C6H4BBrF2O2
InChI:InChI=1S/C6H4BBrF2O2/c8-4-1-3(9)2-5(10)6(4)7(11)12/h1-2,11-12H
InChI key:InChIKey=POXLFROUJDNFPQ-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(Br)C=C(F)C=C1F
Synonyms:
  • 2,4-Difluoro-6-bromophenylboronic acid
  • B-(2-Bromo-4,6-difluorophenyl)boronic acid
  • Boronic acid, B-(2-bromo-4,6-difluorophenyl)-
  • (2-Bromo-4,6-difluorophenyl)boronic acid
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