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CAS 870779-02-5

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(2,6-difluoro-3-methoxyphenyl)boronic acid

Description:
(2,6-Difluoro-3-methoxyphenyl)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 two fluorine atoms and a methoxy group. This compound typically exhibits a white to off-white solid appearance and is soluble 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 essential in organic synthesis for forming carbon-carbon bonds. The fluorine substituents can influence the electronic properties of the molecule, potentially enhancing its reactivity and stability. Additionally, the methoxy group can serve as a directing group in electrophilic aromatic substitution reactions. Overall, (2,6-difluoro-3-methoxyphenyl)boronic acid is valuable in medicinal chemistry and materials science due to its unique structural features and reactivity.
Formula:C7H7BF2O3
InChI:InChI=1/C7H7BF2O3/c1-13-5-3-2-4(9)6(7(5)10)8(11)12/h2-3,11-12H,1H3
SMILES:COc1ccc(c(c1F)B(O)O)F
Synonyms:
  • Boronic acid, B-(2,6-difluoro-3-methoxyphenyl)-
  • 2,6-Difluoro-3-Methoxybenzeneboronic Acid
  • (2,6-Difluoro-3-methoxyphenyl)boronic acid
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