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CAS 762287-58-1

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2-Fluoro-3-methylphenylboronic acid

Description:
2-Fluoro-3-methylphenylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is substituted with both a fluorine atom and a methyl group. This compound typically exhibits a white to off-white solid appearance 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 the fluorine atom can influence the electronic properties of the molecule, potentially enhancing its reactivity in various chemical reactions, including Suzuki coupling reactions, which are widely used in organic synthesis. Additionally, the methyl group can affect the steric and electronic environment around the boron atom, influencing its reactivity and interactions with other molecules. 2-Fluoro-3-methylphenylboronic acid is utilized in medicinal chemistry and materials science, particularly in the development of pharmaceuticals and functional materials due to its ability to form stable complexes with diols and other nucleophiles.
Formula:C7H8BFO2
InChI:InChI=1S/C7H8BFO2/c1-5-3-2-4-6(7(5)9)8(10)11/h2-4,10-11H,1H3
InChI key:InChIKey=VEHQHYJZLSODOU-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(F)C(C)=CC=C1
Synonyms:
  • 2-Fluoro-3-Tolylboronic Acid
  • 2-Fluoro-3-methylphenylboronic acid
  • B-(2-Fluoro-3-methylphenyl)boronic acid
  • Boronic acid, (2-fluoro-3-methylphenyl)-
  • boronic acid, B-(2-fluoro-3-methylphenyl)-
  • (2-Fluoro-3-methylphenyl)boronic acid
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