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CAS 2121513-74-2

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B-(6-Fluoro-2-hydroxy-3-methylphenyl)boronic acid

Description:
B-(6-Fluoro-2-hydroxy-3-methylphenyl)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 a fluorine atom and hydroxyl and methyl groups. This compound typically exhibits properties such as being a white to off-white solid, with moderate solubility in polar solvents like water and alcohols due to the presence of the hydroxyl group. The boronic acid moiety allows for participation in various chemical reactions, including Suzuki coupling, making it valuable in organic synthesis and medicinal chemistry. Its fluorine substitution can enhance biological activity and lipophilicity, while the hydroxyl group may contribute to hydrogen bonding interactions. The compound's structure suggests potential applications in drug development, particularly in the design of inhibitors or modulators of biological targets. As with many boronic acids, it may also exhibit sensitivity to moisture and air, necessitating careful handling and storage conditions.
Formula:C7H8BFO3
InChI:InChI=1S/C7H8BFO3/c1-4-2-3-5(9)6(7(4)10)8(11)12/h2-3,10-12H,1H3
InChI key:InChIKey=NWMPBVGNPGAQAS-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(O)C(C)=CC=C1F
Synonyms:
  • B-(6-Fluoro-2-hydroxy-3-methylphenyl)boronic acid
  • Boronic acid, B-(6-fluoro-2-hydroxy-3-methylphenyl)-
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