(2-Fluoro-5-hydroxyphenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that also contains a fluorine atom and a hydroxyl group. This compound typically exhibits a white to off-white crystalline appearance. The boronic acid moiety allows for the formation of reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The presence of the fluorine atom can enhance the compound's lipophilicity and influence its biological activity, while the hydroxyl group contributes to its solubility in polar solvents. Additionally, this compound may participate in Suzuki-Miyaura cross-coupling reactions, which are valuable in the formation of carbon-carbon bonds. Its unique structural features make it a candidate for further research in drug development and materials science. As with many boronic acids, it is important to handle this compound with care due to potential reactivity and toxicity.

(2-fluoro-5-hydroxyphenyl)boronic acid

1150114-52-5: (2-Fluoro-5-hydroxyphenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that also contains a fluorine atom and a hydroxyl group. This compound typically exhibits a white to off-white crystalline appearance. The boronic acid moiety allows for the formation of reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The presence of the fluorine atom can enhance the compound's lipophilicity and influence its biological activity, while the hydroxyl group contributes to its solubility in polar solvents. Additionally, this compound may participate in Suzuki-Miyaura cross-coupling reactions, which are valuable in the formation of carbon-carbon bonds. Its unique structural features make it a candidate for further research in drug development and materials science. As with many boronic acids, it is important to handle this compound with care due to potential reactivity and toxicity.

CAS 1150114-52-5

(2-fluoro-5-hydroxyphenyl)boronic acid

Boronic acid, B-(2-fluoro-5-hydroxyphenyl)-

Ref: IN-DA000FMP

2-Fluoro-5-hydroxyphenylboronic acid

Ref: 54-PC412425

(2-Fluoro-5-hydroxyphenyl)boronic acid

Ref: 10-F209184