[4-Fluoro-3-[methoxy(methyl)carbamoyl]phenyl]boronic acid, with the CAS number 874290-69-4, is a boronic acid derivative characterized by its unique functional groups that include a fluorine atom, a methoxy group, and a carbamoyl moiety. This compound typically exhibits properties associated with boronic acids, such as the ability to form 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 biological activity, while the methoxy and carbamoyl groups may influence its solubility and reactivity. Additionally, boronic acids are known for their role in Suzuki coupling reactions, which are pivotal in the formation of carbon-carbon bonds in organic synthesis. Overall, this compound's structural features suggest potential utility in drug development and materials science, particularly in the design of targeted therapies or as intermediates in synthetic pathways.

[4-fluoro-3-[methoxy(methyl)carbamoyl]phenyl]boronic acid

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(4-Fluoro-3-(methoxy(methyl)carbamoyl)phenyl)boronic acid

4-Fluoro-3-[(N-methoxy-N-methyl)carbamoyl]benzeneboronic acid

4-FLUORO-3-(METHOXY(METHYL)CARBAMOYL)PHENYLBORONIC ACID

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CAS 874290-69-4: [4-fluoro-3-[methoxy(methyl)carbamoyl]phenyl]boronic acid

(4-Fluoro-3-(methoxy(methyl)carbamoyl)phenyl)boronic acid

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4-Fluoro-3-[(N-methoxy-N-methyl)carbamoyl]benzeneboronic acid

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4-FLUORO-3-(METHOXY(METHYL)CARBAMOYL)PHENYLBORONIC ACID

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{4-Fluoro-3-[methoxy(methyl)carbamoyl]phenyl}boronic acid

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