[3-(Dimethylcarbamoyl)-5-fluoro-phenyl]boronic acid is an organic compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols, making it useful in various applications such as organic synthesis and medicinal chemistry. The compound features a phenyl ring substituted with a fluorine atom and a dimethylcarbamoyl group, which contributes to its chemical reactivity and potential biological activity. The presence of the boronic acid moiety allows for participation in Suzuki coupling reactions, a key method for forming carbon-carbon bonds in organic synthesis. Additionally, the dimethylcarbamoyl group may enhance solubility and influence the compound's interaction with biological targets. Overall, this compound's unique structural features make it a valuable candidate for research in drug development and materials science, particularly in the context of developing new therapeutic agents or advanced materials. Its specific properties, such as solubility, stability, and reactivity, would depend on the conditions under which it is used.

[3-(dimethylcarbamoyl)-5-fluoro-phenyl]boronic acid

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(3-(Dimethylcarbamoyl)-5-fluorophenyl)boronic acid

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CAS 874219-39-3: [3-(dimethylcarbamoyl)-5-fluoro-phenyl]boronic acid

(3-(Dimethylcarbamoyl)-5-fluorophenyl)boronic acid

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(3-(Dimethylcarbamoyl)-5-fluorophenyl)boronic acid

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3-(Dimethylcarbamoyl)-5-fluorobenzeneboronic acid

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[3-(dimethylcarbamoyl)-5-fluorophenyl]boronic Acid

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