(3-((2-(Dimethylamino)ethyl)carbamoyl)-5-fluorophenyl)boronic acid
98%
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This compound is primarily utilized in organic synthesis and medicinal chemistry as a key intermediate in the development of pharmaceuticals. Its boronic acid functional group makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely used to form carbon-carbon bonds in the synthesis of complex organic molecules, including drug candidates. The presence of the fluorine atom enhances its potential in designing bioactive compounds, as fluorine is often incorporated into drugs to improve metabolic stability and binding affinity. Additionally, the dimethylaminoethyl group can contribute to the molecule's solubility and interaction with biological targets, making it useful in the design of receptor-targeted therapies. Its applications are particularly relevant in the development of anticancer and antiviral agents, where precise molecular modifications are critical for efficacy.
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