The compound (4-(Dimethylcarbamoyl)-2-fluorophenyl)boronic acid, also known as $name$, serves as a versatile chemical building block in organic synthesis. This molecule is utilized as a key reagent in the formation of carbon-carbon and carbon-heteroatom bonds, making it an essential tool in the field of medicinal chemistry, agrochemical development, and material science. Specifically, (4-(Dimethylcarbamoyl)-2-fluorophenyl)boronic acid is commonly employed in Suzuki-Miyaura cross-coupling reactions to introduce the 2-fluorophenyl moiety into complex molecular structures. This reaction enables the selective and efficient construction of biaryl compounds, which are prevalent in pharmaceuticals and fine chemical production. The presence of the boronic acid functionality in the molecule further enhances its utility by allowing for further derivatization and modification through diverse metal-catalyzed coupling methodologies. Moreover, the (dimethylcarbamoyl) group provides steric hindrance and electronic effects that can influence reactivity and selectivity in various synthetic transformations. Overall, the strategic placement of functional groups in the structure of (4-(Dimethylcarbamoyl)-2-fluorophenyl)boronic acid facilitates its integration into complex molecular architectures, making it an indispensable tool for chemical synthesis endeavors.
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