3-Cyclohexylcarbamoyl-4-fluorobenzeneboronic acid is primarily utilized in organic synthesis and medicinal chemistry. Its boronic acid functional group makes it a valuable intermediate in Suzuki-Miyaura cross-coupling reactions, which are widely employed to construct carbon-carbon bonds in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. The cyclohexylcarbamoyl moiety enhances its potential as a building block for designing drug candidates, particularly in the development of enzyme inhibitors or receptor modulators. The fluorine atom in the aromatic ring can influence the compound's binding affinity and metabolic stability, making it useful in the optimization of bioactive molecules. Additionally, its structural features make it a candidate for research in material science, particularly in the development of advanced organic materials or sensors.