(2-Fluoro-6-methoxypyridin-3-yl)boronic acid is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is widely employed in the pharmaceutical industry to create carbon-carbon bonds, enabling the synthesis of complex molecules, including drug candidates and bioactive compounds. The boronic acid group in this compound acts as a key reagent, facilitating the coupling with aryl or vinyl halides in the presence of a palladium catalyst. Its fluorine and methoxy substituents can influence the reactivity and selectivity of the reaction, making it valuable for constructing specific molecular architectures. Additionally, it may be utilized in the development of agrochemicals, materials science, and other fine chemical industries where precise molecular design is critical.