This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction, where it acts as a boronic acid reagent. Its structure, featuring a boronic acid group attached to a 2-fluorophenyl ring that is substituted at the 5-position with a (3,4-dihydroquinolin-1(2H)-yl)methyl group, makes it valuable for constructing complex molecules, especially in pharmaceutical and agrochemical research. The fluorine atom enhances the stability and reactivity of the compound, enabling its use in the development of bioactive molecules. Additionally, it can serve as an intermediate in the synthesis of heterocyclic compounds, which are often explored for their potential therapeutic applications.