This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a boronic acid reagent. Its structure, featuring a cyclopentylaminoethoxy group and a fluorine substituent, makes it valuable for constructing complex molecules, especially in pharmaceutical research. The fluorine atom can enhance binding affinity and metabolic stability, making it useful in drug discovery for targeting specific biological pathways. Additionally, the boronic acid moiety facilitates the formation of carbon-carbon bonds, enabling the synthesis of biaryl compounds, which are common in active pharmaceutical ingredients (APIs) and agrochemicals. Its application extends to materials science, where it can be used to modify polymers or create advanced organic materials.