This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a boronic acid reagent. Its structure, featuring a boronic acid group and a fluorine substituent, makes it valuable for constructing complex molecules, especially in pharmaceutical research. The tert-butoxycarbonyl (Boc) protecting group enhances its stability during reactions, allowing for selective deprotection when needed. Applications include the development of drug candidates, agrochemicals, and advanced materials, where precise control over molecular architecture is essential. Its cyclopropyl moiety can also impart unique steric and electronic properties to the final products, influencing their biological activity or material performance.