Used primarily as an intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boronate ester group readily reacts with aryl or heteroaryl halides in the presence of a palladium catalyst, making it valuable in pharmaceutical and agrochemical research. The tert-butyl carbamate (Boc) protecting group stabilizes the amine functionality during reaction sequences and can be easily removed under mild acidic conditions when needed. This dual functionality allows for selective and stepwise construction of nitrogen-containing heterocyclic systems, commonly found in bioactive compounds and drug candidates.