Used primarily in organic synthesis as a key intermediate in Suzuki-Miyaura cross-coupling reactions. The compound enables the formation of carbon-carbon bonds, particularly in the construction of complex molecules such as pharmaceuticals and agrochemicals. Its allylic boronate ester group facilitates efficient coupling with aryl or vinyl halides under palladium catalysis. 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 makes it valuable in multi-step synthesis of nitrogen-containing target compounds, including bioactive molecules and functional materials.