Used in organic synthesis as a key intermediate for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical development. The boronate ester group facilitates coupling with aryl or heteroaryl halides under palladium catalysis, making it valuable for constructing complex molecules, particularly in drug discovery. The ester functionality allows for further transformations, such as hydrolysis or reduction, to modify the scaffold for specific biological activity. Its stability and reactivity profile make it suitable for use in late-stage functionalization of bioactive compounds.