This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling, which forms carbon-carbon bonds between aryl boronate and aryl halide compounds. The 4,4,5,5-tetramethyl-1,3,2-dioxaborolane group enhances the stability and efficiency of the boronate ester, making it a valuable intermediate for constructing complex organic molecules. Additionally, the tert-butyl carbamate group protects the amine functionality during synthesis, enabling selective transformations. It is especially employed in pharmaceutical research and development for synthesizing biologically active compounds, including drug candidates. Its stability and reactivity under mild conditions make it a preferred choice in various catalytic processes.