This compound is primarily used in organic synthesis as an intermediate in the preparation of more complex molecules. Its structure, featuring a spiro[3.3]heptane core, makes it valuable for constructing rigid frameworks in medicinal chemistry, particularly in drug discovery. The tert-butoxycarbonyl (Boc) group serves as a protective group for amines, allowing selective reactions to occur at other sites of the molecule. The methyl ester functionality can be hydrolyzed to a carboxylic acid, enabling further derivatization. It is often employed in the development of peptidomimetics and small molecule inhibitors, where the spirocyclic system contributes to enhanced stability and bioavailability. Additionally, its unique geometry is explored in materials science for designing novel polymers or supramolecular assemblies.