Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its rigid bicyclic structure helps enforce specific three-dimensional orientations that enhance binding selectivity and potency in drug candidates. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to the stability and functional handle provided by the Boc-protected amine and carboxylic acid group. Facilitates peptide-like coupling reactions and is valuable in creating libraries for high-throughput screening.