This compound is primarily utilized in peptide synthesis as a protecting group for amines. The fluorenylmethyloxycarbonyl (Fmoc) group safeguards the piperidine nitrogen during the synthesis process, preventing unwanted reactions. The tert-butoxycarbonyl (Boc) group, on the other hand, provides additional protection for the 4-amino group of the piperidine, ensuring selective deprotection steps can be carried out. This dual protection strategy is crucial in the stepwise construction of complex peptides, particularly in solid-phase peptide synthesis (SPPS). The compound’s stability under basic conditions and its ability to be selectively removed make it a valuable tool in the production of pharmaceuticals, bioactive peptides, and other organic molecules requiring precise control over chemical reactions.