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(1S,3R,4R)-2-[(tert-butoxy)carbonyl]-2-azabicyclo[2.2.1]heptane-3-carboxylic acid; CAS No.: 291775-53-6; (1S,3R,4R)-2-Boc-2-azabicyclo[2.2.1]heptane-3-carboxylic acid exemplifies our bridged bicyclic amino acids for peptide stapling applications. The norbornane-type structure induces rigid helical conformations in peptides. As a leading chemicals distributor, we provide enantiomerically pure bicyclic scaffolds. The carboxylic acid and Boc-protected amine enable solid-phase peptide synthesis integration. Our manufacturing process utilizes catalytic asymmetric hydrogenation for stereochemical control.