(R)-3-(Boc-amino)piperidine

• CAT Number: R029178
• CAS Number: 309956-78-3
• Molecular Formula: C10H20N2O2
• Molecular Weight: 200.28
• Purity: ≥95%
• Synonyms: (3R)-3-Piperidinyl-carbamic Acid 1,1-Dimethylethyl Ester; (3R)-3-[((tert-Butyloxycarbonyl)amino)]piperidine; (R)-3-(tert-Butoxycarbonylamino)piperidine; (R)-3-[(tert-Butoxycarbonyl)amino]piperidine; (R)-3-[(tert-Butyloxycarbonyl)amino]piperidine; (R)
• Storage: -20°C
• IUPAC Name: tert-butyl N-[(3R)-piperidin-3-yl]carbamate
• InChI: InChI=1S/C10H20N2O2/c1-10(2,3)14-9(13)12-8-5-4-6-11-7-8/h8,11H,4-7H2,1-3H3,(H,12,13)/t8-/m1/s1
• InChIKey: WUOQXNWMYLFAHT-MRVPVSSYSA-N
• SMILES: CC(C)(C)OC(=O)N[C@@H]1CCCNC1

(R)-3-(Boc-amino)piperidine（Cat No.:R029178）is a chiral, protected piperidine derivative featuring a tert-butoxycarbonyl (Boc) group on the amino function at the 3-position of the piperidine ring. The (R)-configuration denotes its specific stereochemistry, which is important for enantioselective synthesis and pharmaceutical development. The Boc group serves as a common protecting group in peptide and organic synthesis, providing stability during multi-step reactions and easily removable under acidic conditions. This compound is widely used as a building block in medicinal chemistry for the synthesis of drug candidates, chiral auxiliaries, and complex nitrogen-containing heterocycles.