tert-Butyl (R)-3-Aminopiperidine-1-carboxylate

• CAT Number: R022673
• CAS Number: 188111-79-7
• Molecular Formula: C10H20N2O2
• Molecular Weight: 200.28
• Purity: ≥95%
• Synonyms: (3R)-3-Amino-1-piperidinecarboxylic Acid 1,1-Dimethylethyl Ester; (R)-1-tert-Butoxycarbonyl-3-aminopiperidine; (R)-1-tert-Butoxycarbonyl-3-aminopiperidine; (R)-3-Amino-1-Boc-piperidine; (R)-3-Aminopiperidine-1-carboxylic Acid tert-Butyl Ester; (R)-3-
• Storage: Store at RT
• IUPAC Name: tert-butyl (3R)-3-aminopiperidine-1-carboxylate
• InChI: InChI=1S/C10H20N2O2/c1-10(2,3)14-9(13)12-6-4-5-8(11)7-12/h8H,4-7,11H2,1-3H3/t8-/m1/s1
• InChIKey: AKQXKEBCONUWCL-MRVPVSSYSA-N
• SMILES: CC(C)(C)OC(=O)N1CCCC(C1)N

tert-Butyl (R)-3-aminopiperidine-1-carboxylate (Cat No.: R022673) is a chiral, nitrogen-containing heterocyclic compound used as an intermediate in pharmaceutical synthesis. It features a piperidine ring with an amino group at the 3-position in the (R)-configuration and a tert-butoxycarbonyl (Boc) protecting group on the nitrogen atom. The Boc group enhances the compound’s chemical stability and allows for selective deprotection under acidic conditions. This compound is particularly valuable in the synthesis of biologically active molecules, including central nervous system agents and enzyme inhibitors, due to its stereochemical control.