N-tert-Butoxycarbonyl-4-anilinopiperidine

• CAT Number: R050480
• CAS Number: 125541-22-2
• Molecular Formula: C16H24N2O2
• Molecular Weight: 276.38
• Purity: ≥95%
• Synonyms: 4-(Phenylamino)-1-piperidinecarboxylic Acid 1,1-Dimethylethyl Ester; 4-Phenylaminopiperidine-1-carboxylic Acid tert-Butyl Ester; 1-(tert-Butyloxycarbonyl)-4-(phenylamino)piperidine
• Storage: Room temperature
• IUPAC Name: tert-butyl 4-anilinopiperidine-1-carboxylate
• InChI: InChI=1S/C16H24N2O2/c1-16(2,3)20-15(19)18-11-9-14(10-12-18)17-13-7-5-4-6-8-13/h4-8,14,17H,9-12H2,1-3H3
• InChIKey: HTIWISWAPVQGMI-UHFFFAOYSA-N
• SMILES: CC(C)(C)OC(=O)N1CCC(CC1)NC2=CC=CC=C2

N-tert-Butoxycarbonyl-4-anilinopiperidine is a chemical compound commonly used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals. The tert-butoxycarbonyl (Boc) group serves as a protective group for the amine, allowing selective reactions to occur without affecting the nitrogen atom. 4-Anilinopiperidine is a structural motif often found in drug development, especially in the synthesis of opioid receptor ligands and analgesics. By protecting the amine group, N-tert-Butoxycarbonyl-4-anilinopiperidine facilitates various chemical modifications, making it a valuable building block in medicinal chemistry for the development of therapeutic agents.