1-Boc-4-(6-aminopyridin-3-yl)piperazine

• CAT Number: R026556
• CAS Number: 571188-59-5
• Molecular Formula: C14H22N4O2
• Molecular Weight: 278.36
• Purity: ≥95%
• Synonyms: 4-(6-Aminopyridin-3-yl)piperazine-1-carboxylic Acid tert-Butyl Ester; 4-(6-Aminopyridin-3-yl)piperazine-1-carboxylic Acid tert-Butyl Ester; tert-Butyl 4-(6-Amino-3-pyridyl)piperazine-1-carboxylate; tert-Butyl 4-(6-Aminopyridin-3-yl)piperazine-1-carbo
• Storage: -20°C
• IUPAC Name: tert-butyl 4-(6-aminopyridin-3-yl)piperazine-1-carboxylate
• InChI: InChI=1S/C14H22N4O2/c1-14(2,3)20-13(19)18-8-6-17(7-9-18)11-4-5-12(15)16-10-11/h4-5,10H,6-9H2,1-3H3,(H2,15,16)
• InChIKey: RMULRXHUNOVPEI-UHFFFAOYSA-N
• SMILES: CC(C)(C)OC(=O)N1CCN(CC1)C2=CN=C(C=C2)N

1-Boc-4-(6-aminopyridin-3-yl)piperazine（Cat No.:R026556）is a synthetic organic compound featuring a piperazine ring substituted with a 6-aminopyridin-3-yl group and protected by a tert-butoxycarbonyl (Boc) group. The Boc group safeguards the piperazine nitrogen during chemical reactions, allowing selective transformations. This compound is commonly used as a building block in medicinal chemistry, especially in the design of kinase inhibitors, CNS-active agents, and other bioactive molecules. Its structure provides multiple functional sites for derivatization, making it valuable in drug discovery, lead optimization, and structure-activity relationship (SAR) studies in pharmaceutical research.