1-Boc-4-(4-aminophenyl)piperazine

• CAT Number: R030195
• CAS Number: 170911-92-9
• Molecular Formula: C15H23N3O2
• Molecular Weight: 277.36
• Purity: ≥95%
• Synonyms: 4-(4-Aminophenyl)-1-piperazinecarboxylic Acid 1,1-Dimethylethyl Ester; 1-Boc-4-(4’-aminophenyl)piperazine; 1-tert-Butoxycarbonyl-4-(4-aminophenyl)piperidine; 4-(1-tert-Butoxycarbonylpiperazin-4-yl)aniline; 4-(4-(tert-Butoxycarbonyl)piperazin-1-yl)ani
• Storage: Keep in dark place,Inert atmosphere,Room temperature
• IUPAC Name: tert-butyl 4-(4-aminophenyl)piperazine-1-carboxylate
• InChI: InChI=1S/C15H23N3O2/c1-15(2,3)20-14(19)18-10-8-17(9-11-18)13-6-4-12(16)5-7-13/h4-7H,8-11,16H2,1-3H3
• InChIKey: RXFHRKPNLPBDGE-UHFFFAOYSA-N
• SMILES: CC(C)(C)OC(=O)N1CCN(CC1)C2=CC=C(C=C2)N

1-Boc-4-(4-aminophenyl)piperazine (Cat No.:R030195) is a chemical compound. It consists of a piperazine ring with a test-butoxy carbonyl (Boc) protective group attached to a 4-aminophenyl substituent. This compound is essential in medicinal and synthetic chemistry, acting as a key intermediate in drug synthesis. The Boc group protects the amine functionality during chemical transformations, allowing controlled modifications. Its versatile reactivity and role as a building block enable the creation of diverse molecules, particularly in the development of potential pharmaceutical agents. The compound’s structure and reactivity contribute to its significance in drug discovery and chemical research.