Description

tert-Butyl (1,4′-bipiperidin-4-ylmethyl)-carbamate (CAS No. 883512-84-3) is a high-purity organic compound with the molecular formula C₁₆H₃₁N₃O₂. This specialized chemical features a bipiperidinyl backbone protected by a tert-butoxycarbonyl (Boc) group, making it a valuable intermediate in pharmaceutical and medicinal chemistry research. With an IUPAC name of tert-butyl N-[(1-piperidin-4-ylpiperidin-4-yl)methyl]carbamate, this compound is characterized by its dual piperidine rings and carbamate functionality, offering versatile reactivity for further synthetic modifications. Ideal for drug discovery applications, it is supplied with comprehensive analytical data including HPLC, NMR, and mass spectrometry to ensure quality and consistency. Store under inert conditions at recommended temperatures to maintain stability.

Properties

• CAS Number: 883512-84-3
• Complexity: 327
• IUPAC Name: tert-butyl N-[[1-(4-piperidyl)-4-piperidyl]methyl]carbamate
• InChI: InChI=1S/C16H31N3O2/c1-16(2,3)21-15(20)18-12-13-6-10-19(11-7-13)14-4-8-17-9-5-14/h13-14,17H,4-12H2,1-3H3,(H,18,20)
• InChI Key: YOQSKBHJINOZQI-UHFFFAOYSA-N
• Exact Mass: 297.24162724
• Molecular Formula: C16H31N3O2
• Molecular Weight: 297.44
• SMILES: CC(C)(C)OC(=O)NCC1CCN(CC1)C2CCNCC2
• Topological: 53.6
• Monoisotopic Mass: 297.24162724
• Synonyms: 883512-84-3, tert-Butyl (1,4′-bipiperidin-4-ylmethyl)-carbamate, tert-Butyl ([1,4′-bipiperidin]-4-ylmethyl)carbamate, tert-butyl N-[(1-piperidin-4-ylpiperidin-4-yl)methyl]carbamate, tert-butyl (1-(piperidin-4-yl) piperidin-4-yl)methylcarbamate, DTXSID70629565, AKOS003658006, DB-077253, F88169, tert-Butyl([1,4′-bipiperidin]-4-ylmethyl)carbamate, tert-Butyl [([1,4′-bipiperidin]-4-yl)methyl]carbamate, 4-(4-Methylaminopiperidin-1-yl, 4-BOC protected)piperidine

Application

This compound serves as a key building block in the synthesis of bioactive molecules, particularly in the development of CNS-targeting pharmaceuticals. Researchers utilize its bipiperidinyl structure to modulate pharmacokinetic properties in drug candidates. The Boc-protected amine allows for selective deprotection in multi-step synthetic routes. It has shown utility in creating analogs for receptor binding studies and enzyme inhibition assays.

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