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711002-74-3

3-Amino-1-N-Cbz-piperidine

Catalog#: AR005P4X  |   CAS#: 711002-74-3  |   MDL#: MFCD03001672  |   MF: C13H18N2O2  |   MW: 234.2942

Packsize Purity Price Availability Quantity
250mg 97% $7.00 Global Stock Buy Now Add To Cart
1g 97% $15.00 Global Stock Buy Now Add To Cart
5g 97% $48.00 Global Stock Buy Now Add To Cart
10g 97% $78.00 Global Stock Buy Now Add To Cart
25g 97% $174.00 Global Stock Buy Now Add To Cart
100g 97% $520.00 Global Stock Buy Now Add To Cart
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Catalog Number AR005P4X
Chemical Name 3-Amino-1-N-Cbz-piperidine
CAS Number 711002-74-3
Molecular Formula C13H18N2O2
Molecular Weight 234.2942
MDL Number MFCD03001672
SMILES NC1CCCN(C1)C(=O)OCc1ccccc1

3-Amino-1-N-Cbz-piperidine, also known as Cbz-protected 3-aminopiperidine, is a versatile building block in organic synthesis. Its primary application lies in the field of medicinal chemistry and drug development, where it serves as a key intermediate for the synthesis of various biologically active compounds.One of the main uses of 3-Amino-1-N-Cbz-piperidine is in the synthesis of pharmaceutical agents targeting the central nervous system. By incorporating this compound into the molecular structure of drug candidates, chemists can enhance their interactions with specific biological targets, leading to improved pharmacological properties and therapeutic effects. Additionally, the Cbz protecting group on the amino group provides stability during synthetic transformations, allowing for selective functionalization at other reactive sites within the molecule.Furthermore, 3-Amino-1-N-Cbz-piperidine is employed in the preparation of peptidomimetics and peptide-based therapeutics. Through strategic modifications and conjugations with amino acids or peptide sequences, researchers can design novel compounds with enhanced biological activity, improved stability, and selective targeting capabilities. This application broadens the scope of peptide drug discovery and provides alternative strategies for overcoming limitations associated with traditional peptide structures.In chemical synthesis, the versatility of 3-Amino-1-N-Cbz-piperidine enables the construction of complex molecules with diverse functionalities. Its compatibility with various synthetic methodologies, including amide coupling, hydrogenation, and deprotection reactions, makes it a valuable tool for building intricate molecular architectures. As a result, this compound plays a pivotal role in the creation of diverse chemical libraries for exploring structure-activity relationships and identifying lead compounds in drug discovery programs.
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