1-N-Cbz-4-N-(Boc-Aminomethyl)Piperidine

≥97%

Reagent Code: #217462
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CAS Number 172348-56-0

science Other reagents with same CAS 172348-56-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 348.44 g/mol
Formula C₁₉H₂₈N₂O₄
thermostat Physical Properties
Boiling Point 484.5ºC
inventory_2 Storage & Handling
Density 1.117 g/cm3
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and other bioactive molecules. Its protected amine functionalities allow for selective reactions in multi-step organic syntheses, especially in peptide and peptidomimetic chemistry. The Cbz and Boc protecting groups provide stability during reactions and can be selectively removed under mild conditions, making this compound valuable in solid-phase and solution-phase peptide synthesis. It is also employed in the preparation of receptor ligands and enzyme inhibitors where a piperidine scaffold is required for structural rigidity and binding specificity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,070.00
inventory 25g
10-20 days ฿13,150.00
inventory 5g
10-20 days ฿3,710.00
1-N-Cbz-4-N-(Boc-Aminomethyl)Piperidine
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and other bioactive molecules. Its protected amine functionalities allow for selective reactions in multi-step organic syntheses, especially in peptide and peptidomimetic chemistry. The Cbz and Boc protecting groups provide stability during reactions and can be selectively removed under mild conditions, making this compound valuable in solid-phase and solution-phase peptide synt

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and other bioactive molecules. Its protected amine functionalities allow for selective reactions in multi-step organic syntheses, especially in peptide and peptidomimetic chemistry. The Cbz and Boc protecting groups provide stability during reactions and can be selectively removed under mild conditions, making this compound valuable in solid-phase and solution-phase peptide synthesis. It is also employed in the preparation of receptor ligands and enzyme inhibitors where a piperidine scaffold is required for structural rigidity and binding specificity.

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