3-[[(Tert-Butoxy)Carbonyl]Amino]-1-Piperidinecarboxylic Acid Tert-Butyl Ester

≥97%

Reagent Code: #241032
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CAS Number 1217710-80-9

science Other reagents with same CAS 1217710-80-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 300.39 g/mol
Formula C₁₅H₂₈N₂O₄
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a protected diamine building block in peptide synthesis and medicinal chemistry. The compound contains two Boc (tert-butoxycarbonyl) protecting groups—one on a piperidine nitrogen and another on an amino group—making it ideal for selective deprotection and stepwise construction of complex molecules. Commonly employed in the synthesis of pharmaceuticals, especially protease inhibitors and kinase inhibitors, where controlled amine reactivity is required. Its stability under various reaction conditions allows for use in multi-step organic transformations, including coupling reactions and heterocycle formation. Also utilized in the development of APIs (active pharmaceutical ingredients) requiring masked amine functionalities.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿830.00
inventory 5g
10-20 days ฿3,450.00
inventory 10g
10-20 days ฿6,550.00
inventory 25g
10-20 days ฿15,030.00

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3-[[(Tert-Butoxy)Carbonyl]Amino]-1-Piperidinecarboxylic Acid Tert-Butyl Ester
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Used as a protected diamine building block in peptide synthesis and medicinal chemistry. The compound contains two Boc (tert-butoxycarbonyl) protecting groups—one on a piperidine nitrogen and another on an amino group—making it ideal for selective deprotection and stepwise construction of complex molecules. Commonly employed in the synthesis of pharmaceuticals, especially protease inhibitors and kinase inhibitors, where controlled amine reactivity is required. Its stability under various reaction conditi

Used as a protected diamine building block in peptide synthesis and medicinal chemistry. The compound contains two Boc (tert-butoxycarbonyl) protecting groups—one on a piperidine nitrogen and another on an amino group—making it ideal for selective deprotection and stepwise construction of complex molecules. Commonly employed in the synthesis of pharmaceuticals, especially protease inhibitors and kinase inhibitors, where controlled amine reactivity is required. Its stability under various reaction conditions allows for use in multi-step organic transformations, including coupling reactions and heterocycle formation. Also utilized in the development of APIs (active pharmaceutical ingredients) requiring masked amine functionalities.

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