1-Boc-3-aminopiperidine

98%

Reagent Code: #144478
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CAS Number 144243-24-3

science Other reagents with same CAS 144243-24-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 201.22 g/mol
Formula C₉H₁₅NO₄
badge Registry Numbers
MDL Number MFCD01861219
inventory_2 Storage & Handling
Storage Room temperature, sealed

description Product Description

Used in pharmaceutical synthesis as a protected amine building block, particularly in the development of active pharmaceutical ingredients (APIs). The Boc group protects the piperidine nitrogen, allowing selective reactivity at the 3-amino position and enabling controlled coupling reactions in multi-step syntheses. Commonly employed in the preparation of kinase inhibitors, CNS-active compounds, and other bioactive molecules where the piperidine scaffold is required. Its stability under various reaction conditions makes it suitable for use in combinatorial chemistry and parallel synthesis.

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Test Parameter Specification
Appearance Colorless to pale yellow oil
Purity (%) 97.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿980.00
inventory 5g
10-20 days ฿3,250.00
inventory 25g
10-20 days ฿10,880.00

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1-Boc-3-aminopiperidine
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Used in pharmaceutical synthesis as a protected amine building block, particularly in the development of active pharmaceutical ingredients (APIs). The Boc group protects the piperidine nitrogen, allowing selective reactivity at the 3-amino position and enabling controlled coupling reactions in multi-step syntheses. Commonly employed in the preparation of kinase inhibitors, CNS-active compounds, and other bioactive molecules where the piperidine scaffold is required. Its stability under various reaction c

Used in pharmaceutical synthesis as a protected amine building block, particularly in the development of active pharmaceutical ingredients (APIs). The Boc group protects the piperidine nitrogen, allowing selective reactivity at the 3-amino position and enabling controlled coupling reactions in multi-step syntheses. Commonly employed in the preparation of kinase inhibitors, CNS-active compounds, and other bioactive molecules where the piperidine scaffold is required. Its stability under various reaction conditions makes it suitable for use in combinatorial chemistry and parallel synthesis.

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