4-Cbz-Aminopiperidine

97%

Reagent Code: #159416
label
Alias 4-(Cbz-amino)piperidine; 4-CBZ-aminopiperidine;
fingerprint
CAS Number 182223-54-7

science Other reagents with same CAS 182223-54-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 234.29 g/mol
Formula C₁₃H₁₈N₂O₂
badge Registry Numbers
MDL Number MFCD04038571
thermostat Physical Properties
Boiling Point 396.3ºC
inventory_2 Storage & Handling
Density 1.13g/cm3
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other biologically active compounds. Its protected amine group allows for selective reactions in multi-step organic syntheses, making it valuable in medicinal chemistry. Commonly employed in the preparation of HIV protease inhibitors and kinase inhibitors due to its structural compatibility with enzyme binding sites. Also utilized in solid-phase peptide synthesis and as a building block in combinatorial chemistry for drug discovery.

Available Sizes & Pricing

Size Availability Unit Price Quantity
5g
10-20 days ฿2,240.00
10g
10-20 days ฿4,440.00
25g
10-20 days ฿9,760.00
100g
10-20 days ฿38,520.00
4-Cbz-Aminopiperidine
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other biologically active compounds. Its protected amine group allows for selective reactions in multi-step organic syntheses, making it valuable in medicinal chemistry. Commonly employed in the preparation of HIV protease inhibitors and kinase inhibitors due to its structural compatibility with enzyme binding sites. Also utilized in solid-phase peptide synthesis and as a building bl

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other biologically active compounds. Its protected amine group allows for selective reactions in multi-step organic syntheses, making it valuable in medicinal chemistry. Commonly employed in the preparation of HIV protease inhibitors and kinase inhibitors due to its structural compatibility with enzyme binding sites. Also utilized in solid-phase peptide synthesis and as a building block in combinatorial chemistry for drug discovery.

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