1-Fmoc-4-piperidone

≥97%

Reagent Code: #187850
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CAS Number 204376-55-6

science Other reagents with same CAS 204376-55-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 321.37 g/mol
Formula C₂₀H₁₉NO₃
badge Registry Numbers
MDL Number MFCD00673794
thermostat Physical Properties
Boiling Point 510.4ºC
inventory_2 Storage & Handling
Density 1.255g/cm3
Storage 2-8ºC

description Product Description

Used primarily in organic synthesis and medicinal chemistry, this compound serves as a key building block for the preparation of piperidine-containing pharmaceuticals. Its Fmoc-protected amine group allows for selective deprotection under mild basic conditions, making it highly suitable for solid-phase peptide synthesis and the construction of complex heterocyclic systems. It is widely employed in the development of drug candidates targeting central nervous system disorders, including pain management and neurodegenerative diseases. The ketone functionality provides a handle for further chemical modifications such as reductive amination or nucleophilic addition, enabling rapid diversification in library synthesis for drug discovery.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿540.00
inventory 5g
10-20 days ฿2,320.00
inventory 25g
10-20 days ฿10,500.00

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1-Fmoc-4-piperidone
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Used primarily in organic synthesis and medicinal chemistry, this compound serves as a key building block for the preparation of piperidine-containing pharmaceuticals. Its Fmoc-protected amine group allows for selective deprotection under mild basic conditions, making it highly suitable for solid-phase peptide synthesis and the construction of complex heterocyclic systems. It is widely employed in the development of drug candidates targeting central nervous system disorders, including pain management and neurodegenerative diseases. The ketone functionality provides a handle for further chemical modifications such as reductive amination or nucleophilic addition, enabling rapid diversification in library synthesis for drug discovery.
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