4-Amino-1-N-Fmoc-piperidine hydrochloride

98%

Reagent Code: #138292
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CAS Number 811841-89-1

science Other reagents with same CAS 811841-89-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 358.86 g/mol
Formula C₂₀H₂₃ClN₂O₂
badge Registry Numbers
MDL Number MFCD03001675
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used in peptide synthesis and medicinal chemistry as a protected amino piperidine building block. The Fmoc group allows for orthogonal protection in solid-phase synthesis, enabling stepwise assembly of complex molecules. Commonly employed in the development of pharmaceuticals, particularly in the design of bioactive compounds targeting central nervous system receptors. Its structure provides a constrained scaffold that enhances selectivity and metabolic stability in drug candidates. Widely utilized in combinatorial chemistry for generating diverse compound libraries.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿4,720.00
inventory 5g
10-20 days ฿16,480.00
inventory 25g
10-20 days ฿67,260.00

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4-Amino-1-N-Fmoc-piperidine hydrochloride
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Used in peptide synthesis and medicinal chemistry as a protected amino piperidine building block. The Fmoc group allows for orthogonal protection in solid-phase synthesis, enabling stepwise assembly of complex molecules. Commonly employed in the development of pharmaceuticals, particularly in the design of bioactive compounds targeting central nervous system receptors. Its structure provides a constrained scaffold that enhances selectivity and metabolic stability in drug candidates. Widely utilized in co

Used in peptide synthesis and medicinal chemistry as a protected amino piperidine building block. The Fmoc group allows for orthogonal protection in solid-phase synthesis, enabling stepwise assembly of complex molecules. Commonly employed in the development of pharmaceuticals, particularly in the design of bioactive compounds targeting central nervous system receptors. Its structure provides a constrained scaffold that enhances selectivity and metabolic stability in drug candidates. Widely utilized in combinatorial chemistry for generating diverse compound libraries.

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