3-[(tert-butoxycarbonyl)amino]piperidine-3-carboxylic acid

95%

Reagent Code: #242765
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CAS Number 436867-71-9

science Other reagents with same CAS 436867-71-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 244.29 g/mol
Formula C₁₁H₂₀N₂O₄
badge Registry Numbers
MDL Number MFCD02683121
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other biologically active molecules. Its protected amine and carboxylic acid functionalities make it valuable in peptide-like structures and in solid-phase or solution-phase peptide synthesis. Commonly employed in medicinal chemistry for constructing complex nitrogen-containing heterocycles, especially in drug discovery programs targeting metabolic and neurological disorders. The Boc-protected amine allows for selective deprotection and further derivatization, enabling efficient multi-step synthesis.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days $574.41
inventory 1g
10-20 days $1,580.83

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3-[(tert-butoxycarbonyl)amino]piperidine-3-carboxylic acid
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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 molecules. Its protected amine and carboxylic acid functionalities make it valuable in peptide-like structures and in solid-phase or solution-phase peptide synthesis. Commonly employed in medicinal chemistry for constructing complex nitrogen-containing heterocycles, especially in drug discovery programs targeting metabolic and neurological disorders. The Boc

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other biologically active molecules. Its protected amine and carboxylic acid functionalities make it valuable in peptide-like structures and in solid-phase or solution-phase peptide synthesis. Commonly employed in medicinal chemistry for constructing complex nitrogen-containing heterocycles, especially in drug discovery programs targeting metabolic and neurological disorders. The Boc-protected amine allows for selective deprotection and further derivatization, enabling efficient multi-step synthesis.

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