Methyl 2-((tert-butoxycarbonyl)amino)-2-(piperidin-4-yl)acetate

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Reagent Code: #207252
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CAS Number 219832-76-5

science Other reagents with same CAS 219832-76-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 272.34 g/mol
Formula C₁₃H₂₄N₂O₄
badge Registry Numbers
MDL Number MFCD04115491
inventory_2 Storage & Handling
Storage 2-8°C

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 structure allows for selective modification in peptide-based drug design, making it valuable in medicinal chemistry research. Commonly employed in solid-phase and solution-phase peptide synthesis due to the presence of protected amine and carboxylic ester functionalities. The Boc-protected amine ensures stability during reactions, while the ester group can be hydrolyzed or coupled to extend molecular complexity. Frequently utilized in the preparation of kinase inhibitors and central nervous system agents.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿2,440.00
inventory 250mg
10-20 days ฿7,360.00

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Methyl 2-((tert-butoxycarbonyl)amino)-2-(piperidin-4-yl)acetate
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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 structure allows for selective modification in peptide-based drug design, making it valuable in medicinal chemistry research. Commonly employed in solid-phase and solution-phase peptide synthesis due to the presence of protected amine and carboxylic ester functionalities. The Boc-protected amine ensures stability during reactions, while the es

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other biologically active compounds. Its structure allows for selective modification in peptide-based drug design, making it valuable in medicinal chemistry research. Commonly employed in solid-phase and solution-phase peptide synthesis due to the presence of protected amine and carboxylic ester functionalities. The Boc-protected amine ensures stability during reactions, while the ester group can be hydrolyzed or coupled to extend molecular complexity. Frequently utilized in the preparation of kinase inhibitors and central nervous system agents.

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