1-(tert-Butoxycarbonyl)-4-oxopyrrolidine-2-carboxylic acid

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Reagent Code: #146112
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CAS Number 876317-19-0

science Other reagents with same CAS 876317-19-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 229.23 g/mol
Formula C₁₀H₁₅NO₅
thermostat Physical Properties
Melting Point 155°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) involving pyrrolidine-based structures. The tert-butoxycarbonyl (Boc) group protects the pyrrolidine nitrogen, enabling selective modifications in multi-step organic syntheses and efficient deprotection under mild acidic conditions. This makes it valuable in medicinal chemistry for building complex molecules, including in peptide synthesis and the preparation of protease inhibitors, CNS-active agents, and other bioactive compounds requiring controlled ring structures and protected functional groups.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿960.00
inventory 5g
10-20 days ฿4,770.00
inventory 25g
10-20 days ฿21,780.00
inventory 100g
10-20 days ฿72,000.00
inventory 10g
10-20 days ฿8,920.00

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1-(tert-Butoxycarbonyl)-4-oxopyrrolidine-2-carboxylic acid
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) involving pyrrolidine-based structures. The tert-butoxycarbonyl (Boc) group protects the pyrrolidine nitrogen, enabling selective modifications in multi-step organic syntheses and efficient deprotection under mild acidic conditions. This makes it valuable in medicinal chemistry for building complex molecules, including in peptide synthesis and the preparation of p
Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) involving pyrrolidine-based structures. The tert-butoxycarbonyl (Boc) group protects the pyrrolidine nitrogen, enabling selective modifications in multi-step organic syntheses and efficient deprotection under mild acidic conditions. This makes it valuable in medicinal chemistry for building complex molecules, including in peptide synthesis and the preparation of protease inhibitors, CNS-active agents, and other bioactive compounds requiring controlled ring structures and protected functional groups.
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