(2S,4S)-1-(tert-Butoxycarbonyl)-4-phenoxypyrrolidine-2-carboxylic acid

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Reagent Code: #36581
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CAS Number 147266-79-3

science Other reagents with same CAS 147266-79-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 307.34 g/mol
Formula C₁₆H₂₁NO₅
badge Registry Numbers
MDL Number MFCD06656447
thermostat Physical Properties
Boiling Point 455.8°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This compound is primarily utilized in the synthesis of pharmaceuticals, particularly as an intermediate in the production of complex organic molecules. Its structure, featuring both a tert-butoxycarbonyl (Boc) protecting group and a carboxylic acid moiety, makes it valuable in peptide synthesis and medicinal chemistry. The Boc group can be selectively removed under mild acidic conditions, allowing for further functionalization of the molecule. Additionally, the presence of the phenoxy group enhances its potential for creating biologically active compounds, such as enzyme inhibitors or receptor modulators, due to its ability to interact with aromatic binding sites in proteins. This chemical is often employed in research and development settings to explore new drug candidates or optimize existing therapeutic agents.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,917.00

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(2S,4S)-1-(tert-Butoxycarbonyl)-4-phenoxypyrrolidine-2-carboxylic acid
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This compound is primarily utilized in the synthesis of pharmaceuticals, particularly as an intermediate in the production of complex organic molecules. Its structure, featuring both a tert-butoxycarbonyl (Boc) protecting group and a carboxylic acid moiety, makes it valuable in peptide synthesis and medicinal chemistry. The Boc group can be selectively removed under mild acidic conditions, allowing for further functionalization of the molecule. Additionally, the presence of the phenoxy group enhances its

This compound is primarily utilized in the synthesis of pharmaceuticals, particularly as an intermediate in the production of complex organic molecules. Its structure, featuring both a tert-butoxycarbonyl (Boc) protecting group and a carboxylic acid moiety, makes it valuable in peptide synthesis and medicinal chemistry. The Boc group can be selectively removed under mild acidic conditions, allowing for further functionalization of the molecule. Additionally, the presence of the phenoxy group enhances its potential for creating biologically active compounds, such as enzyme inhibitors or receptor modulators, due to its ability to interact with aromatic binding sites in proteins. This chemical is often employed in research and development settings to explore new drug candidates or optimize existing therapeutic agents.

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