trans-1-(tert-butoxycarbonyl)-4-(2,5-difluorophenyl)pyrrolidine-3-carboxylic acid

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Reagent Code: #241942
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CAS Number 2227727-31-1

science Other reagents with same CAS 2227727-31-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 327.33 g/mol
Formula C₁₆H₁₉F₂NO₄
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of protease inhibitors and other biologically active molecules. Its structure supports the construction of complex drug candidates requiring stereochemical control and functional group compatibility. Commonly employed in medicinal chemistry for building blocks in peptidomimetics and enzyme inhibitors, especially in treatments targeting metabolic and viral diseases. The Boc-protected amine and carboxylic acid functionalities allow for sequential coupling reactions, making it valuable in solid-phase and solution-phase synthesis of drug-like compounds.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿10,260.00
inventory 1g
10-20 days ฿28,800.00
inventory 100mg
10-20 days ฿5,840.00

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trans-1-(tert-butoxycarbonyl)-4-(2,5-difluorophenyl)pyrrolidine-3-carboxylic acid
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of protease inhibitors and other biologically active molecules. Its structure supports the construction of complex drug candidates requiring stereochemical control and functional group compatibility. Commonly employed in medicinal chemistry for building blocks in peptidomimetics and enzyme inhibitors, especially in treatments targeting metabolic and viral diseases. The Boc-protected amine and carboxylic

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of protease inhibitors and other biologically active molecules. Its structure supports the construction of complex drug candidates requiring stereochemical control and functional group compatibility. Commonly employed in medicinal chemistry for building blocks in peptidomimetics and enzyme inhibitors, especially in treatments targeting metabolic and viral diseases. The Boc-protected amine and carboxylic acid functionalities allow for sequential coupling reactions, making it valuable in solid-phase and solution-phase synthesis of drug-like compounds.

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