(2S,4R)-1-(tert-Butoxycarbonyl)-4-methoxypyrrolidine-2-carboxylicacid

96%

Reagent Code: #237907
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CAS Number 83624-01-5

science Other reagents with same CAS 83624-01-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 245.27 g/mol
Formula C₁₁H₁₉NO₅
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MDL Number MFCD11847488
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other biologically active compounds. Its stereochemistry makes it valuable for constructing complex molecules with high enantioselectivity. Commonly employed in medicinal chemistry for peptidomimetic design, where the pyrrolidine ring mimics proline to influence peptide conformation and stability. The Boc-protected amine and carboxylic acid functionalities allow for straightforward incorporation into larger molecular frameworks through standard coupling reactions. Also utilized in the preparation of enzyme inhibitors and central nervous system agents due to its structural rigidity and compatibility with diverse synthetic pathways.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,840.00
inventory 250mg
10-20 days ฿6,400.00
inventory 500mg
10-20 days ฿10,660.00
inventory 5g
10-20 days ฿48,000.00
inventory 10g
10-20 days ฿80,000.00
inventory 1g
10-20 days ฿16,000.00

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(2S,4R)-1-(tert-Butoxycarbonyl)-4-methoxypyrrolidine-2-carboxylicacid
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other biologically active compounds. Its stereochemistry makes it valuable for constructing complex molecules with high enantioselectivity. Commonly employed in medicinal chemistry for peptidomimetic design, where the pyrrolidine ring mimics proline to influence peptide conformation and stability. The Boc-protected amine and carboxylic acid functionalities allow for straightforward incorporation into larger molecular frameworks through standard coupling reactions. Also utilized in the preparation of enzyme inhibitors and central nervous system agents due to its structural rigidity and compatibility with diverse synthetic pathways.
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