tert-butyl trans-3-(hydroxymethyl)-4-(4-isopropylphenyl)pyrrolidine-1-carboxylate

97%

Reagent Code: #242128

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 319.45 g/mol
Formula C₁₉H₂₉NO₃
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 structural features, including the chiral pyrrolidine core and hydroxymethyl group, make it valuable in asymmetric synthesis and medicinal chemistry for constructing complex drug candidates. Commonly employed in the preparation of enzyme inhibitors where stereochemistry and steric bulk influence biological activity. The tert-butyl carbamate (Boc) protection allows for selective functionalization, enabling stepwise assembly of multi-component therapeutics.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿3,960.00
inventory 250mg
10-20 days ฿11,830.00
inventory 1g
10-20 days ฿32,810.00

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tert-butyl trans-3-(hydroxymethyl)-4-(4-isopropylphenyl)pyrrolidine-1-carboxylate
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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 structural features, including the chiral pyrrolidine core and hydroxymethyl group, make it valuable in asymmetric synthesis and medicinal chemistry for constructing complex drug candidates. Commonly employed in the preparation of enzyme inhibitors where stereochemistry and steric bulk influence biological activity. The tert-butyl carbam

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of protease inhibitors and other biologically active molecules. Its structural features, including the chiral pyrrolidine core and hydroxymethyl group, make it valuable in asymmetric synthesis and medicinal chemistry for constructing complex drug candidates. Commonly employed in the preparation of enzyme inhibitors where stereochemistry and steric bulk influence biological activity. The tert-butyl carbamate (Boc) protection allows for selective functionalization, enabling stepwise assembly of multi-component therapeutics.

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