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

97%

Reagent Code: #242131

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 333.47 g/mol
Formula C₂₀H₃₁NO₃
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used primarily in pharmaceutical research as an intermediate in the synthesis of bioactive molecules. Its rigid pyrrolidine scaffold and functional groups make it valuable for developing compounds with specific stereochemistry, particularly in central nervous system agents and receptor modulators. The tert-butyl and hydroxymethyl groups allow further chemical modifications, enabling optimization of pharmacokinetic properties such as metabolic stability and membrane permeability. It is also employed in the development of protease inhibitors and receptor antagonists due to its structural similarity to proline derivatives and its ability to influence peptide conformation.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿10,210.00
inventory 1g
10-20 days ฿32,810.00

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tert-butyl trans-3-(4-(tert-butyl)phenyl)-4-(hydroxymethyl)pyrrolidine-1-carboxylate
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Used primarily in pharmaceutical research as an intermediate in the synthesis of bioactive molecules. Its rigid pyrrolidine scaffold and functional groups make it valuable for developing compounds with specific stereochemistry, particularly in central nervous system agents and receptor modulators. The tert-butyl and hydroxymethyl groups allow further chemical modifications, enabling optimization of pharmacokinetic properties such as metabolic stability and membrane permeability. It is also employed in th

Used primarily in pharmaceutical research as an intermediate in the synthesis of bioactive molecules. Its rigid pyrrolidine scaffold and functional groups make it valuable for developing compounds with specific stereochemistry, particularly in central nervous system agents and receptor modulators. The tert-butyl and hydroxymethyl groups allow further chemical modifications, enabling optimization of pharmacokinetic properties such as metabolic stability and membrane permeability. It is also employed in the development of protease inhibitors and receptor antagonists due to its structural similarity to proline derivatives and its ability to influence peptide conformation.

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