(2S,4S)-1-Tert-Butyl 2-Methyl 4-((Tert-Butyldimethylsilyl)Oxy)Pyrrolidine-1,2-Dicarboxylate

98%

Reagent Code: #123619
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CAS Number 367966-45-8

science Other reagents with same CAS 367966-45-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 359.53 g/mol
Formula C₁₇H₃₃NO₅Si
thermostat Physical Properties
Boiling Point 376.8±42.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.03±0.1 g/cm3(Predicted)
Storage room temperature

description Product Description

This compound is primarily utilized as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and biologically active molecules. Its structure, featuring both tert-butyl and tert-butyldimethylsilyl protecting groups, makes it valuable in multi-step synthetic processes where selective deprotection is required. It is often employed in the synthesis of complex molecules, such as natural products or drug candidates, where the pyrrolidine ring serves as a key structural motif. The compound's stereochemistry also plays a crucial role in the synthesis of chiral compounds, ensuring the desired enantiomeric purity in the final product. Its application is especially prominent in medicinal chemistry for the development of drugs targeting neurological disorders, cardiovascular diseases, and other therapeutic areas.

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Test Parameter Specification
Appearance Colorless Oil
Purity (%) 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿11,628.00
inventory 100mg
10-20 days ฿6,966.00

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(2S,4S)-1-Tert-Butyl 2-Methyl 4-((Tert-Butyldimethylsilyl)Oxy)Pyrrolidine-1,2-Dicarboxylate
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This compound is primarily utilized as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and biologically active molecules. Its structure, featuring both tert-butyl and tert-butyldimethylsilyl protecting groups, makes it valuable in multi-step synthetic processes where selective deprotection is required. It is often employed in the synthesis of complex molecules, such as natural products or drug candidates, where the pyrrolidine ring serves as a key structural motif. The compound's stereochemistry also plays a crucial role in the synthesis of chiral compounds, ensuring the desired enantiomeric purity in the final product. Its application is especially prominent in medicinal chemistry for the development of drugs targeting neurological disorders, cardiovascular diseases, and other therapeutic areas.
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