1-(tert-butyl)-3,4-dimethylcis-pyrrolidine-1,3,4-tricarboxylate

98%

Reagent Code: #64499

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 287.31 g/mol
Formula C₁₃H₂₁NO₆
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

This compound is primarily utilized in organic synthesis as a versatile intermediate for the development of complex molecules. Its structure, featuring multiple carboxylate groups and a tert-butyl moiety, makes it suitable for constructing pharmacologically active compounds, particularly in the synthesis of chiral pyrrolidine derivatives. These derivatives are often key components in the production of drugs targeting neurological and cardiovascular disorders. Additionally, the steric hindrance provided by the tert-butyl group enhances selectivity in chemical reactions, making it valuable in asymmetric synthesis. It is also employed in the preparation of ligands for catalytic systems, contributing to advancements in stereoselective transformations.

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Test Parameter Specification
Appearance White Solid
Purity 97.5-100
Infrared Spectrum Conforms to Structure

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Size Availability Unit Price Quantity
inventory 10g
10-20 days ฿64,000.00
inventory 250mg
10-20 days ฿4,920.00
inventory 5g
10-20 days ฿38,000.00
inventory 1g
10-20 days ฿12,800.00

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1-(tert-butyl)-3,4-dimethylcis-pyrrolidine-1,3,4-tricarboxylate
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This compound is primarily utilized in organic synthesis as a versatile intermediate for the development of complex molecules. Its structure, featuring multiple carboxylate groups and a tert-butyl moiety, makes it suitable for constructing pharmacologically active compounds, particularly in the synthesis of chiral pyrrolidine derivatives. These derivatives are often key components in the production of drugs targeting neurological and cardiovascular disorders. Additionally, the steric hindrance provided by t
This compound is primarily utilized in organic synthesis as a versatile intermediate for the development of complex molecules. Its structure, featuring multiple carboxylate groups and a tert-butyl moiety, makes it suitable for constructing pharmacologically active compounds, particularly in the synthesis of chiral pyrrolidine derivatives. These derivatives are often key components in the production of drugs targeting neurological and cardiovascular disorders. Additionally, the steric hindrance provided by the tert-butyl group enhances selectivity in chemical reactions, making it valuable in asymmetric synthesis. It is also employed in the preparation of ligands for catalytic systems, contributing to advancements in stereoselective transformations.
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