(3aS,6aS)-rel-tert-Butyl hexahydropyrrolo[3,4-b]pyrrole-1(2H)-carboxylate

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Reagent Code: #70898
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CAS Number 1018443-32-7

science Other reagents with same CAS 1018443-32-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 212.29 g/mol
Formula C₁₁H₂₀N₂O₂
badge Registry Numbers
MDL Number MFCD12198661
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of complex molecules, particularly in pharmaceutical research. Its structure is valuable for constructing pyrrolidine-based frameworks, which are commonly found in bioactive compounds. The tert-butyl group enhances stability and facilitates selective reactions, making it useful in the development of drug candidates targeting various diseases. Additionally, its stereochemistry allows for the creation of chiral molecules, which are critical in designing enantioselective drugs. Researchers also employ it in the synthesis of natural products and heterocyclic compounds, leveraging its versatility in multi-step synthetic routes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,300.00
inventory 250mg
10-20 days ฿10,647.00
inventory 1g
10-20 days ฿24,885.00

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(3aS,6aS)-rel-tert-Butyl hexahydropyrrolo[3,4-b]pyrrole-1(2H)-carboxylate
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This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of complex molecules, particularly in pharmaceutical research. Its structure is valuable for constructing pyrrolidine-based frameworks, which are commonly found in bioactive compounds. The tert-butyl group enhances stability and facilitates selective reactions, making it useful in the development of drug candidates targeting various diseases. Additionally, its stereochemistry allows for the creation of chiral molecules, which are critical in designing enantioselective drugs. Researchers also employ it in the synthesis of natural products and heterocyclic compounds, leveraging its versatility in multi-step synthetic routes.
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