(R)-2-Benzyl 1-tert-butyl 5-oxopyrrolidine-1,2-dicarboxylate

≥95%

Reagent Code: #37751
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CAS Number 400626-71-3

science Other reagents with same CAS 400626-71-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 319.35 g/mol
Formula C₁₇H₂₁NO₅
badge Registry Numbers
MDL Number MFCD14635665
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This compound is primarily utilized in organic synthesis as a chiral building block for the preparation of more complex molecules, particularly in pharmaceutical research. Its structure, featuring both benzyl and tert-butyl ester groups, makes it valuable for selective deprotection strategies during multi-step syntheses. It is often employed in the development of peptidomimetics and other bioactive compounds, where the stereochemistry at the chiral center plays a critical role in biological activity. Additionally, its pyrrolidine core is useful in constructing heterocyclic frameworks, which are common in drug discovery. The compound’s stability and reactivity also make it suitable for use in asymmetric synthesis and catalysis studies.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿4,518.00
inventory 250mg
10-20 days ฿1,503.00
inventory 100mg
10-20 days ฿900.00

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(R)-2-Benzyl 1-tert-butyl 5-oxopyrrolidine-1,2-dicarboxylate
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This compound is primarily utilized in organic synthesis as a chiral building block for the preparation of more complex molecules, particularly in pharmaceutical research. Its structure, featuring both benzyl and tert-butyl ester groups, makes it valuable for selective deprotection strategies during multi-step syntheses. It is often employed in the development of peptidomimetics and other bioactive compounds, where the stereochemistry at the chiral center plays a critical role in biological activity. Add

This compound is primarily utilized in organic synthesis as a chiral building block for the preparation of more complex molecules, particularly in pharmaceutical research. Its structure, featuring both benzyl and tert-butyl ester groups, makes it valuable for selective deprotection strategies during multi-step syntheses. It is often employed in the development of peptidomimetics and other bioactive compounds, where the stereochemistry at the chiral center plays a critical role in biological activity. Additionally, its pyrrolidine core is useful in constructing heterocyclic frameworks, which are common in drug discovery. The compound’s stability and reactivity also make it suitable for use in asymmetric synthesis and catalysis studies.

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