(2S,4R)-1-tert-butyl 2-methyl 4-(((benzyloxy)carbonyl)amino)pyrrolidine-1,2-dicarboxylate

95%

Reagent Code: #82868
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CAS Number 130047-39-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 378.42 g/mol
Formula C₁₉H₂₆N₂O₆
badge Registry Numbers
MDL Number MFCD18252794
thermostat Physical Properties
Boiling Point 504.5±50.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.22±0.1 g/cm3(Predicted)
Storage room temperature

description Product Description

This compound is primarily utilized in the synthesis of complex organic molecules, particularly in pharmaceutical research. It serves as a key intermediate in the development of peptidomimetics and other bioactive compounds. Its structure, featuring both tert-butyl and benzyloxycarbonyl protecting groups, makes it valuable for selective deprotection strategies during multi-step synthetic processes. The compound is often employed in the construction of pyrrolidine-based frameworks, which are common in drug molecules targeting various diseases. Its chiral centers also enable its use in asymmetric synthesis, contributing to the production of enantiomerically pure substances.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days €215.54
inventory 250mg
10-20 days €369.49
inventory 1g
10-20 days €738.98
(2S,4R)-1-tert-butyl 2-methyl 4-(((benzyloxy)carbonyl)amino)pyrrolidine-1,2-dicarboxylate
This compound is primarily utilized in the synthesis of complex organic molecules, particularly in pharmaceutical research. It serves as a key intermediate in the development of peptidomimetics and other bioactive compounds. Its structure, featuring both tert-butyl and benzyloxycarbonyl protecting groups, makes it valuable for selective deprotection strategies during multi-step synthetic processes. The compound is often employed in the construction of pyrrolidine-based frameworks, which are common in drug molecules targeting various diseases. Its chiral centers also enable its use in asymmetric synthesis, contributing to the production of enantiomerically pure substances.
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