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

95%

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

science Other reagents with same CAS 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.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿8,190.00
250mg
10-20 days ฿14,040.00
1g
10-20 days ฿28,080.00
(2S,4R)-1-tert-butyl 2-methyl 4-(((benzyloxy)carbonyl)amino)pyrrolidine-1,2-dicarboxylate
No image available

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 dru

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.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...