(R)-tert-Butyl 3-(cyclopropylamino)pyrrolidine-1-carboxylate

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Reagent Code: #231152
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CAS Number 1289584-93-5

science Other reagents with same CAS 1289584-93-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 226.315 g/mol
Formula C₁₂H₂₂N₂O₂
badge Registry Numbers
MDL Number MFCD18837099
thermostat Physical Properties
Boiling Point 311.8±35.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.08 g/cm3
Storage 2-8°C

description Product Description

Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and antiviral agents. Its structure supports the formation of stereoselective bonds, making it valuable in asymmetric synthesis. Commonly employed in the preparation of active pharmaceutical ingredients (APIs) where the (R)-enantiomer provides optimal biological activity. Also utilized in medicinal chemistry research for constructing nitrogen-containing heterocycles with improved metabolic stability and binding affinity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿19,750.00
inventory 1g
10-20 days ฿59,360.00
(R)-tert-Butyl 3-(cyclopropylamino)pyrrolidine-1-carboxylate
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Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and antiviral agents. Its structure supports the formation of stereoselective bonds, making it valuable in asymmetric synthesis. Commonly employed in the preparation of active pharmaceutical ingredients (APIs) where the (R)-enantiomer provides optimal biological activity. Also utilized in medicinal chemistry research for constructing nitrogen-containing heterocycles with improved

Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and antiviral agents. Its structure supports the formation of stereoselective bonds, making it valuable in asymmetric synthesis. Commonly employed in the preparation of active pharmaceutical ingredients (APIs) where the (R)-enantiomer provides optimal biological activity. Also utilized in medicinal chemistry research for constructing nitrogen-containing heterocycles with improved metabolic stability and binding affinity.

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