R-()-1-Boc-3-aminopyrrolidine

Standard for GC, ≥99.9%(GC)

Reagent Code: #228571
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CAS Number 147081-49-0

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 186.25 g/mol
Formula C₉H₁₈N₂O₂
badge Registry Numbers
MDL Number MFCD03419272
thermostat Physical Properties
Melting Point 243-244 °C
Boiling Point 243-244 °C
inventory_2 Storage & Handling
Density 1.098 g/mL at 25 °C (lit.)
Storage Room temperature

description Product Description

Used in pharmaceutical synthesis as a chiral building block for developing active pharmaceutical ingredients (APIs), particularly in the production of protease inhibitors and other biologically active molecules. Its protected amine and pyrrolidine structure make it valuable in asymmetric synthesis and drug development where stereochemistry is critical. Commonly employed in the preparation of antiviral and anticancer agents due to its ability to mimic natural amino acid frameworks and enhance binding selectivity.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿3,000.00
R-()-1-Boc-3-aminopyrrolidine
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Used in pharmaceutical synthesis as a chiral building block for developing active pharmaceutical ingredients (APIs), particularly in the production of protease inhibitors and other biologically active molecules. Its protected amine and pyrrolidine structure make it valuable in asymmetric synthesis and drug development where stereochemistry is critical. Commonly employed in the preparation of antiviral and anticancer agents due to its ability to mimic natural amino acid frameworks and enhance binding sele

Used in pharmaceutical synthesis as a chiral building block for developing active pharmaceutical ingredients (APIs), particularly in the production of protease inhibitors and other biologically active molecules. Its protected amine and pyrrolidine structure make it valuable in asymmetric synthesis and drug development where stereochemistry is critical. Commonly employed in the preparation of antiviral and anticancer agents due to its ability to mimic natural amino acid frameworks and enhance binding selectivity.

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