S-(−)-1-Boc-3-aminopyrrolidine

98%

Reagent Code: #216603
label
Alias (s)-(-)-N-tert-butoxycarbonyl-3-aminopyrrolidine; (S)-1-Boc-3-aminopyrrolidine
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CAS Number 147081-44-5

science Other reagents with same CAS 147081-44-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 186.25 g/mol
Formula C₉H₁₈N₂O₂
badge Registry Numbers
MDL Number MFCD03419271
thermostat Physical Properties
Boiling Point 216-217 °C(lit.)
inventory_2 Storage & Handling
Density 1.067 g/mL at 25 °C(lit.)
Storage Room temperature

description Product Description

Used in pharmaceutical synthesis as a chiral building block for developing bioactive molecules, particularly in the production of protease inhibitors and antiviral agents. Its Boc-protected amine and pyrrolidine structure make it valuable for constructing complex drug scaffolds with high enantioselectivity. Commonly employed in asymmetric synthesis and medicinal chemistry research to introduce stereochemically defined nitrogen-containing rings.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿300.00
5g
10-20 days ฿1,090.00
25g
10-20 days ฿4,340.00
100g
10-20 days ฿16,200.00
S-(−)-1-Boc-3-aminopyrrolidine
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Used in pharmaceutical synthesis as a chiral building block for developing bioactive molecules, particularly in the production of protease inhibitors and antiviral agents. Its Boc-protected amine and pyrrolidine structure make it valuable for constructing complex drug scaffolds with high enantioselectivity. Commonly employed in asymmetric synthesis and medicinal chemistry research to introduce stereochemically defined nitrogen-containing rings.

Used in pharmaceutical synthesis as a chiral building block for developing bioactive molecules, particularly in the production of protease inhibitors and antiviral agents. Its Boc-protected amine and pyrrolidine structure make it valuable for constructing complex drug scaffolds with high enantioselectivity. Commonly employed in asymmetric synthesis and medicinal chemistry research to introduce stereochemically defined nitrogen-containing rings.

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