tert-Butyl 3-bromopyrrolidine-1-carboxylate

98%

Reagent Code: #145171
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CAS Number 939793-16-5

science Other reagents with same CAS 939793-16-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 250.13 g/mol
Formula C₉H₁₆BrNO₂
thermostat Physical Properties
Melting Point 47-52°C
Boiling Point 277.5±33.0°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in pharmaceutical synthesis, particularly in the development of active pharmaceutical ingredients (APIs) where the pyrrolidine ring serves as a structural scaffold. The bromine atom allows for further functionalization through cross-coupling reactions, making it valuable in medicinal chemistry for building complex molecules. The tert-butoxycarbonyl (Boc) protecting group ensures selective reactivity by shielding the nitrogen during multi-step syntheses. Commonly employed in the preparation of protease inhibitors, receptor agonists, and other bioactive compounds.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿400.00
inventory 1g
10-20 days ฿780.00
inventory 5g
10-20 days ฿2,720.00
inventory 100g
10-20 days ฿53,280.00
inventory 25g
10-20 days ฿13,350.00
tert-Butyl 3-bromopyrrolidine-1-carboxylate
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Used as an intermediate in pharmaceutical synthesis, particularly in the development of active pharmaceutical ingredients (APIs) where the pyrrolidine ring serves as a structural scaffold. The bromine atom allows for further functionalization through cross-coupling reactions, making it valuable in medicinal chemistry for building complex molecules. The tert-butoxycarbonyl (Boc) protecting group ensures selective reactivity by shielding the nitrogen during multi-step syntheses. Commonly employed in the pr

Used as an intermediate in pharmaceutical synthesis, particularly in the development of active pharmaceutical ingredients (APIs) where the pyrrolidine ring serves as a structural scaffold. The bromine atom allows for further functionalization through cross-coupling reactions, making it valuable in medicinal chemistry for building complex molecules. The tert-butoxycarbonyl (Boc) protecting group ensures selective reactivity by shielding the nitrogen during multi-step syntheses. Commonly employed in the preparation of protease inhibitors, receptor agonists, and other bioactive compounds.

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