1-N-Boc-3-(4-Bromophenoxy)pyrrolidine

97%

Reagent Code: #114560
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CAS Number 1159825-42-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 342.23 g/mol
Formula C₁₅H₂₀BrNO₃
badge Registry Numbers
MDL Number MFCD12068410
thermostat Physical Properties
Boiling Point 403.6±35.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This chemical is widely used in organic synthesis, particularly in the development of pharmaceuticals and bioactive compounds. It serves as a key intermediate in the preparation of complex molecules, especially those involving pyrrolidine derivatives. The Boc (tert-butoxycarbonyl) group provides protection for the amine functionality during multi-step synthetic processes, allowing for selective reactions at other sites of the molecule. The presence of the 4-bromophenoxy moiety makes it valuable for further functionalization through cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, which are essential in constructing advanced drug candidates. Its application is particularly significant in the synthesis of compounds targeting neurological disorders, cancer, and other therapeutic areas.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,278.00
inventory 250mg
10-20 days ฿2,025.00
inventory 1g
10-20 days ฿5,193.00
1-N-Boc-3-(4-Bromophenoxy)pyrrolidine
This chemical is widely used in organic synthesis, particularly in the development of pharmaceuticals and bioactive compounds. It serves as a key intermediate in the preparation of complex molecules, especially those involving pyrrolidine derivatives. The Boc (tert-butoxycarbonyl) group provides protection for the amine functionality during multi-step synthetic processes, allowing for selective reactions at other sites of the molecule. The presence of the 4-bromophenoxy moiety makes it valuable for further functionalization through cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, which are essential in constructing advanced drug candidates. Its application is particularly significant in the synthesis of compounds targeting neurological disorders, cancer, and other therapeutic areas.
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