tert-butyl 4-(4-bromophenethyl)piperazine-1-carboxylate

95%

Reagent Code: #64558
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CAS Number 1007209-94-0

science Other reagents with same CAS 1007209-94-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 369.3 g/mol
Formula C₁₇H₂₅BrN₂O₂
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

This compound is primarily utilized in organic synthesis and pharmaceutical research as an intermediate. It plays a crucial role in the development of bioactive molecules, particularly in the synthesis of piperazine derivatives, which are often explored for their potential therapeutic applications. The presence of the bromophenethyl group makes it a valuable building block for constructing more complex structures, especially in drug discovery programs targeting neurological disorders or other conditions where piperazine-based compounds show promise. Its tert-butyl carboxylate group provides stability and ease of handling during chemical transformations, making it a preferred choice in multi-step synthetic routes.

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Test Parameter Specification
Appearance White solid
Purity 94.5-100
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,860.00
inventory 1g
10-20 days ฿8,820.00
inventory 10g
10-20 days ฿66,000.00
inventory 100mg
10-20 days ฿3,600.00

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tert-butyl 4-(4-bromophenethyl)piperazine-1-carboxylate
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This compound is primarily utilized in organic synthesis and pharmaceutical research as an intermediate. It plays a crucial role in the development of bioactive molecules, particularly in the synthesis of piperazine derivatives, which are often explored for their potential therapeutic applications. The presence of the bromophenethyl group makes it a valuable building block for constructing more complex structures, especially in drug discovery programs targeting neurological disorders or other conditions where piperazine-based compounds show promise. Its tert-butyl carboxylate group provides stability and ease of handling during chemical transformations, making it a preferred choice in multi-step synthetic routes.
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