tert-Butyl 4-(3-nitropyridin-2-yl)piperazine-1-carboxylate

95%

Reagent Code: #46236
label
Alias 1-Boc-4-(3-nitropyridin-2-yl)piperazine
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CAS Number 153473-24-6

science Other reagents with same CAS 153473-24-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 308.33 g/mol
Formula C₁₄H₂₀N₄O₄
badge Registry Numbers
MDL Number MFCD09028514
thermostat Physical Properties
Boiling Point 447.8°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in pharmaceutical research and development as an intermediate in the synthesis of biologically active molecules. Its structure, featuring both a piperazine ring and a nitropyridine moiety, makes it valuable for constructing compounds with potential therapeutic applications, particularly in the fields of central nervous system (CNS) disorders and oncology. Researchers often employ it to create derivatives that can interact with specific receptors or enzymes, aiding in the discovery of new drugs. Additionally, its tert-butyl group provides stability and facilitates further chemical modifications, making it a versatile building block in medicinal chemistry.

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Test Parameter Specification
Purity 94.5-100
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿9,198.00
inventory 250mg
10-20 days ฿3,798.00

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tert-Butyl 4-(3-nitropyridin-2-yl)piperazine-1-carboxylate
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This compound is primarily utilized in pharmaceutical research and development as an intermediate in the synthesis of biologically active molecules. Its structure, featuring both a piperazine ring and a nitropyridine moiety, makes it valuable for constructing compounds with potential therapeutic applications, particularly in the fields of central nervous system (CNS) disorders and oncology. Researchers often employ it to create derivatives that can interact with specific receptors or enzymes, aiding in the discovery of new drugs. Additionally, its tert-butyl group provides stability and facilitates further chemical modifications, making it a versatile building block in medicinal chemistry.
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