tert-Butyl 4-(4-amino-2-cyanophenyl)piperazine-1-carboxylate

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Reagent Code: #113294
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CAS Number 288251-85-4

science Other reagents with same CAS 288251-85-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 302.37 g/mol
Formula C₁₆H₂₂N₄O₂
badge Registry Numbers
MDL Number MFCD23135819
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in an inert gas

description Product Description

This chemical is primarily utilized in pharmaceutical research and development, particularly in the synthesis of novel compounds with potential therapeutic applications. Its structure, featuring both a piperazine ring and a cyano group, makes it a valuable intermediate in the creation of molecules targeting various biological pathways. It is often employed in the design of drugs that interact with central nervous system receptors, such as serotonin or dopamine receptors, due to the piperazine moiety's ability to enhance binding affinity. Additionally, the presence of the cyano group allows for further chemical modifications, enabling researchers to explore a wide range of derivatives with diverse pharmacological properties. Its application extends to the development of potential treatments for psychiatric disorders, neurodegenerative diseases, and other conditions where modulation of neurotransmitter systems is beneficial.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,952.00
inventory 100mg
10-20 days ฿1,647.00

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tert-Butyl 4-(4-amino-2-cyanophenyl)piperazine-1-carboxylate
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This chemical is primarily utilized in pharmaceutical research and development, particularly in the synthesis of novel compounds with potential therapeutic applications. Its structure, featuring both a piperazine ring and a cyano group, makes it a valuable intermediate in the creation of molecules targeting various biological pathways. It is often employed in the design of drugs that interact with central nervous system receptors, such as serotonin or dopamine receptors, due to the piperazine moiety's ability to enhance binding affinity. Additionally, the presence of the cyano group allows for further chemical modifications, enabling researchers to explore a wide range of derivatives with diverse pharmacological properties. Its application extends to the development of potential treatments for psychiatric disorders, neurodegenerative diseases, and other conditions where modulation of neurotransmitter systems is beneficial.
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