tert-Butyl 4-(4-amino-2-cyanophenyl)piperazine-1-carboxylate
97%
- Product Code: 113294
CAS:
288251-85-4
| Molecular Weight: | 302.37 g./mol | Molecular Formula: | C₁₆H₂₂N₄O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD23135819 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, protected from light, stored in an inert gas |
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.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,647.00 |
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| 0.250 | 10-20 days | ฿2,952.00 |
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tert-Butyl 4-(4-amino-2-cyanophenyl)piperazine-1-carboxylate
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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