(2-Amino-4-bromophenyl) [4-(methylsulfonyl) - 1-piperazinyl] ketone
95%
- Product Code: 36366
CAS:
1539817-33-8
| Molecular Weight: | 362.24274 g./mol | Molecular Formula: | C₁₂H₁₆BrN₃O₃S |
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| Density: | Storage Condition: | 2-8℃ |
Product Description:
(2-Amino-4-bromophenyl) [4-(methylsulfonyl)-1-piperazinyl] ketone is primarily utilized in pharmaceutical research and development, particularly in the synthesis of novel compounds with potential therapeutic applications. Its structure, featuring both a bromophenyl group and a piperazinyl moiety, makes it a valuable intermediate in the design of molecules targeting central nervous system disorders. Researchers often explore its use in creating ligands for receptors involved in neurological pathways, such as dopamine or serotonin receptors, due to its ability to modulate receptor activity. Additionally, its sulfonyl group enhances its potential as a precursor in the development of anti-inflammatory or anticancer agents, as sulfonamides are known for their biological activity. The compound's versatility also extends to organic synthesis, where it serves as a building block for more complex chemical structures in medicinal chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿11,592.00 |
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| 1.000 | 10-20 days | ฿27,792.00 |
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| 5.000 | 10-20 days | ฿72,792.00 |
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(2-Amino-4-bromophenyl) [4-(methylsulfonyl) - 1-piperazinyl] ketone
(2-Amino-4-bromophenyl) [4-(methylsulfonyl)-1-piperazinyl] ketone is primarily utilized in pharmaceutical research and development, particularly in the synthesis of novel compounds with potential therapeutic applications. Its structure, featuring both a bromophenyl group and a piperazinyl moiety, makes it a valuable intermediate in the design of molecules targeting central nervous system disorders. Researchers often explore its use in creating ligands for receptors involved in neurological pathways, such as dopamine or serotonin receptors, due to its ability to modulate receptor activity. Additionally, its sulfonyl group enhances its potential as a precursor in the development of anti-inflammatory or anticancer agents, as sulfonamides are known for their biological activity. The compound's versatility also extends to organic synthesis, where it serves as a building block for more complex chemical structures in medicinal chemistry.
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