1-(6-Bromo-3-pyridyl)-4-methylpiperazine
95%
- Product Code: 39524
CAS:
879488-53-6
| Molecular Weight: | 256.1400 g./mol | Molecular Formula: | C₁₀H₁₄BrN₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD14702603 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting neurological and psychiatric disorders. Its structure, featuring a pyridine ring and a piperazine moiety, makes it a valuable building block for developing compounds that interact with neurotransmitter receptors, such as dopamine or serotonin receptors. Researchers often employ it in the design and optimization of potential drug candidates for conditions like schizophrenia, depression, and anxiety. Additionally, its bromo substituent allows for further functionalization through cross-coupling reactions, enabling the creation of diverse derivatives for structure-activity relationship studies.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿4,050.00 |
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1-(6-Bromo-3-pyridyl)-4-methylpiperazine
This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting neurological and psychiatric disorders. Its structure, featuring a pyridine ring and a piperazine moiety, makes it a valuable building block for developing compounds that interact with neurotransmitter receptors, such as dopamine or serotonin receptors. Researchers often employ it in the design and optimization of potential drug candidates for conditions like schizophrenia, depression, and anxiety. Additionally, its bromo substituent allows for further functionalization through cross-coupling reactions, enabling the creation of diverse derivatives for structure-activity relationship studies.
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