1-(2-Chlorobenzyl)piperidin-4-amine hydrochloride
95%
- Product Code: 39217
CAS:
1158219-47-6
| Molecular Weight: | 261.1907 g./mol | Molecular Formula: | C₁₂H₁₈Cl₂N₂ |
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| EC Number: | MDL Number: | MFCD09455668 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmacologically active molecules. It is often employed in the development of compounds targeting the central nervous system, particularly in the design of potential antipsychotic and antidepressant agents. The chlorobenzyl and piperidine moieties in its structure make it a versatile building block for creating ligands that interact with neurotransmitter receptors, such as dopamine and serotonin receptors. Additionally, it is explored in research for its potential role in modulating histamine receptors, which could lead to applications in treating allergic conditions or sleep disorders. Its hydrochloride form enhances solubility, making it more suitable for use in experimental formulations and drug delivery systems.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿4,482.00 |
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1-(2-Chlorobenzyl)piperidin-4-amine hydrochloride
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmacologically active molecules. It is often employed in the development of compounds targeting the central nervous system, particularly in the design of potential antipsychotic and antidepressant agents. The chlorobenzyl and piperidine moieties in its structure make it a versatile building block for creating ligands that interact with neurotransmitter receptors, such as dopamine and serotonin receptors. Additionally, it is explored in research for its potential role in modulating histamine receptors, which could lead to applications in treating allergic conditions or sleep disorders. Its hydrochloride form enhances solubility, making it more suitable for use in experimental formulations and drug delivery systems.
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