(1-Benzylpiperazin-2-yl)methanol
97%
- Product Code: 36144
CAS:
476493-27-3
| Molecular Weight: | 206.2841 g./mol | Molecular Formula: | C₁₂H₁₈N₂O |
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| EC Number: | MDL Number: | MFCD16990491 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
(1-Benzylpiperazin-2-yl)methanol is a chemical compound with potential applications in the field of medicinal chemistry and drug development. It is often explored as a building block or intermediate in the synthesis of pharmacologically active molecules. The benzylpiperazine moiety is a common structural feature in compounds that interact with the central nervous system, making it relevant for the development of drugs targeting neurological disorders, such as antidepressants, antipsychotics, or anxiolytics. Additionally, the presence of the methanol group allows for further chemical modifications, enabling the creation of derivatives with enhanced biological activity or improved pharmacokinetic properties. Research into this compound may also extend to its potential use in studying receptor-ligand interactions, particularly in the context of serotonin or dopamine receptors, due to the structural similarity to known psychoactive substances.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿3,240.00 |
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(1-Benzylpiperazin-2-yl)methanol
(1-Benzylpiperazin-2-yl)methanol is a chemical compound with potential applications in the field of medicinal chemistry and drug development. It is often explored as a building block or intermediate in the synthesis of pharmacologically active molecules. The benzylpiperazine moiety is a common structural feature in compounds that interact with the central nervous system, making it relevant for the development of drugs targeting neurological disorders, such as antidepressants, antipsychotics, or anxiolytics. Additionally, the presence of the methanol group allows for further chemical modifications, enabling the creation of derivatives with enhanced biological activity or improved pharmacokinetic properties. Research into this compound may also extend to its potential use in studying receptor-ligand interactions, particularly in the context of serotonin or dopamine receptors, due to the structural similarity to known psychoactive substances.
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