Methyl 2-(1,4-dibenzylpiperazin-2-yl)acetate
97%
- Product Code: 41202
CAS:
183742-32-7
| Molecular Weight: | 338.4434 g./mol | Molecular Formula: | C₂₁H₂₆N₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00674203 | |
| Melting Point: | Boiling Point: | 441.296 °C at 760 mmHg | |
| Density: | 1.118g/cm3 | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as an intermediate in the synthesis of various pharmacologically active molecules. Its structure, featuring a piperazine ring and benzyl groups, makes it a versatile building block for developing compounds targeting the central nervous system. It is particularly relevant in the design of potential antipsychotic and antidepressant agents, as piperazine derivatives are known to interact with neurotransmitter receptors. Additionally, it may be employed in research focused on modulating serotonin and dopamine pathways, contributing to the development of treatments for neurological and psychiatric disorders. Its ester functional group also allows for further chemical modifications, enabling the creation of diverse derivatives for drug discovery and optimization.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | £289.66 |
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Methyl 2-(1,4-dibenzylpiperazin-2-yl)acetate
This compound is primarily utilized in the field of medicinal chemistry as an intermediate in the synthesis of various pharmacologically active molecules. Its structure, featuring a piperazine ring and benzyl groups, makes it a versatile building block for developing compounds targeting the central nervous system. It is particularly relevant in the design of potential antipsychotic and antidepressant agents, as piperazine derivatives are known to interact with neurotransmitter receptors. Additionally, it may be employed in research focused on modulating serotonin and dopamine pathways, contributing to the development of treatments for neurological and psychiatric disorders. Its ester functional group also allows for further chemical modifications, enabling the creation of diverse derivatives for drug discovery and optimization.
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