Benzyl 4-((3-bromophenoxy)methyl)piperidine-1-carboxylate
97%
- Product Code: 46016
CAS:
2061979-51-7
| Molecular Weight: | 404.30 g./mol | Molecular Formula: | C₂₀H₂₂BrNO₃ |
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| EC Number: | MDL Number: | MFCD30609583 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, dry and sealed |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as an intermediate in the synthesis of more complex molecules, particularly those targeting neurological disorders. Its structure, featuring a piperidine ring and a bromophenoxy group, makes it a valuable building block for developing compounds with potential activity at neurotransmitter receptors. Researchers often explore its derivatives for their ability to modulate receptors such as serotonin or dopamine, which are critical in treating conditions like depression, anxiety, and Parkinson's disease. Additionally, the bromine atom in its structure allows for further functionalization through various coupling reactions, enabling the creation of diverse pharmacologically active compounds. Its application is largely confined to laboratory research and drug development processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | €19.94 |
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| 0.250 | 10-20 days | €33.48 |
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| 1.000 | 10-20 days | €89.99 |
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Benzyl 4-((3-bromophenoxy)methyl)piperidine-1-carboxylate
This compound is primarily utilized in the field of medicinal chemistry as an intermediate in the synthesis of more complex molecules, particularly those targeting neurological disorders. Its structure, featuring a piperidine ring and a bromophenoxy group, makes it a valuable building block for developing compounds with potential activity at neurotransmitter receptors. Researchers often explore its derivatives for their ability to modulate receptors such as serotonin or dopamine, which are critical in treating conditions like depression, anxiety, and Parkinson's disease. Additionally, the bromine atom in its structure allows for further functionalization through various coupling reactions, enabling the creation of diverse pharmacologically active compounds. Its application is largely confined to laboratory research and drug development processes.
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