tert-Butyl 4-((4-bromobenzyl)oxy)piperidine-1-carboxylate
97%
- Product Code: 86080
CAS:
930111-10-7
| Molecular Weight: | 370.28 g./mol | Molecular Formula: | C₁₇H₂₄BrNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09879975 | |
| Melting Point: | Boiling Point: | 429.4°C at 760 mmHg | |
| Density: | 1.31g/cm3 | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This compound is primarily used in organic synthesis as an intermediate in the development of pharmaceuticals. Its structure, featuring a piperidine ring and a bromobenzyl group, makes it valuable for constructing more complex molecules, particularly in the synthesis of bioactive compounds. It is often employed in medicinal chemistry research to create potential drug candidates, especially those targeting neurological or psychiatric disorders. The presence of the bromine atom allows for further functionalization through cross-coupling reactions, enabling the introduction of diverse chemical groups. Additionally, the tert-butyloxycarbonyl (Boc) protecting group ensures stability during synthetic processes, making it a versatile building block in multi-step organic reactions.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | Ft55,368.14 |
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| 0.250 | 10-20 days | Ft88,239.94 |
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| 1.000 | 10-20 days | Ft221,666.50 |
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tert-Butyl 4-((4-bromobenzyl)oxy)piperidine-1-carboxylate
This compound is primarily used in organic synthesis as an intermediate in the development of pharmaceuticals. Its structure, featuring a piperidine ring and a bromobenzyl group, makes it valuable for constructing more complex molecules, particularly in the synthesis of bioactive compounds. It is often employed in medicinal chemistry research to create potential drug candidates, especially those targeting neurological or psychiatric disorders. The presence of the bromine atom allows for further functionalization through cross-coupling reactions, enabling the introduction of diverse chemical groups. Additionally, the tert-butyloxycarbonyl (Boc) protecting group ensures stability during synthetic processes, making it a versatile building block in multi-step organic reactions.
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