cis-1-Boc-4-aminomethyl-3-hydroxypiperidine
97%
- Product Code: 123378
CAS:
219985-15-6
| Molecular Weight: | 230.3 g./mol | Molecular Formula: | C₁₁H₂₂N₂O₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD18791264 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, protected from light |
Product Description:
This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of active pharmaceutical ingredients (APIs). Its structure, featuring both a Boc-protected amine and a hydroxyl group, makes it a versatile building block in organic synthesis. It is often employed in the creation of complex molecules, including those used in the treatment of neurological disorders and other therapeutic areas. The Boc group provides protection for the amine during synthetic processes, allowing for selective reactions at other sites. Additionally, the hydroxyl group can be further modified or used as a handle for coupling reactions, enhancing its utility in medicinal chemistry. Its application is particularly significant in the design of piperidine-based compounds, which are common in drug discovery due to their biological activity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $411.63 |
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| 0.250 | 10-20 days | $687.69 |
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| 1.000 | 10-20 days | $1,717.64 |
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cis-1-Boc-4-aminomethyl-3-hydroxypiperidine
This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of active pharmaceutical ingredients (APIs). Its structure, featuring both a Boc-protected amine and a hydroxyl group, makes it a versatile building block in organic synthesis. It is often employed in the creation of complex molecules, including those used in the treatment of neurological disorders and other therapeutic areas. The Boc group provides protection for the amine during synthetic processes, allowing for selective reactions at other sites. Additionally, the hydroxyl group can be further modified or used as a handle for coupling reactions, enhancing its utility in medicinal chemistry. Its application is particularly significant in the design of piperidine-based compounds, which are common in drug discovery due to their biological activity.
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