Methyl 1-Boc-4-methylpiperidine-4-carboxylate
≥97%
- Product Code: 76190
CAS:
724790-59-4
| Molecular Weight: | 257.33 g./mol | Molecular Formula: | C₁₃H₂₃NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08062512 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This compound is primarily used in organic synthesis as an intermediate in the production of pharmaceuticals and bioactive molecules. Its structure, featuring a Boc-protected amine and a carboxylate ester, makes it a versatile building block for constructing complex molecules, particularly in drug discovery and development. It is often employed in the synthesis of piperidine derivatives, which are common structural motifs in many drugs, including those targeting neurological disorders, cardiovascular diseases, and cancer. The Boc group provides protection for the amine during reactions, allowing selective modifications to other parts of the molecule. Additionally, the ester group can be hydrolyzed or further transformed into other functional groups, enhancing its utility in multi-step synthetic routes. Its application is particularly valuable in medicinal chemistry for creating libraries of compounds for biological screening.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿2,556.00 |
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| 5.000 | 10-20 days | ฿8,100.00 |
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Methyl 1-Boc-4-methylpiperidine-4-carboxylate
This compound is primarily used in organic synthesis as an intermediate in the production of pharmaceuticals and bioactive molecules. Its structure, featuring a Boc-protected amine and a carboxylate ester, makes it a versatile building block for constructing complex molecules, particularly in drug discovery and development. It is often employed in the synthesis of piperidine derivatives, which are common structural motifs in many drugs, including those targeting neurological disorders, cardiovascular diseases, and cancer. The Boc group provides protection for the amine during reactions, allowing selective modifications to other parts of the molecule. Additionally, the ester group can be hydrolyzed or further transformed into other functional groups, enhancing its utility in multi-step synthetic routes. Its application is particularly valuable in medicinal chemistry for creating libraries of compounds for biological screening.
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