Methyl N-Boc-4-(trifluoroacetylamino)piperidine-4-carboxylate
≥97%
- Product Code: 76498
CAS:
1375064-57-5
| Molecular Weight: | 354.32 g./mol | Molecular Formula: | C₁₄H₂₁F₃N₂O₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD22192346 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This compound is primarily utilized in organic synthesis as a versatile intermediate, particularly in the development of pharmaceuticals and bioactive molecules. Its structure, featuring both Boc and trifluoroacetyl protecting groups, makes it valuable for selective deprotection strategies, enabling the construction of complex piperidine-based compounds. It is often employed in the synthesis of potential drug candidates, especially those targeting neurological disorders or as building blocks for peptidomimetics. The trifluoroacetyl group enhances reactivity in certain transformations, while the Boc group provides stability during synthetic processes. Its applications extend to medicinal chemistry research, where it aids in the exploration of new therapeutic agents with improved efficacy and selectivity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿10,791.00 |
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| 5.000 | 10-20 days | ฿36,711.00 |
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Methyl N-Boc-4-(trifluoroacetylamino)piperidine-4-carboxylate
This compound is primarily utilized in organic synthesis as a versatile intermediate, particularly in the development of pharmaceuticals and bioactive molecules. Its structure, featuring both Boc and trifluoroacetyl protecting groups, makes it valuable for selective deprotection strategies, enabling the construction of complex piperidine-based compounds. It is often employed in the synthesis of potential drug candidates, especially those targeting neurological disorders or as building blocks for peptidomimetics. The trifluoroacetyl group enhances reactivity in certain transformations, while the Boc group provides stability during synthetic processes. Its applications extend to medicinal chemistry research, where it aids in the exploration of new therapeutic agents with improved efficacy and selectivity.
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