benzyl 4-((tert-butoxycarbonyl)amino)-4-methylpiperidine-1-carboxylate
95%
- Product Code: 83763
CAS:
169750-60-1
| Molecular Weight: | 348.44 g./mol | Molecular Formula: | C₁₉H₂₈N₂O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD23099450 | |
| Melting Point: | Boiling Point: | 473.1±44.0 °C(Predicted) | |
| Density: | 1.14±0.1 g/cm3(Predicted) | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceuticals. It serves as a key intermediate in the synthesis of complex molecules, especially those involving piperidine derivatives. Its structure, featuring both a tert-butoxycarbonyl (Boc) protecting group and a benzyl ester, makes it valuable in peptide and medicinal chemistry. The Boc group is commonly used to protect amines during multi-step synthetic processes, while the benzyl ester can be selectively removed under mild conditions. This chemical is often employed in the preparation of biologically active compounds, including potential drug candidates targeting neurological disorders, due to the piperidine moiety’s presence in many pharmacologically relevant structures. Its application extends to the synthesis of inhibitors, receptor modulators, and other therapeutic agents.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿5,265.00 |
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| 1.000 | 10-20 days | ฿10,530.00 |
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| 5.000 | 10-20 days | ฿31,590.00 |
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benzyl 4-((tert-butoxycarbonyl)amino)-4-methylpiperidine-1-carboxylate
This compound is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceuticals. It serves as a key intermediate in the synthesis of complex molecules, especially those involving piperidine derivatives. Its structure, featuring both a tert-butoxycarbonyl (Boc) protecting group and a benzyl ester, makes it valuable in peptide and medicinal chemistry. The Boc group is commonly used to protect amines during multi-step synthetic processes, while the benzyl ester can be selectively removed under mild conditions. This chemical is often employed in the preparation of biologically active compounds, including potential drug candidates targeting neurological disorders, due to the piperidine moiety’s presence in many pharmacologically relevant structures. Its application extends to the synthesis of inhibitors, receptor modulators, and other therapeutic agents.
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