Ethyl 1-Boc-3-methylpiperidine-3-carboxylate
≥95%
- Product Code: 76167
CAS:
278789-43-8
| Molecular Weight: | 271.35 g./mol | Molecular Formula: | C₁₄H₂₅NO₄ |
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| EC Number: | MDL Number: | MFCD11559117 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry |
Product Description:
Ethyl 1-Boc-3-methylpiperidine-3-carboxylate is primarily utilized in organic synthesis as a key intermediate for the development of more complex molecules. Its structure, featuring both a Boc (tert-butoxycarbonyl) protecting group and an ester functional group, makes it highly versatile in pharmaceutical research. It is commonly employed in the synthesis of piperidine derivatives, which are crucial building blocks for various bioactive compounds, including potential drugs targeting neurological disorders or other therapeutic areas. The Boc group allows for selective deprotection, enabling further functionalization of the molecule during multi-step synthetic processes. Additionally, its ester group can be hydrolyzed or transformed into other functional groups, enhancing its utility in medicinal chemistry and drug discovery.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | Ft34,714.18 |
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| 1.000 | 10-20 days | Ft65,743.61 |
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Ethyl 1-Boc-3-methylpiperidine-3-carboxylate
Ethyl 1-Boc-3-methylpiperidine-3-carboxylate is primarily utilized in organic synthesis as a key intermediate for the development of more complex molecules. Its structure, featuring both a Boc (tert-butoxycarbonyl) protecting group and an ester functional group, makes it highly versatile in pharmaceutical research. It is commonly employed in the synthesis of piperidine derivatives, which are crucial building blocks for various bioactive compounds, including potential drugs targeting neurological disorders or other therapeutic areas. The Boc group allows for selective deprotection, enabling further functionalization of the molecule during multi-step synthetic processes. Additionally, its ester group can be hydrolyzed or transformed into other functional groups, enhancing its utility in medicinal chemistry and drug discovery.
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