tert-Butyl 4-((2-hydroxyethoxy)methyl)piperidine-1-carboxylate
97%
- Product Code: 85390
CAS:
1260099-72-6
| Molecular Weight: | 259.34 g./mol | Molecular Formula: | C₁₃H₂₅NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD21092246 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This chemical is primarily used in organic synthesis as an intermediate for the development of more complex compounds. Its structure, featuring both a piperidine ring and a protected hydroxyl group, makes it valuable in the preparation of pharmaceuticals, particularly in the synthesis of active pharmaceutical ingredients (APIs). It is often utilized in the production of drugs targeting the central nervous system, such as analgesics or anti-inflammatory agents, due to the piperidine moiety's role in interacting with biological receptors. Additionally, the tert-butyl group provides stability during synthetic processes, allowing for selective reactions and easier purification. Its application extends to the field of medicinal chemistry, where it serves as a building block for designing molecules with potential therapeutic effects.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿14,931.00 |
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| 0.250 | 10-20 days | ฿26,118.00 |
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| 1.000 | 10-20 days | ฿65,295.00 |
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tert-Butyl 4-((2-hydroxyethoxy)methyl)piperidine-1-carboxylate
This chemical is primarily used in organic synthesis as an intermediate for the development of more complex compounds. Its structure, featuring both a piperidine ring and a protected hydroxyl group, makes it valuable in the preparation of pharmaceuticals, particularly in the synthesis of active pharmaceutical ingredients (APIs). It is often utilized in the production of drugs targeting the central nervous system, such as analgesics or anti-inflammatory agents, due to the piperidine moiety's role in interacting with biological receptors. Additionally, the tert-butyl group provides stability during synthetic processes, allowing for selective reactions and easier purification. Its application extends to the field of medicinal chemistry, where it serves as a building block for designing molecules with potential therapeutic effects.
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