tert-Butyl 4-(2-ethoxy-1,1-difluoro-2-oxoethyl)piperidine-1-carboxylate
97%
- Product Code: 124237
CAS:
1258639-00-7
| Molecular Weight: | 307.33 g./mol | Molecular Formula: | C₁₄H₂₃F₂NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD18433766 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This compound is primarily utilized in organic synthesis as a versatile intermediate for the development of more complex molecules. Its structure, featuring a piperidine ring and difluoroethoxy moiety, makes it valuable in medicinal chemistry for the design of potential pharmaceutical agents. It is often employed in the synthesis of compounds targeting neurological disorders, as the piperidine scaffold is a common feature in drugs affecting the central nervous system. Additionally, the difluoro group can enhance the metabolic stability and bioavailability of the resulting molecules. Researchers also explore its use in agrochemical research for creating novel pesticides or herbicides, leveraging its unique chemical properties to improve efficacy and selectivity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿8,739.00 |
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| 0.250 | 10-20 days | ฿14,850.00 |
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| 1.000 | 10-20 days | ฿40,077.00 |
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tert-Butyl 4-(2-ethoxy-1,1-difluoro-2-oxoethyl)piperidine-1-carboxylate
This compound is primarily utilized in organic synthesis as a versatile intermediate for the development of more complex molecules. Its structure, featuring a piperidine ring and difluoroethoxy moiety, makes it valuable in medicinal chemistry for the design of potential pharmaceutical agents. It is often employed in the synthesis of compounds targeting neurological disorders, as the piperidine scaffold is a common feature in drugs affecting the central nervous system. Additionally, the difluoro group can enhance the metabolic stability and bioavailability of the resulting molecules. Researchers also explore its use in agrochemical research for creating novel pesticides or herbicides, leveraging its unique chemical properties to improve efficacy and selectivity.
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