tert-Butyl 4-(2-ethoxy-2-oxoethyl)-3-fluoropiperidine-1-carboxylate
95%
- Product Code: 83777
CAS:
317360-04-6
| Molecular Weight: | 289.343 g./mol | Molecular Formula: | C₁₄H₂₄FNO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD18632740 | |
| Melting Point: | Boiling Point: | 346.3±27.0 °C at 760 mmHg | |
| Density: | 1.1±0.1 g/cm3 | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in the field of organic synthesis, particularly as an intermediate in the development of more complex chemical structures. Its unique structure, featuring both a fluoropiperidine ring and an ethoxy ester group, makes it valuable for constructing pharmacologically active molecules. It is often employed in the synthesis of potential drug candidates, especially those targeting neurological or cardiovascular systems. The fluorine atom enhances the compound's ability to interact with biological targets, while the ester group provides a reactive site for further chemical modifications. Researchers also use it in the study of enzyme inhibition and receptor binding due to its versatile reactivity and stability under various conditions.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | £305.33 |
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| 0.250 | 10-20 days | £549.59 |
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tert-Butyl 4-(2-ethoxy-2-oxoethyl)-3-fluoropiperidine-1-carboxylate
This compound is primarily utilized in the field of organic synthesis, particularly as an intermediate in the development of more complex chemical structures. Its unique structure, featuring both a fluoropiperidine ring and an ethoxy ester group, makes it valuable for constructing pharmacologically active molecules. It is often employed in the synthesis of potential drug candidates, especially those targeting neurological or cardiovascular systems. The fluorine atom enhances the compound's ability to interact with biological targets, while the ester group provides a reactive site for further chemical modifications. Researchers also use it in the study of enzyme inhibition and receptor binding due to its versatile reactivity and stability under various conditions.
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