cis-tert-Butyl 3-fluoro-4-hydroxypyrrolidine-1-carboxylate
97%
- Product Code: 123401
CAS:
2055223-76-0
| Molecular Weight: | 205.23 g./mol | Molecular Formula: | C₉H₁₆FNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD18791199 | |
| Melting Point: | Boiling Point: | 282.3±40.0°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This compound is primarily utilized in the pharmaceutical and chemical research industries as a key intermediate in the synthesis of more complex molecules. Its structure, featuring a fluorinated pyrrolidine ring, makes it valuable for developing biologically active compounds, particularly in drug discovery. The presence of fluorine enhances the stability and bioavailability of potential drug candidates, while the hydroxyl group allows for further functionalization. It is often employed in the creation of enzyme inhibitors, receptor modulators, and other therapeutic agents targeting neurological and metabolic disorders. Additionally, its tert-butyl ester group provides protection during synthetic processes, ensuring selective reactivity in multi-step reactions.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | White To Off-White Solid |
| Purity (%) | 96.5-100 |
| Infrared Spectrum | Conforms To Structure |
| NMR | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿4,010.00 |
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| 0.250 | 10-20 days | ฿5,610.00 |
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| 1.000 | 10-20 days | ฿13,680.00 |
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cis-tert-Butyl 3-fluoro-4-hydroxypyrrolidine-1-carboxylate
This compound is primarily utilized in the pharmaceutical and chemical research industries as a key intermediate in the synthesis of more complex molecules. Its structure, featuring a fluorinated pyrrolidine ring, makes it valuable for developing biologically active compounds, particularly in drug discovery. The presence of fluorine enhances the stability and bioavailability of potential drug candidates, while the hydroxyl group allows for further functionalization. It is often employed in the creation of enzyme inhibitors, receptor modulators, and other therapeutic agents targeting neurological and metabolic disorders. Additionally, its tert-butyl ester group provides protection during synthetic processes, ensuring selective reactivity in multi-step reactions.
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