(3S,4S)-tert-Butyl 3-fluoro-4-hydroxypiperidine-1-carboxylate
97%
- Product Code: 70919
CAS:
1174020-44-0
| Molecular Weight: | 219.25 g./mol | Molecular Formula: | C₁₀H₁₈FNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD18632749 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various biologically active molecules. Its unique structure, featuring both fluorine and hydroxyl groups on a piperidine ring, makes it valuable for developing drugs with enhanced metabolic stability and binding affinity. It is often employed in the production of enzyme inhibitors, receptor antagonists, and other therapeutic agents targeting neurological and cardiovascular diseases. Additionally, its tert-butyl carbamate group provides a protective function during multi-step synthetic processes, ensuring the integrity of the molecule until the final deprotection stage. Its applications are particularly significant in the development of compounds with improved pharmacokinetic properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿3,789.00 |
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| 0.250 | 10-20 days | ฿6,435.00 |
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| 1.000 | 10-20 days | ฿17,361.00 |
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(3S,4S)-tert-Butyl 3-fluoro-4-hydroxypiperidine-1-carboxylate
This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various biologically active molecules. Its unique structure, featuring both fluorine and hydroxyl groups on a piperidine ring, makes it valuable for developing drugs with enhanced metabolic stability and binding affinity. It is often employed in the production of enzyme inhibitors, receptor antagonists, and other therapeutic agents targeting neurological and cardiovascular diseases. Additionally, its tert-butyl carbamate group provides a protective function during multi-step synthetic processes, ensuring the integrity of the molecule until the final deprotection stage. Its applications are particularly significant in the development of compounds with improved pharmacokinetic properties.
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