(3R,4S)-tert-Butyl 3-fluoro-4-hydroxypiperidine-1-carboxylate
97%
- Product Code: 70897
CAS:
1174020-42-8
| Molecular Weight: | 219.25 g./mol | Molecular Formula: | C₁₀H₁₈FNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD18633012 | |
| 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 a fluorine atom and a hydroxyl group on the piperidine ring, makes it valuable for designing drugs with enhanced metabolic stability and binding affinity. It is often employed in the development of central nervous system (CNS) drugs, including potential treatments for neurological disorders such as Alzheimer’s disease and schizophrenia. Additionally, its tert-butyl carboxylate group provides a protective moiety that can be selectively removed during synthetic processes, enabling precise chemical modifications. Researchers also explore its use in creating novel compounds for targeting enzymes or receptors involved in disease pathways.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿5,400.00 |
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| 0.250 | 10-20 days | ฿9,000.00 |
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| 1.000 | 10-20 days | ฿22,770.00 |
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(3R,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 a fluorine atom and a hydroxyl group on the piperidine ring, makes it valuable for designing drugs with enhanced metabolic stability and binding affinity. It is often employed in the development of central nervous system (CNS) drugs, including potential treatments for neurological disorders such as Alzheimer’s disease and schizophrenia. Additionally, its tert-butyl carboxylate group provides a protective moiety that can be selectively removed during synthetic processes, enabling precise chemical modifications. Researchers also explore its use in creating novel compounds for targeting enzymes or receptors involved in disease pathways.
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