(3S,4R)-rel-tert-Butyl 3-fluoro-4-(hydroxymethyl)piperidine-1-carboxylate
98%
- Product Code: 126385
CAS:
882033-93-4
| Molecular Weight: | 233.28 g./mol | Molecular Formula: | C11H20FNO3 |
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| EC Number: | MDL Number: | MFCD24850020 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This compound is primarily utilized in pharmaceutical research and development as a key intermediate in the synthesis of biologically active molecules. Its unique structure, featuring a fluorine atom and a hydroxymethyl group on a piperidine ring, makes it valuable for designing drugs targeting central nervous system disorders, such as neurodegenerative diseases or psychiatric conditions. The tert-butyl carboxylate group enhances its stability during chemical reactions, making it suitable for multi-step synthetic processes. Researchers also explore its potential in creating enzyme inhibitors or receptor modulators due to its ability to interact with specific biological targets. Its applications extend to the development of novel therapeutic agents with improved efficacy and selectivity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.250 | 10-20 days | £273.21 |
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| 1.000 | 10-20 days | £736.86 |
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(3S,4R)-rel-tert-Butyl 3-fluoro-4-(hydroxymethyl)piperidine-1-carboxylate
This compound is primarily utilized in pharmaceutical research and development as a key intermediate in the synthesis of biologically active molecules. Its unique structure, featuring a fluorine atom and a hydroxymethyl group on a piperidine ring, makes it valuable for designing drugs targeting central nervous system disorders, such as neurodegenerative diseases or psychiatric conditions. The tert-butyl carboxylate group enhances its stability during chemical reactions, making it suitable for multi-step synthetic processes. Researchers also explore its potential in creating enzyme inhibitors or receptor modulators due to its ability to interact with specific biological targets. Its applications extend to the development of novel therapeutic agents with improved efficacy and selectivity.
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