tert-Butyl 3-fluoro-5-(hydroxymethyl)piperidine-1-carboxylate
97%
- Product Code: 85320
CAS:
1241725-59-6
| Molecular Weight: | 233.28 g./mol | Molecular Formula: | C₁₁H₂₀FNO₃ |
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| EC Number: | MDL Number: | MFCD17015063 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This chemical is primarily utilized in the pharmaceutical and organic synthesis industries as a key intermediate in the development of various active pharmaceutical ingredients (APIs). Its structure, featuring a piperidine ring with functional groups like hydroxymethyl and fluoro, makes it valuable for designing and synthesizing compounds with potential therapeutic properties. It is often employed in the preparation of molecules targeting neurological disorders, such as anxiety, depression, or neurodegenerative diseases, due to its ability to interact with specific receptors in the central nervous system. Additionally, its tert-butyl carboxylate group provides stability and ease of manipulation during synthetic processes, making it a versatile building block in medicinal chemistry research.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $343.32 |
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| 0.250 | 10-20 days | $690.17 |
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tert-Butyl 3-fluoro-5-(hydroxymethyl)piperidine-1-carboxylate
This chemical is primarily utilized in the pharmaceutical and organic synthesis industries as a key intermediate in the development of various active pharmaceutical ingredients (APIs). Its structure, featuring a piperidine ring with functional groups like hydroxymethyl and fluoro, makes it valuable for designing and synthesizing compounds with potential therapeutic properties. It is often employed in the preparation of molecules targeting neurological disorders, such as anxiety, depression, or neurodegenerative diseases, due to its ability to interact with specific receptors in the central nervous system. Additionally, its tert-butyl carboxylate group provides stability and ease of manipulation during synthetic processes, making it a versatile building block in medicinal chemistry research.
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