(3S,4S)-tert-Butyl 3-amino-4-fluoropiperidine-1-carboxylate
97%
- Product Code: 36784
CAS:
1290191-71-7
| Molecular Weight: | 218.27 g./mol | Molecular Formula: | C₁₀H₁₉FN₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28010923 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, protected from light, stored in an inert gas |
Product Description:
This chemical is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various biologically active compounds. Its structure, featuring both amino and fluoro substituents on the piperidine ring, makes it valuable for developing drug candidates, particularly those targeting central nervous system disorders, cardiovascular diseases, and infectious diseases. The tert-butyl carbamate group serves as a protective group for the amine, allowing for selective reactions during complex molecule synthesis. Its stereochemistry (3S,4S) is crucial for achieving the desired pharmacological activity in chiral drug molecules. Additionally, its fluorine atom enhances the metabolic stability and bioavailability of the final drug products. This compound is often employed in medicinal chemistry research to optimize drug potency, selectivity, and pharmacokinetic properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿4,932.00 |
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| 0.250 | 10-20 days | ฿7,902.00 |
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| 1.000 | 10-20 days | ฿19,791.00 |
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(3S,4S)-tert-Butyl 3-amino-4-fluoropiperidine-1-carboxylate
This chemical is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various biologically active compounds. Its structure, featuring both amino and fluoro substituents on the piperidine ring, makes it valuable for developing drug candidates, particularly those targeting central nervous system disorders, cardiovascular diseases, and infectious diseases. The tert-butyl carbamate group serves as a protective group for the amine, allowing for selective reactions during complex molecule synthesis. Its stereochemistry (3S,4S) is crucial for achieving the desired pharmacological activity in chiral drug molecules. Additionally, its fluorine atom enhances the metabolic stability and bioavailability of the final drug products. This compound is often employed in medicinal chemistry research to optimize drug potency, selectivity, and pharmacokinetic properties.
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