N-(1R,2S)-1-[4-(6-Cyano-3-pyridinyl)phenyl]-3-fluoro-1-hydroxy-2-propanyl-2,2-difluoroacetamide
95%
- Product Code: 55034
CAS:
605650-19-9
| Molecular Weight: | 349.31 g./mol | Molecular Formula: | C₁₇H₁₄F₃N₃O₂ |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 621.1±55.0 °C(Predicted) | |
| Density: | 1.38±0.1 g/cm3(Predicted) | Storage Condition: | 2-8℃ |
Product Description:
This compound is primarily utilized in the development of pharmaceuticals, particularly in the research and synthesis of novel therapeutic agents. Its unique structure, featuring a cyano-pyridinyl group and difluoroacetamide moiety, makes it a valuable intermediate in the creation of targeted drugs. It is often explored for its potential in treating neurological disorders, as the pyridine ring and fluorine atoms enhance its ability to cross the blood-brain barrier. Additionally, its fluorinated components are of interest in the design of anti-inflammatory and anti-cancer medications, where fluorine atoms can improve metabolic stability and binding affinity to biological targets. Researchers also investigate its use in enzyme inhibition studies, leveraging its specific molecular interactions to modulate biochemical pathways.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.001 | 10-20 days | $858.86 |
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N-(1R,2S)-1-[4-(6-Cyano-3-pyridinyl)phenyl]-3-fluoro-1-hydroxy-2-propanyl-2,2-difluoroacetamide
This compound is primarily utilized in the development of pharmaceuticals, particularly in the research and synthesis of novel therapeutic agents. Its unique structure, featuring a cyano-pyridinyl group and difluoroacetamide moiety, makes it a valuable intermediate in the creation of targeted drugs. It is often explored for its potential in treating neurological disorders, as the pyridine ring and fluorine atoms enhance its ability to cross the blood-brain barrier. Additionally, its fluorinated components are of interest in the design of anti-inflammatory and anti-cancer medications, where fluorine atoms can improve metabolic stability and binding affinity to biological targets. Researchers also investigate its use in enzyme inhibition studies, leveraging its specific molecular interactions to modulate biochemical pathways.
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