(S)-4-((S)-sec-Butyl)-2-(pyridin-2-yl)-4,5-dihydrooxazole
98%
- Product Code: 123728
CAS:
108915-03-3
| Molecular Weight: | 204.27 g./mol | Molecular Formula: | C₁₂H₁₆N₂O |
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| Density: | Storage Condition: | 2-8°C, protected from light, inert gas |
Product Description:
This compound is primarily utilized in the field of asymmetric synthesis and catalysis, where it serves as a chiral ligand. Its structure, featuring a dihydrooxazole ring and a pyridine moiety, makes it effective in coordinating with metal centers, particularly in transition metal-catalyzed reactions. It is often employed in enantioselective transformations, such as hydrogenation, carbon-carbon bond formation, and other stereospecific processes, enhancing the production of chiral molecules with high optical purity. Its application is significant in pharmaceutical synthesis, where precise control over stereochemistry is crucial for the development of active pharmaceutical ingredients (APIs). Additionally, it is explored in materials science for designing chiral catalysts and frameworks.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿4,797.00 |
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(S)-4-((S)-sec-Butyl)-2-(pyridin-2-yl)-4,5-dihydrooxazole
This compound is primarily utilized in the field of asymmetric synthesis and catalysis, where it serves as a chiral ligand. Its structure, featuring a dihydrooxazole ring and a pyridine moiety, makes it effective in coordinating with metal centers, particularly in transition metal-catalyzed reactions. It is often employed in enantioselective transformations, such as hydrogenation, carbon-carbon bond formation, and other stereospecific processes, enhancing the production of chiral molecules with high optical purity. Its application is significant in pharmaceutical synthesis, where precise control over stereochemistry is crucial for the development of active pharmaceutical ingredients (APIs). Additionally, it is explored in materials science for designing chiral catalysts and frameworks.
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