(S)-4-(tert-Butyl)-2-(4-(trifluoromethyl)pyridin-2-yl)-4,5-dihydrooxazole
98%
- Product Code: 57570
CAS:
1257527-14-2
| Molecular Weight: | 272.27 g./mol | Molecular Formula: | C₁₃H₁₅F₃N₂O |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | 56-59 °C | Boiling Point: | 335.7±42.0 °C |
| Density: | 1.25±0.1 g/cm3 | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in the field of organic synthesis, particularly as a chiral ligand or catalyst in asymmetric reactions. It plays a significant role in the production of enantiomerically pure compounds, which are crucial in the development of pharmaceuticals, agrochemicals, and fine chemicals. Its structure, featuring a dihydrooxazole ring and a trifluoromethylpyridine moiety, enhances its ability to induce stereoselectivity in various catalytic processes, such as hydrogenation, cyclopropanation, and carbon-carbon bond formation. Additionally, its tert-butyl group contributes to increased stability and steric hindrance, making it effective in controlling the spatial arrangement of reactants during synthesis. This chemical is also explored in material science for designing advanced chiral materials with potential applications in optoelectronics and sensors.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | ฿8,892.00 |
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(S)-4-(tert-Butyl)-2-(4-(trifluoromethyl)pyridin-2-yl)-4,5-dihydrooxazole
This compound is primarily utilized in the field of organic synthesis, particularly as a chiral ligand or catalyst in asymmetric reactions. It plays a significant role in the production of enantiomerically pure compounds, which are crucial in the development of pharmaceuticals, agrochemicals, and fine chemicals. Its structure, featuring a dihydrooxazole ring and a trifluoromethylpyridine moiety, enhances its ability to induce stereoselectivity in various catalytic processes, such as hydrogenation, cyclopropanation, and carbon-carbon bond formation. Additionally, its tert-butyl group contributes to increased stability and steric hindrance, making it effective in controlling the spatial arrangement of reactants during synthesis. This chemical is also explored in material science for designing advanced chiral materials with potential applications in optoelectronics and sensors.
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