(S)-4-Isopropyl-2-(1,10-phenanthrolin-2-yl)-4,5-dihydrooxazole
98%
- Product Code: 38511
CAS:
1562372-40-0
| Molecular Weight: | 291.3471 g./mol | Molecular Formula: | C₁₈H₁₇N₃O |
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| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in asymmetric catalysis, particularly in enantioselective synthesis, where it serves as a chiral ligand. Its structure, featuring a phenanthroline moiety and an oxazoline ring, makes it effective in coordinating with metal ions, such as copper or palladium, to form stable complexes. These complexes are employed in various organic transformations, including cyclopropanation, allylic alkylation, and Diels-Alder reactions, where high enantioselectivity is required. Additionally, it finds application in the development of chiral catalysts for pharmaceutical synthesis, enabling the production of enantiomerically pure compounds. Its stability and efficiency in catalytic systems make it a valuable tool in the field of organic and medicinal chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿9,702.00 |
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(S)-4-Isopropyl-2-(1,10-phenanthrolin-2-yl)-4,5-dihydrooxazole
This compound is primarily utilized in asymmetric catalysis, particularly in enantioselective synthesis, where it serves as a chiral ligand. Its structure, featuring a phenanthroline moiety and an oxazoline ring, makes it effective in coordinating with metal ions, such as copper or palladium, to form stable complexes. These complexes are employed in various organic transformations, including cyclopropanation, allylic alkylation, and Diels-Alder reactions, where high enantioselectivity is required. Additionally, it finds application in the development of chiral catalysts for pharmaceutical synthesis, enabling the production of enantiomerically pure compounds. Its stability and efficiency in catalytic systems make it a valuable tool in the field of organic and medicinal chemistry.
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