(4R,4'R,5S,5'S)-2,2'-(Pentane-3,3-diyl)bis(4,5-diphenyl-4,5-dihydrooxazole)
97%
- Product Code: 36975
CAS:
1246401-51-3
| Molecular Weight: | 514.6567 g./mol | Molecular Formula: | C₃₅H₃₄N₂O₂ |
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| Density: | Storage Condition: | room temperature |
Product Description:
This chiral chemical is primarily utilized as a ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It is often employed in transition metal-catalyzed processes, such as hydrogenation, to produce chiral molecules with high optical purity. Its rigid and well-defined structure makes it effective in controlling the stereochemistry of the reaction, leading to the formation of specific enantiomers. This is especially valuable in the pharmaceutical industry, where the production of enantiomerically pure compounds is essential for drug development. Additionally, it has been explored in the synthesis of complex natural products and fine chemicals, where precise stereocontrol is required. Its application extends to research in organic chemistry, where it serves as a tool for developing new asymmetric methodologies.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | €86.43 |
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(4R,4'R,5S,5'S)-2,2'-(Pentane-3,3-diyl)bis(4,5-diphenyl-4,5-dihydrooxazole)
This chiral chemical is primarily utilized as a ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It is often employed in transition metal-catalyzed processes, such as hydrogenation, to produce chiral molecules with high optical purity. Its rigid and well-defined structure makes it effective in controlling the stereochemistry of the reaction, leading to the formation of specific enantiomers. This is especially valuable in the pharmaceutical industry, where the production of enantiomerically pure compounds is essential for drug development. Additionally, it has been explored in the synthesis of complex natural products and fine chemicals, where precise stereocontrol is required. Its application extends to research in organic chemistry, where it serves as a tool for developing new asymmetric methodologies.
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