N-[3,5-Bis(trifluoromethyl)phenyl]-N'-(9R)-cinchonan-9-ylthiourea
≥98%,99%d.e.
- Product Code: 70745
CAS:
851477-19-5
| Molecular Weight: | 564.6 g./mol | Molecular Formula: | C₂₈H₂₆F₆N₄S |
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| Density: | Storage Condition: | room temperature, dry |
Product Description:
This chemical is primarily utilized as a chiral catalyst or chiral auxiliary in asymmetric synthesis, particularly in enantioselective reactions. Its unique structure, featuring a cinchona alkaloid backbone and trifluoromethylphenyl groups, makes it highly effective in inducing chirality in various organic transformations. It is often employed in the synthesis of pharmaceuticals and fine chemicals where precise control over stereochemistry is crucial. Additionally, it finds application in the development of chiral ligands for metal-catalyzed reactions, enhancing selectivity and yield in complex synthetic pathways. Its use extends to research and development in organic chemistry, particularly in the exploration of novel catalytic processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿25,110.00 |
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N-[3,5-Bis(trifluoromethyl)phenyl]-N'-(9R)-cinchonan-9-ylthiourea
This chemical is primarily utilized as a chiral catalyst or chiral auxiliary in asymmetric synthesis, particularly in enantioselective reactions. Its unique structure, featuring a cinchona alkaloid backbone and trifluoromethylphenyl groups, makes it highly effective in inducing chirality in various organic transformations. It is often employed in the synthesis of pharmaceuticals and fine chemicals where precise control over stereochemistry is crucial. Additionally, it finds application in the development of chiral ligands for metal-catalyzed reactions, enhancing selectivity and yield in complex synthetic pathways. Its use extends to research and development in organic chemistry, particularly in the exploration of novel catalytic processes.
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