N,N'-[(1R,2R)-1,2-Diphenyl-1,2-ethanediyl]bis[N'-[3,5-bis(trifluoromethyl)phenyl]thiourea]
≥98%,99%e.e.
- Product Code: 70663
CAS:
1012051-90-9
| Molecular Weight: | 754.7 g./mol | Molecular Formula: | C₃₂H₂₂F₁₂N₄S₂ |
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| Melting Point: | 194-196°C | Boiling Point: | |
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This chemical is primarily utilized as a chiral catalyst or chiral auxiliary in asymmetric synthesis. Its unique structure, featuring thiourea groups and trifluoromethylphenyl moieties, makes it highly effective in promoting enantioselective reactions. It is commonly employed in organic synthesis to control the stereochemistry of products, particularly in the formation of chiral centers. The compound is often used in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals where high enantiomeric purity is critical. Its ability to form hydrogen bonds and interact with substrates selectively enhances its efficiency in catalytic processes, making it a valuable tool in modern synthetic chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | £193.60 |
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N,N'-[(1R,2R)-1,2-Diphenyl-1,2-ethanediyl]bis[N'-[3,5-bis(trifluoromethyl)phenyl]thiourea]
This chemical is primarily utilized as a chiral catalyst or chiral auxiliary in asymmetric synthesis. Its unique structure, featuring thiourea groups and trifluoromethylphenyl moieties, makes it highly effective in promoting enantioselective reactions. It is commonly employed in organic synthesis to control the stereochemistry of products, particularly in the formation of chiral centers. The compound is often used in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals where high enantiomeric purity is critical. Its ability to form hydrogen bonds and interact with substrates selectively enhances its efficiency in catalytic processes, making it a valuable tool in modern synthetic chemistry.
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