N,N'-[(1S,2S)-1,2-Diphenyl-1,2-ethanediyl]bis[N'-[3,5-bis(trifluoromethyl)phenyl]thiourea]
≥95%,99%e.e.
- Product Code: 70666
CAS:
1416334-72-9
| Molecular Weight: | 754.7 g./mol | Molecular Formula: | C₃₂H₂₂F₁₂N₄S₂ |
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| Density: | Storage Condition: | room temperature, dry |
Product Description:
This compound is primarily utilized in asymmetric catalysis and chiral recognition processes. Its unique structural features make it highly effective in enantioselective reactions, particularly in the synthesis of chiral molecules. It is often employed as a chiral catalyst or ligand in organic transformations, such as hydrogenation, alkylation, and cyclization reactions, where high enantiomeric purity is required. Additionally, its thiourea moiety enables strong hydrogen bonding interactions, making it useful in molecular recognition and sensing applications for specific substrates. Its trifluoromethyl groups enhance its solubility in organic solvents, facilitating its use in various synthetic protocols.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿7,713.00 |
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N,N'-[(1S,2S)-1,2-Diphenyl-1,2-ethanediyl]bis[N'-[3,5-bis(trifluoromethyl)phenyl]thiourea]
This compound is primarily utilized in asymmetric catalysis and chiral recognition processes. Its unique structural features make it highly effective in enantioselective reactions, particularly in the synthesis of chiral molecules. It is often employed as a chiral catalyst or ligand in organic transformations, such as hydrogenation, alkylation, and cyclization reactions, where high enantiomeric purity is required. Additionally, its thiourea moiety enables strong hydrogen bonding interactions, making it useful in molecular recognition and sensing applications for specific substrates. Its trifluoromethyl groups enhance its solubility in organic solvents, facilitating its use in various synthetic protocols.
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