N-[3,5-Bis(trifluoromethyl)phenyl]-N'-(8α,9S)-cinchonan-9-ylthiourea
≥98%,99%d.e.
- Product Code: 70742
CAS:
890044-38-9
| Molecular Weight: | 564.6 g./mol | Molecular Formula: | C₂₈H₂₆F₆N₄S |
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| Density: | Storage Condition: | room temperature, dry |
Product Description:
This compound is primarily utilized in asymmetric catalysis, particularly in enantioselective reactions. It serves as a chiral thiourea catalyst, enabling the synthesis of complex molecules with high stereochemical control. Its application is prominent in the pharmaceutical industry for the production of enantiomerically pure drugs, where precise stereochemistry is crucial for efficacy and safety. Additionally, it is employed in organic synthesis for constructing chiral intermediates used in natural product synthesis and fine chemicals. Its unique structure allows it to act as a hydrogen-bond donor, facilitating the activation of substrates and enhancing reaction selectivity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿13,230.00 |
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N-[3,5-Bis(trifluoromethyl)phenyl]-N'-(8α,9S)-cinchonan-9-ylthiourea
This compound is primarily utilized in asymmetric catalysis, particularly in enantioselective reactions. It serves as a chiral thiourea catalyst, enabling the synthesis of complex molecules with high stereochemical control. Its application is prominent in the pharmaceutical industry for the production of enantiomerically pure drugs, where precise stereochemistry is crucial for efficacy and safety. Additionally, it is employed in organic synthesis for constructing chiral intermediates used in natural product synthesis and fine chemicals. Its unique structure allows it to act as a hydrogen-bond donor, facilitating the activation of substrates and enhancing reaction selectivity.
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