N-[3,5-Bis(trifluoromethyl)phenyl]-N'-[(9R)-10,11-dihydro-6'-methoxycinchonan-9-yl]thiourea
98%
- Product Code: 70746
CAS:
871334-35-9
| Molecular Weight: | 596.63 g./mol | Molecular Formula: | C₂₉H₃₀F₆N₄OS |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD23704931 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, dark, inert gas |
Product Description:
This chemical is primarily utilized in asymmetric synthesis and catalysis, particularly in enantioselective reactions. It serves as a chiral thiourea catalyst, enabling the formation of stereochemically complex molecules with high selectivity. Its application is significant in pharmaceutical research, where it aids in the synthesis of chiral intermediates for drug development. Additionally, it is employed in organic chemistry to facilitate the construction of carbon-carbon and carbon-heteroatom bonds under mild conditions. Its trifluoromethyl groups enhance its catalytic efficiency and stability, making it a valuable tool in modern synthetic methodologies.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | ฿10,350.00 |
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N-[3,5-Bis(trifluoromethyl)phenyl]-N'-[(9R)-10,11-dihydro-6'-methoxycinchonan-9-yl]thiourea
This chemical is primarily utilized in asymmetric synthesis and catalysis, particularly in enantioselective reactions. It serves as a chiral thiourea catalyst, enabling the formation of stereochemically complex molecules with high selectivity. Its application is significant in pharmaceutical research, where it aids in the synthesis of chiral intermediates for drug development. Additionally, it is employed in organic chemistry to facilitate the construction of carbon-carbon and carbon-heteroatom bonds under mild conditions. Its trifluoromethyl groups enhance its catalytic efficiency and stability, making it a valuable tool in modern synthetic methodologies.
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