N-[(1R,2R)-2-aMino-1,2-diphenylethyl]-N'-[3,5-bis(trifluoroMethyl)phenyl]-Thiourea
98%
- Product Code: 70691
CAS:
1088705-53-6
| Molecular Weight: | 483.5 g./mol | Molecular Formula: | C₂₃H₁₉F₆N₃S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD30541721 | |
| Melting Point: | 91-93 °C | Boiling Point: | 487.6±55.0 °C |
| Density: | 1.384±0.06 g/cm3 | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in asymmetric synthesis and catalysis, particularly in enantioselective reactions. It serves as a chiral thiourea catalyst, enabling the formation of enantiomerically pure compounds, which are crucial in the production of pharmaceuticals and fine chemicals. Its ability to form hydrogen bonds with substrates makes it effective in activating electrophiles and stabilizing intermediates, enhancing reaction efficiency and selectivity. Additionally, it is employed in the development of novel catalytic systems for organic transformations, contributing to advancements in green chemistry and sustainable processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | $161.46 |
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N-[(1R,2R)-2-aMino-1,2-diphenylethyl]-N'-[3,5-bis(trifluoroMethyl)phenyl]-Thiourea
This compound is primarily utilized in asymmetric synthesis and catalysis, particularly in enantioselective reactions. It serves as a chiral thiourea catalyst, enabling the formation of enantiomerically pure compounds, which are crucial in the production of pharmaceuticals and fine chemicals. Its ability to form hydrogen bonds with substrates makes it effective in activating electrophiles and stabilizing intermediates, enhancing reaction efficiency and selectivity. Additionally, it is employed in the development of novel catalytic systems for organic transformations, contributing to advancements in green chemistry and sustainable processes.
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