RuCl(p-cymene)[(S,S)-Ts-DPEN]
95%
- Product Code: 65702
CAS:
192139-90-5
| Molecular Weight: | 636.21 g./mol | Molecular Formula: | C₃₁H₃₅ClN₂O₂RuS |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09953484 | |
| Melting Point: | >175 °C | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily used as a catalyst in asymmetric hydrogenation reactions, which are crucial in the synthesis of chiral molecules. These reactions are widely applied in the pharmaceutical industry to produce enantiomerically pure compounds, which are essential for the development of drugs with specific biological activities. The chiral nature of the catalyst allows for high selectivity and efficiency in the production of complex organic molecules, making it valuable in the synthesis of active pharmaceutical ingredients (APIs). Additionally, it is utilized in academic research to explore new methodologies in asymmetric catalysis, contributing to advancements in synthetic organic chemistry.
Product Specification:
| Test | Specification |
|---|---|
| Purity | 95 100% |
| APPEARANCE | ORANGE TO VERY DARK BROWN POWDER OR SOLID |
| INFRARED SPECTRUM | Conforms to Structure |
| PROTON NMR SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿920.00 |
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| 0.500 | 10-20 days | ฿2,880.00 |
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| 2.000 | 10-20 days | ฿8,600.00 |
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RuCl(p-cymene)[(S,S)-Ts-DPEN]
This chemical is primarily used as a catalyst in asymmetric hydrogenation reactions, which are crucial in the synthesis of chiral molecules. These reactions are widely applied in the pharmaceutical industry to produce enantiomerically pure compounds, which are essential for the development of drugs with specific biological activities. The chiral nature of the catalyst allows for high selectivity and efficiency in the production of complex organic molecules, making it valuable in the synthesis of active pharmaceutical ingredients (APIs). Additionally, it is utilized in academic research to explore new methodologies in asymmetric catalysis, contributing to advancements in synthetic organic chemistry.
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