(S)-2,2'-Bis[bis(3,5-trifluoromethylphenyl)phosphino]-4,4',6,6'-tetramethoxy)-1,1'-biphenyl
98%
- Product Code: 37995
CAS:
1365531-85-6
| Molecular Weight: | 1186.6427 g./mol | Molecular Formula: | C₄₈H₂₈F₂₄O₄P₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD19443625 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It is highly effective in facilitating enantioselective transformations, such as hydrogenation, carbon-carbon bond formation, and other organic synthesis processes. Its electron-rich and sterically demanding structure allows for precise control over the stereochemistry of the reaction products, making it valuable in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. The trifluoromethyl groups enhance its stability and reactivity, while the methoxy groups contribute to its solubility and ligand-metal coordination properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿6,732.00 |
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(S)-2,2'-Bis[bis(3,5-trifluoromethylphenyl)phosphino]-4,4',6,6'-tetramethoxy)-1,1'-biphenyl
This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It is highly effective in facilitating enantioselective transformations, such as hydrogenation, carbon-carbon bond formation, and other organic synthesis processes. Its electron-rich and sterically demanding structure allows for precise control over the stereochemistry of the reaction products, making it valuable in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. The trifluoromethyl groups enhance its stability and reactivity, while the methoxy groups contribute to its solubility and ligand-metal coordination properties.
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