(R)-2,2'-Bis[bis(3,5-trifluoromethylphenyl)phosphino]-4,4',6,6'-tetramethoxy)-1,1'-biphenyl
98%
- Product Code: 68652
CAS:
1365531-84-5
| Molecular Weight: | 1186.64 g./mol | Molecular Formula: | C₄₈H₂₈F₂₄O₄P₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD19443625 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
This compound is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure, featuring electron-withdrawing trifluoromethyl groups and methoxy substituents, enhances its effectiveness in facilitating enantioselective transformations. It is commonly employed in hydrogenation, carbon-carbon bond formation, and other key synthetic processes where high enantiomeric purity is required. The ligand’s steric and electronic properties make it highly selective, enabling the production of chiral intermediates and active pharmaceutical ingredients (APIs) with exceptional precision. Its application is critical in the pharmaceutical and fine chemical industries, where achieving specific stereochemistry is essential for the efficacy and safety of the final products.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | €157.18 |
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| 0.250 | 10-20 days | €371.83 |
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| 1.000 | 10-20 days | €1,203.57 |
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(R)-2,2'-Bis[bis(3,5-trifluoromethylphenyl)phosphino]-4,4',6,6'-tetramethoxy)-1,1'-biphenyl
This compound is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure, featuring electron-withdrawing trifluoromethyl groups and methoxy substituents, enhances its effectiveness in facilitating enantioselective transformations. It is commonly employed in hydrogenation, carbon-carbon bond formation, and other key synthetic processes where high enantiomeric purity is required. The ligand’s steric and electronic properties make it highly selective, enabling the production of chiral intermediates and active pharmaceutical ingredients (APIs) with exceptional precision. Its application is critical in the pharmaceutical and fine chemical industries, where achieving specific stereochemistry is essential for the efficacy and safety of the final products.
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