N-[(11bR)-2,6-Bis[3,5-bis(trifluoromethyl)phenyl]-8,9,10,11,12,13,14,15-octahydro-4-oxido-dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-yl]-1,1,1-trifluoromethanesulfonamide
≥98%,≥99% e.e.
- Product Code: 57514
CAS:
1261302-64-0
| Molecular Weight: | 911.6 g./mol | Molecular Formula: | C₃₇H₂₅F₁₅NO₅PS |
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| EC Number: | MDL Number: | ||
| Melting Point: | 188-192 °C | Boiling Point: | |
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This compound is primarily utilized in asymmetric catalysis, particularly in enantioselective synthesis. Its complex structure and chiral environment make it highly effective in facilitating reactions where the formation of a specific enantiomer is crucial. It is often employed in the synthesis of pharmaceuticals and fine chemicals, where precise control over stereochemistry is essential. Additionally, its trifluoromethyl groups enhance its stability and reactivity, making it suitable for use under harsh reaction conditions. The compound’s unique phosphine oxide moiety further contributes to its role as a ligand in transition metal catalysis, enabling efficient and selective transformations in organic synthesis.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | €276.75 |
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| 0.250 | 10-20 days | €525.27 |
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N-[(11bR)-2,6-Bis[3,5-bis(trifluoromethyl)phenyl]-8,9,10,11,12,13,14,15-octahydro-4-oxido-dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-yl]-1,1,1-trifluoromethanesulfonamide
This compound is primarily utilized in asymmetric catalysis, particularly in enantioselective synthesis. Its complex structure and chiral environment make it highly effective in facilitating reactions where the formation of a specific enantiomer is crucial. It is often employed in the synthesis of pharmaceuticals and fine chemicals, where precise control over stereochemistry is essential. Additionally, its trifluoromethyl groups enhance its stability and reactivity, making it suitable for use under harsh reaction conditions. The compound’s unique phosphine oxide moiety further contributes to its role as a ligand in transition metal catalysis, enabling efficient and selective transformations in organic synthesis.
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