(11bR)-N-(2, 6-di([1, 1'-biphenyl]-4-yl)-4-oXndo-8, 9, 10, 11, 12, 13, 14, 15-octahydrodinaphtho[2, 1-d: 1', 2'-f][1, 3, 2]dioxaphosphepin-4-yl)-1, 1, 1-trifluoromethanesulfonamide
97%
- Product Code: 231105
CAS:
1261302-63-9
| Molecular Weight: | 793.82 g./mol | Molecular Formula: | C₄₅H₃₉F₃NO₅PS |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD33021036 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, dry, light-proof |
Product Description:
Used as a chiral catalyst ligand in asymmetric synthesis, particularly in enantioselective transition metal-catalyzed reactions. Its rigid, sterically hindered structure enables high enantioselectivity in transformations such as hydrogenations, C–C bond formations, and cross-coupling reactions. Commonly employed in pharmaceutical synthesis where precise stereochemical control is critical. The trifluoromethanesulfonamide group enhances stability and coordination ability with metals like palladium, rhodium, or iridium, making it suitable for demanding catalytic conditions. Also utilized in the development of novel catalytic systems for fine chemical production.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿4,500.00 |
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| 0.250 | 10-20 days | ฿11,080.00 |
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(11bR)-N-(2, 6-di([1, 1'-biphenyl]-4-yl)-4-oXndo-8, 9, 10, 11, 12, 13, 14, 15-octahydrodinaphtho[2, 1-d: 1', 2'-f][1, 3, 2]dioxaphosphepin-4-yl)-1, 1, 1-trifluoromethanesulfonamide
Used as a chiral catalyst ligand in asymmetric synthesis, particularly in enantioselective transition metal-catalyzed reactions. Its rigid, sterically hindered structure enables high enantioselectivity in transformations such as hydrogenations, C–C bond formations, and cross-coupling reactions. Commonly employed in pharmaceutical synthesis where precise stereochemical control is critical. The trifluoromethanesulfonamide group enhances stability and coordination ability with metals like palladium, rhodium, or iridium, making it suitable for demanding catalytic conditions. Also utilized in the development of novel catalytic systems for fine chemical production.
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