(11bR)-N-(2,6-Bis(4-nitrophenyl)-4-oxidodinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-yl)-1,1,1-trifluoromethanesulfonamide
97%
- Product Code: 123589
CAS:
1010799-99-1
| Molecular Weight: | 721.55 g./mol | Molecular Formula: | C₃₃H₁₉F₃N₃O₉PS |
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| Density: | Storage Condition: | Room temperature, sealed, dry, dark |
Product Description:
This compound is primarily utilized in advanced organic synthesis and catalysis, particularly in the development of asymmetric reactions. Its unique structure, featuring a dioxaphosphepin core and trifluoromethanesulfonamide group, makes it an effective chiral ligand or catalyst in enantioselective transformations. It is often employed in the synthesis of complex molecules, such as pharmaceuticals and fine chemicals, where high stereochemical control is required. Additionally, its electron-withdrawing nitro groups enhance its reactivity in coupling reactions and other catalytic processes. The compound's stability and selectivity make it valuable in research and industrial applications focused on producing optically active compounds.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.050 | 10-20 days | ฿4,707.00 |
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| 0.100 | 10-20 days | ฿7,056.00 |
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| 0.250 | 10-20 days | ฿11,286.00 |
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(11bR)-N-(2,6-Bis(4-nitrophenyl)-4-oxidodinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-yl)-1,1,1-trifluoromethanesulfonamide
This compound is primarily utilized in advanced organic synthesis and catalysis, particularly in the development of asymmetric reactions. Its unique structure, featuring a dioxaphosphepin core and trifluoromethanesulfonamide group, makes it an effective chiral ligand or catalyst in enantioselective transformations. It is often employed in the synthesis of complex molecules, such as pharmaceuticals and fine chemicals, where high stereochemical control is required. Additionally, its electron-withdrawing nitro groups enhance its reactivity in coupling reactions and other catalytic processes. The compound's stability and selectivity make it valuable in research and industrial applications focused on producing optically active compounds.
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