1,1,1-Trifluoro-N-[(11bS)-4-oxido-2,6-bis[2,4,6-trisisopropylphenyl]dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-yl]methanesulfonamide
≥98%,≥99% e.e.
- Product Code: 70562
CAS:
908338-43-2
| Molecular Weight: | 884 g./mol | Molecular Formula: | C₅₁H₅₇F₃NO₅PS |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 835.3±75.0 °C | |
| Density: | 1.26±0.1 g/mL | Storage Condition: | room temperature, dry |
Product Description:
This compound is primarily utilized in advanced organic synthesis, particularly as a chiral ligand or catalyst in asymmetric transformations. Its unique structure, featuring bulky isopropyl groups and a trifluoromethylsulfonamide moiety, makes it highly effective in controlling stereochemistry during reactions. It is often employed in the synthesis of complex molecules, such as pharmaceuticals or fine chemicals, where precise enantioselectivity is critical. Additionally, its stability and resistance to harsh reaction conditions make it suitable for use in demanding catalytic processes, including hydrogenation, cross-coupling, and C-H activation reactions.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.025 | 10-20 days | ฿8,900.00 |
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| 0.100 | 10-20 days | ฿24,000.00 |
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1,1,1-Trifluoro-N-[(11bS)-4-oxido-2,6-bis[2,4,6-trisisopropylphenyl]dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-yl]methanesulfonamide
This compound is primarily utilized in advanced organic synthesis, particularly as a chiral ligand or catalyst in asymmetric transformations. Its unique structure, featuring bulky isopropyl groups and a trifluoromethylsulfonamide moiety, makes it highly effective in controlling stereochemistry during reactions. It is often employed in the synthesis of complex molecules, such as pharmaceuticals or fine chemicals, where precise enantioselectivity is critical. Additionally, its stability and resistance to harsh reaction conditions make it suitable for use in demanding catalytic processes, including hydrogenation, cross-coupling, and C-H activation reactions.
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