1,1,1-Trifluoro-N-[(11bR)-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: 70561
CAS:
1239466-15-9
| 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 chemical is primarily utilized in advanced organic synthesis, particularly in asymmetric catalysis. Its unique structure, featuring bulky substituents and a trifluoromethyl group, makes it highly effective in facilitating enantioselective reactions. It is often employed in the synthesis of chiral molecules, which are crucial in the production of pharmaceuticals, agrochemicals, and fine chemicals. The compound's ability to stabilize transition states and enhance selectivity makes it a valuable tool in the development of complex organic compounds with high stereochemical purity. Additionally, its application extends to materials science, where it is used in the design of specialized ligands for metal-catalyzed processes, contributing to the creation of novel polymeric and coordination compounds.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Off-white to light yellow Solid |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | £538.96 |
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| 0.500 | 10-20 days | £1,582.96 |
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1,1,1-Trifluoro-N-[(11bR)-4-oxido-2,6-bis[2,4,6-trisisopropylphenyl]dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-yl]methanesulfonamide
This chemical is primarily utilized in advanced organic synthesis, particularly in asymmetric catalysis. Its unique structure, featuring bulky substituents and a trifluoromethyl group, makes it highly effective in facilitating enantioselective reactions. It is often employed in the synthesis of chiral molecules, which are crucial in the production of pharmaceuticals, agrochemicals, and fine chemicals. The compound's ability to stabilize transition states and enhance selectivity makes it a valuable tool in the development of complex organic compounds with high stereochemical purity. Additionally, its application extends to materials science, where it is used in the design of specialized ligands for metal-catalyzed processes, contributing to the creation of novel polymeric and coordination compounds.
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