(S)-3,3'-Bis(2,3,4,5,6-pentafluorophenyl)-1,1'-binaphthyl-2,2'-diyl hydrogenphosphate
≥98%,99%e.e.
- Product Code: 83001
CAS:
1882075-20-8
| Molecular Weight: | 680.38 g./mol | Molecular Formula: | C₃₂H₁₁F₁₀O₄P |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry, sealed |
Product Description:
This compound is primarily used as a chiral ligand in asymmetric catalysis, particularly in enantioselective synthesis reactions. It plays a crucial role in facilitating the formation of chiral molecules with high enantiomeric purity, which is essential in the production of pharmaceuticals, agrochemicals, and fine chemicals. Its unique structure, featuring pentafluorophenyl groups, enhances its stability and reactivity in catalytic processes. Additionally, it is employed in the development of advanced materials and as a component in chiral stationary phases for chromatographic separation of enantiomers. Its application extends to research and development in organic chemistry, where it aids in the exploration of novel synthetic pathways and the optimization of catalytic systems.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Whiteto brown solid |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.020 | 10-20 days | ฿6,210.00 |
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| 0.100 | 10-20 days | ฿22,600.00 |
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| 0.500 | 10-20 days | ฿61,200.00 |
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(S)-3,3'-Bis(2,3,4,5,6-pentafluorophenyl)-1,1'-binaphthyl-2,2'-diyl hydrogenphosphate
This compound is primarily used as a chiral ligand in asymmetric catalysis, particularly in enantioselective synthesis reactions. It plays a crucial role in facilitating the formation of chiral molecules with high enantiomeric purity, which is essential in the production of pharmaceuticals, agrochemicals, and fine chemicals. Its unique structure, featuring pentafluorophenyl groups, enhances its stability and reactivity in catalytic processes. Additionally, it is employed in the development of advanced materials and as a component in chiral stationary phases for chromatographic separation of enantiomers. Its application extends to research and development in organic chemistry, where it aids in the exploration of novel synthetic pathways and the optimization of catalytic systems.
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