(S)-3,3'-Bis(perfluorophenyl)-[1,1'-binaphthalene]-2,2'-diol
97%
- Product Code: 233531
CAS:
877304-22-8
| Molecular Weight: | 618.42 g./mol | Molecular Formula: | C₃₂H₁₂F₁₀O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 535.8±45.0 °C(Predicted) | |
| Density: | 1.575±0.06 g/cm3(Predicted) | Storage Condition: | 2-8°C, Sealed, Inert Gas |
Product Description:
Used as a chiral organocatalyst in asymmetric synthesis, particularly in enantioselective transformations where strong Brønsted acidity and well-defined chiral environment are required. Its perfluorinated aryl groups enhance acidity and stability, making it effective in catalyzing reactions such as asymmetric Friedel-Crafts alkylations, Mannich reactions, and transfer hydrogenations. The rigid binaphthyl backbone provides excellent stereocontrol, allowing high enantioselectivity in the synthesis of pharmaceuticals and fine chemicals. Solubility in fluorinated solvents also enables applications in biphasic and recyclable catalytic systems.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿3,900.00 |
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| 0.250 | 10-20 days | ฿6,620.00 |
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| 1.000 | 10-20 days | ฿17,860.00 |
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(S)-3,3'-Bis(perfluorophenyl)-[1,1'-binaphthalene]-2,2'-diol
Used as a chiral organocatalyst in asymmetric synthesis, particularly in enantioselective transformations where strong Brønsted acidity and well-defined chiral environment are required. Its perfluorinated aryl groups enhance acidity and stability, making it effective in catalyzing reactions such as asymmetric Friedel-Crafts alkylations, Mannich reactions, and transfer hydrogenations. The rigid binaphthyl backbone provides excellent stereocontrol, allowing high enantioselectivity in the synthesis of pharmaceuticals and fine chemicals. Solubility in fluorinated solvents also enables applications in biphasic and recyclable catalytic systems.
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