R-(-)-1,1'-Bi-2-naphthol Bis(trifluoromethanesulfonate)
98%
- Product Code: 126652
Alias:
(R)-(-)-1,1'-bi-2-naphthol bis(trifluoromethanesulfonate)
CAS:
126613-06-7
| Molecular Weight: | 550.45 g./mol | Molecular Formula: | C₂₂H₁₂F₆O₆S₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00274615 | |
| Melting Point: | 83-85 °C(lit.) | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is widely used as a chiral catalyst in asymmetric synthesis, particularly in enantioselective reactions. It is highly effective in promoting the formation of chiral centers in organic compounds, making it valuable in the production of pharmaceuticals and fine chemicals. Its application extends to catalyzing C-C bond-forming reactions, such as the Mukaiyama aldol reaction and Diels-Alder reactions, where high enantiomeric excess is required. Additionally, it is utilized in the synthesis of complex natural products and bioactive molecules, where precise stereochemical control is critical. Its trifluoromethanesulfonate groups enhance its reactivity and stability, making it a preferred choice in demanding synthetic processes.
Product Specification:
| Test | Specification |
|---|---|
| Melting Point | 82-85 |
| Optical Purity | 0 |
| Purity (%) | 98-100 |
| Specific Rotation [A]20/D(C=1,CHCL3) | 0 |
| Appearance | White To Light Yellow Powder |
| Infrared Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.500 | 10-20 days | £11.08 |
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| 1.000 | 10-20 days | £17.19 |
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| 5.000 | 10-20 days | £66.95 |
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| 25.000 | 10-20 days | £307.14 |
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R-(-)-1,1'-Bi-2-naphthol Bis(trifluoromethanesulfonate)
This chemical is widely used as a chiral catalyst in asymmetric synthesis, particularly in enantioselective reactions. It is highly effective in promoting the formation of chiral centers in organic compounds, making it valuable in the production of pharmaceuticals and fine chemicals. Its application extends to catalyzing C-C bond-forming reactions, such as the Mukaiyama aldol reaction and Diels-Alder reactions, where high enantiomeric excess is required. Additionally, it is utilized in the synthesis of complex natural products and bioactive molecules, where precise stereochemical control is critical. Its trifluoromethanesulfonate groups enhance its reactivity and stability, making it a preferred choice in demanding synthetic processes.
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