Ytterbium trifluoromethanesulfonate hydrate
99.9% metals basis
- Product Code: 246134
Alias:
Ytterbium trifluoromethanesulfonate hydrate
CAS:
252976-51-5
| Molecular Weight: | 620.25(anhydrous basis) g./mol | Molecular Formula: | C₃F₉O₉S₃Yb·xH₂O |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03703499 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature |
Product Description:
Widely used as a Lewis acid catalyst in organic synthesis, enabling efficient and selective transformations under mild conditions. It is particularly effective in promoting carbon-carbon and carbon-heteroatom bond-forming reactions, such as Friedel-Crafts acylations, glycosylations, and Diels-Alder reactions. Its water tolerance and stability make it suitable for reactions in aqueous or moist environments, offering advantages over traditional moisture-sensitive catalysts. Additionally, it can be recovered and reused in some processes, supporting greener chemical synthesis. Its unique catalytic activity also extends to polymerization reactions and the activation of carbonyl compounds in aldol and Mannich-type reactions.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 1g | 10-20 days | $43.31 |
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| 5g | 10-20 days | $151.00 |
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Ytterbium trifluoromethanesulfonate hydrate
Widely used as a Lewis acid catalyst in organic synthesis, enabling efficient and selective transformations under mild conditions. It is particularly effective in promoting carbon-carbon and carbon-heteroatom bond-forming reactions, such as Friedel-Crafts acylations, glycosylations, and Diels-Alder reactions. Its water tolerance and stability make it suitable for reactions in aqueous or moist environments, offering advantages over traditional moisture-sensitive catalysts. Additionally, it can be recovered and reused in some processes, supporting greener chemical synthesis. Its unique catalytic activity also extends to polymerization reactions and the activation of carbonyl compounds in aldol and Mannich-type reactions.
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