Yttrium(III) trifluoromethanesulfonate
98%
- Product Code: 105700
Alias:
Yttrium trifluoromethanesulfonate
CAS:
52093-30-8
| Molecular Weight: | 536.11 g./mol | Molecular Formula: | C₃F₉O₉S₃Y |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00209623 | |
| Melting Point: | Boiling Point: | ||
| Density: | 1.7 | Storage Condition: | room temperature |
Product Description:
Yttrium(III) trifluoromethanesulfonate is widely used as a Lewis acid catalyst in organic synthesis due to its strong electrophilic properties. It is particularly effective in promoting various reactions such as Friedel-Crafts acylation, aldol condensation, and Diels-Alder reactions. Its ability to activate carbonyl compounds makes it valuable in the synthesis of complex organic molecules, including pharmaceuticals and fine chemicals. Additionally, it is employed in polymerization processes, where it enhances the rate and selectivity of the reaction. The compound's stability in aqueous and organic solvents further broadens its applicability in diverse chemical environments.
Product Specification:
| Test | Specification |
|---|---|
| Purity (Titration) | 98-100 |
| Appearance | White To Off-White Solid, Powder, Or Crystals |
| Infrared Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿360.00 |
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| 5.000 | 10-20 days | ฿800.00 |
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| 25.000 | 10-20 days | ฿3,790.00 |
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| 100.000 | 10-20 days | ฿15,130.00 |
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Yttrium(III) trifluoromethanesulfonate
Yttrium(III) trifluoromethanesulfonate is widely used as a Lewis acid catalyst in organic synthesis due to its strong electrophilic properties. It is particularly effective in promoting various reactions such as Friedel-Crafts acylation, aldol condensation, and Diels-Alder reactions. Its ability to activate carbonyl compounds makes it valuable in the synthesis of complex organic molecules, including pharmaceuticals and fine chemicals. Additionally, it is employed in polymerization processes, where it enhances the rate and selectivity of the reaction. The compound's stability in aqueous and organic solvents further broadens its applicability in diverse chemical environments.
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