Tin(II) trifluoromethanesulfonate
98%
- Product Code: 68357
Alias:
Tin trifluoromethanesulfonate
CAS:
62086-04-8
| Molecular Weight: | 416.85 g./mol | Molecular Formula: | C₂F₆O₆S₂Sn |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00191251 | |
| Melting Point: | ≥300 °C(lit.) | Boiling Point: | |
| Density: | Storage Condition: | 2-8 °C, dry, sealed |
Product Description:
Tin(II) trifluoromethanesulfonate is widely used as a catalyst in organic synthesis due to its strong Lewis acid properties. It is particularly effective in promoting various reactions such as Friedel-Crafts alkylations, acylations, and cyclizations. Its ability to activate carbonyl compounds makes it valuable in the synthesis of complex organic molecules, including natural products and pharmaceuticals. Additionally, it is employed in polymerization processes, where it helps initiate the formation of specific polymers with desired properties. The compound’s stability and solubility in organic solvents further enhance its utility in diverse chemical transformations.
Product Specification:
| Test | Specification |
|---|---|
| PURITYTITRATION | 97.5 102.5% |
| APPEARANCE | White to off-white powder,crystals and/or chunks |
| INFRARED SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿300.00 |
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| 5.000 | 10-20 days | ฿670.00 |
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| 25.000 | 10-20 days | ฿3,200.00 |
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Tin(II) trifluoromethanesulfonate
Tin(II) trifluoromethanesulfonate is widely used as a catalyst in organic synthesis due to its strong Lewis acid properties. It is particularly effective in promoting various reactions such as Friedel-Crafts alkylations, acylations, and cyclizations. Its ability to activate carbonyl compounds makes it valuable in the synthesis of complex organic molecules, including natural products and pharmaceuticals. Additionally, it is employed in polymerization processes, where it helps initiate the formation of specific polymers with desired properties. The compound’s stability and solubility in organic solvents further enhance its utility in diverse chemical transformations.
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