Trimethylsilyl trifluoromethanesulfonate
98.0%
- Product Code: 88309
Alias:
Trimethylsilyl trifluoromethanesulfonate; Trimethylsilyl trifluoromethanesulfonate
CAS:
27607-77-8
| Molecular Weight: | 222.26 g./mol | Molecular Formula: | C₄H₉F₃SiSO₃ |
|---|---|---|---|
| EC Number: | 248-565-4 | MDL Number: | MFCD00000406 |
| Melting Point: | Boiling Point: | 77 °C/80 mmHg(lit.) | |
| Density: | 1.228 g/mL at 25 °C | Storage Condition: | 2~8°C |
Product Description:
Trimethylsilyl trifluoromethanesulfonate is widely used in organic synthesis as a powerful silylating agent and catalyst. It is particularly effective in promoting the formation of silyl ethers from alcohols, which are useful protecting groups in multi-step synthesis. Additionally, it is employed in the activation of glycosyl donors in carbohydrate chemistry, facilitating the synthesis of complex sugars and glycoconjugates. Its strong Lewis acid properties make it valuable in Friedel-Crafts acylation and alkylation reactions, enabling the construction of carbon-carbon bonds. In peptide chemistry, it aids in the removal of protecting groups and the activation of carboxylic acids for amide bond formation. Its versatility and reactivity make it a key reagent in the development of pharmaceuticals, agrochemicals, and advanced materials.
Product Specification:
| Test | Specification |
|---|---|
| PURITYNEUTRALIZATION TITRATION | 98 100% |
| REFRACTIVE INDEX N20D | 1.359-1.361 |
| APPEARANCE | Colorless to light yellow liquid |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 10.000 | 10-20 days | ฿390.00 |
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| 25.000 | 10-20 days | ฿580.00 |
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| 50.000 | 10-20 days | ฿1,260.00 |
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| 250.000 | 10-20 days | ฿5,690.00 |
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Trimethylsilyl trifluoromethanesulfonate
Trimethylsilyl trifluoromethanesulfonate is widely used in organic synthesis as a powerful silylating agent and catalyst. It is particularly effective in promoting the formation of silyl ethers from alcohols, which are useful protecting groups in multi-step synthesis. Additionally, it is employed in the activation of glycosyl donors in carbohydrate chemistry, facilitating the synthesis of complex sugars and glycoconjugates. Its strong Lewis acid properties make it valuable in Friedel-Crafts acylation and alkylation reactions, enabling the construction of carbon-carbon bonds. In peptide chemistry, it aids in the removal of protecting groups and the activation of carboxylic acids for amide bond formation. Its versatility and reactivity make it a key reagent in the development of pharmaceuticals, agrochemicals, and advanced materials.
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