4-Methoxy-2-(trimethylsilyl)phenyl Trifluoromethanesulfonate
≥95%(GC)
- Product Code: 84217
CAS:
556812-41-0
| Molecular Weight: | 328.38 g./mol | Molecular Formula: | C₁₁H₁₅F₃O₄SSi |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | 1.25 | Storage Condition: | Room temperature, dry, inert gas storage |
Product Description:
This chemical is primarily used as a versatile reagent in organic synthesis, particularly in the formation of carbon-carbon and carbon-heteroatom bonds. It serves as an effective triflating agent, enabling the introduction of the trifluoromethanesulfonate (triflate) group into organic molecules. This group is highly reactive and acts as a leaving group in various substitution reactions, facilitating the synthesis of complex organic compounds. It is especially valuable in the preparation of aryl triflates, which are key intermediates in cross-coupling reactions such as Suzuki, Heck, and Stille couplings. Additionally, its use in the synthesis of pharmaceuticals, agrochemicals, and advanced materials highlights its importance in modern chemical research and industrial applications. The trimethylsilyl group in the structure further enhances its stability and reactivity, making it a preferred choice in demanding synthetic procedures.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿3,429.00 |
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| 1.000 | 10-20 days | ฿8,055.00 |
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4-Methoxy-2-(trimethylsilyl)phenyl Trifluoromethanesulfonate
This chemical is primarily used as a versatile reagent in organic synthesis, particularly in the formation of carbon-carbon and carbon-heteroatom bonds. It serves as an effective triflating agent, enabling the introduction of the trifluoromethanesulfonate (triflate) group into organic molecules. This group is highly reactive and acts as a leaving group in various substitution reactions, facilitating the synthesis of complex organic compounds. It is especially valuable in the preparation of aryl triflates, which are key intermediates in cross-coupling reactions such as Suzuki, Heck, and Stille couplings. Additionally, its use in the synthesis of pharmaceuticals, agrochemicals, and advanced materials highlights its importance in modern chemical research and industrial applications. The trimethylsilyl group in the structure further enhances its stability and reactivity, making it a preferred choice in demanding synthetic procedures.
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