2,2-Dimethyl-4-oxobenzo[1,3]dioxin-5-yl triflate
95%
- Product Code: 83176
CAS:
164014-40-8
| Molecular Weight: | 326.25 g./mol | Molecular Formula: | C₁₁H₉F₃O₆S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09838847 | |
| Melting Point: | 115-117 °C | Boiling Point: | 430.6±45.0 °C(Predicted) |
| Density: | 1.519±0.06 g/cm3(Predicted) | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in organic synthesis as a highly reactive triflate ester, making it a valuable reagent for introducing the 2,2-dimethyl-4-oxobenzo[1,3]dioxin moiety into various molecular frameworks. Its strong electrophilic nature allows it to participate in coupling reactions, particularly in the formation of carbon-carbon and carbon-heteroatom bonds, which are essential in the development of complex organic molecules. It is often employed in the synthesis of pharmaceuticals, agrochemicals, and advanced materials, where precise functionalization is required. Additionally, its stability under certain reaction conditions makes it suitable for use in multi-step synthetic processes, enabling the construction of intricate structures with high selectivity and efficiency.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿7,020.00 |
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| 0.250 | 10-20 days | ฿11,700.00 |
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| 1.000 | 10-20 days | ฿23,400.00 |
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2,2-Dimethyl-4-oxobenzo[1,3]dioxin-5-yl triflate
This chemical is primarily utilized in organic synthesis as a highly reactive triflate ester, making it a valuable reagent for introducing the 2,2-dimethyl-4-oxobenzo[1,3]dioxin moiety into various molecular frameworks. Its strong electrophilic nature allows it to participate in coupling reactions, particularly in the formation of carbon-carbon and carbon-heteroatom bonds, which are essential in the development of complex organic molecules. It is often employed in the synthesis of pharmaceuticals, agrochemicals, and advanced materials, where precise functionalization is required. Additionally, its stability under certain reaction conditions makes it suitable for use in multi-step synthetic processes, enabling the construction of intricate structures with high selectivity and efficiency.
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