1,1,1-Trifluoromethanesulfonic acid 2-(1,3-dihydro-1,3-dioxo-2H-benz[f]isoindol-2-yl)ethyl ester
90%
- Product Code: 62374
CAS:
128651-50-3
| Molecular Weight: | 373.30 g./mol | Molecular Formula: | C₁₅H₁₀F₃NO₅S |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20°C |
Product Description:
This chemical is primarily used as a highly reactive intermediate in organic synthesis, particularly in the development of pharmaceuticals and specialty chemicals. Its strong electrophilic properties make it valuable for introducing trifluoromethanesulfonate (triflate) groups into molecules, which can enhance reactivity in subsequent reactions. It is often employed in cross-coupling reactions, such as Suzuki or Heck reactions, where it acts as a leaving group to facilitate the formation of carbon-carbon bonds. Additionally, it is utilized in the synthesis of complex organic compounds, including natural products and polymers, due to its ability to activate specific functional groups. Its application in medicinal chemistry is notable for creating bioactive molecules with potential therapeutic effects.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to Off-White Solid, Powder, or Crystals |
| PURITY | 89.5-100 |
| Proton NMR spectrum | Conforms to Structure |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.025 | 10-20 days | ฿8,622.00 |
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1,1,1-Trifluoromethanesulfonic acid 2-(1,3-dihydro-1,3-dioxo-2H-benz[f]isoindol-2-yl)ethyl ester
This chemical is primarily used as a highly reactive intermediate in organic synthesis, particularly in the development of pharmaceuticals and specialty chemicals. Its strong electrophilic properties make it valuable for introducing trifluoromethanesulfonate (triflate) groups into molecules, which can enhance reactivity in subsequent reactions. It is often employed in cross-coupling reactions, such as Suzuki or Heck reactions, where it acts as a leaving group to facilitate the formation of carbon-carbon bonds. Additionally, it is utilized in the synthesis of complex organic compounds, including natural products and polymers, due to its ability to activate specific functional groups. Its application in medicinal chemistry is notable for creating bioactive molecules with potential therapeutic effects.
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