4-(Trifluoromethylsulfonyl)benzonitrile
≥97%
- Product Code: 244737
CAS:
312-21-0
| Molecular Weight: | 235.18 g./mol | Molecular Formula: | C₈H₄F₃NO₂S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01631631 | |
| Melting Point: | 87-92 °C | Boiling Point: | |
| Density: | Storage Condition: | Room temperature, seal, dry |
Product Description:
Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals due to the presence of both nitrile and trifluoromethylsulfonyl functional groups, which are key in forming biologically active molecules. The compound is particularly valuable in cross-coupling reactions, such as Suzuki and Heck reactions, where the trifluoromethylsulfonyl group acts as a good leaving group, enabling the formation of carbon-carbon bonds. It is also employed in the preparation of liquid crystals and organic electronic materials, where its electron-withdrawing properties help modulate the electronic characteristics of the final product. Its stability and reactivity profile make it suitable for use in mild reaction conditions, enhancing its utility in complex multi-step syntheses.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿3,900.00 |
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4-(Trifluoromethylsulfonyl)benzonitrile
Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals due to the presence of both nitrile and trifluoromethylsulfonyl functional groups, which are key in forming biologically active molecules. The compound is particularly valuable in cross-coupling reactions, such as Suzuki and Heck reactions, where the trifluoromethylsulfonyl group acts as a good leaving group, enabling the formation of carbon-carbon bonds. It is also employed in the preparation of liquid crystals and organic electronic materials, where its electron-withdrawing properties help modulate the electronic characteristics of the final product. Its stability and reactivity profile make it suitable for use in mild reaction conditions, enhancing its utility in complex multi-step syntheses.
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