1-(Trifluoromethanesulfonyl)imidazole
≥98%
- Product Code: 114492
CAS:
29540-81-6
| Molecular Weight: | 200.14 g./mol | Molecular Formula: | C₄H₃F₃N₂O₂S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00037891 | |
| Melting Point: | Boiling Point: | 40°C/10mmHg(lit.) | |
| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is widely used as a reagent in organic synthesis, particularly for introducing the trifluoromethanesulfonyl group into molecules, which is valuable in creating compounds with enhanced stability and reactivity. It is commonly employed in the preparation of pharmaceuticals, agrochemicals, and specialty chemicals, where the triflyl group acts as a strong electron-withdrawing moiety. Additionally, it serves as a key intermediate in the synthesis of complex organic molecules, including heterocycles and biologically active compounds. Its ability to act as a triflating agent makes it useful in cross-coupling reactions, enabling the formation of carbon-carbon and carbon-heteroatom bonds in advanced chemical processes.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | Colorless To Almost Colorless Clear Liquid |
| Purity (%) | 97.5-100 |
| Infrared Spectrum | Conforms To Structure |
| NMR | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.200 | 10-20 days | ฿612.00 |
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| 1.000 | 10-20 days | ฿2,340.00 |
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1-(Trifluoromethanesulfonyl)imidazole
This chemical is widely used as a reagent in organic synthesis, particularly for introducing the trifluoromethanesulfonyl group into molecules, which is valuable in creating compounds with enhanced stability and reactivity. It is commonly employed in the preparation of pharmaceuticals, agrochemicals, and specialty chemicals, where the triflyl group acts as a strong electron-withdrawing moiety. Additionally, it serves as a key intermediate in the synthesis of complex organic molecules, including heterocycles and biologically active compounds. Its ability to act as a triflating agent makes it useful in cross-coupling reactions, enabling the formation of carbon-carbon and carbon-heteroatom bonds in advanced chemical processes.
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