Trifluoromethanesulfonyl chloride
99%
- Product Code: 121855
Alias:
Trifluoromethanesulfonyl chloride
CAS:
421-83-0
| Molecular Weight: | 168.52 g./mol | Molecular Formula: | CF₃SO₂Cl |
|---|---|---|---|
| EC Number: | 207-009-0 | MDL Number: | MFCD00007451 |
| Melting Point: | Boiling Point: | 29-32 °C(lit.) | |
| Density: | 1.583 g/mL at 25 °C(lit.) | Storage Condition: | -20°C |
Product Description:
Trifluoromethanesulfonyl chloride is widely used in organic synthesis as a powerful reagent for introducing the trifluoromethanesulfonyl (triflyl) group into molecules. It is particularly valuable in the preparation of triflates, which are highly reactive intermediates in various chemical reactions, including cross-coupling reactions, nucleophilic substitutions, and polymerizations. The compound is also employed in the synthesis of pharmaceuticals and agrochemicals, where the triflyl group enhances the stability and reactivity of the target molecules. Additionally, it serves as a catalyst or co-catalyst in certain organic transformations, such as Friedel-Crafts acylation and esterification reactions, due to its strong electrophilic nature. Its applications extend to the field of materials science, where it is used to modify polymers and create specialized coatings with unique properties.
Product Specification:
| Test | Specification |
|---|---|
| Purity (%) | 99-100 |
| Refractive Index N20/D | 1.332-1.338 |
| Appearance | Colorless To Light Yellow Liquid |
| Infrared Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿600.00 |
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| 5.000 | 10-20 days | ฿1,460.00 |
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| 25.000 | 10-20 days | ฿4,780.00 |
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| 100.000 | 10-20 days | ฿15,480.00 |
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| 500.000 | 10-20 days | ฿69,690.00 |
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Trifluoromethanesulfonyl chloride
Trifluoromethanesulfonyl chloride is widely used in organic synthesis as a powerful reagent for introducing the trifluoromethanesulfonyl (triflyl) group into molecules. It is particularly valuable in the preparation of triflates, which are highly reactive intermediates in various chemical reactions, including cross-coupling reactions, nucleophilic substitutions, and polymerizations. The compound is also employed in the synthesis of pharmaceuticals and agrochemicals, where the triflyl group enhances the stability and reactivity of the target molecules. Additionally, it serves as a catalyst or co-catalyst in certain organic transformations, such as Friedel-Crafts acylation and esterification reactions, due to its strong electrophilic nature. Its applications extend to the field of materials science, where it is used to modify polymers and create specialized coatings with unique properties.
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