Pentafluorophenyl Trifluoromethanesulfonate
≥97%
- Product Code: 121851
CAS:
60129-85-3
| Molecular Weight: | 316.12 g./mol | Molecular Formula: | C₇F₈O₃S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD07784319 | |
| Melting Point: | Boiling Point: | 40°C/0.5mmHg(lit.) | |
| Density: | Storage Condition: | room temperature |
Product Description:
Pentafluorophenyl trifluoromethanesulfonate is widely used as a highly reactive reagent in organic synthesis, particularly in the introduction of the pentafluorophenyl group into various molecules. Its strong electrophilic nature makes it valuable in the formation of carbon-carbon and carbon-heteroatom bonds, often employed in the synthesis of complex organic compounds, including pharmaceuticals and agrochemicals. Additionally, it serves as a key intermediate in the preparation of specialty chemicals and materials, such as polymers and liquid crystals, where the pentafluorophenyl group imparts unique properties like thermal stability and chemical resistance. Its application extends to peptide chemistry, where it is used for selective modifications and protecting group strategies, enhancing the efficiency of synthetic routes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.200 | 10-20 days | ฿3,990.00 |
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Pentafluorophenyl Trifluoromethanesulfonate
Pentafluorophenyl trifluoromethanesulfonate is widely used as a highly reactive reagent in organic synthesis, particularly in the introduction of the pentafluorophenyl group into various molecules. Its strong electrophilic nature makes it valuable in the formation of carbon-carbon and carbon-heteroatom bonds, often employed in the synthesis of complex organic compounds, including pharmaceuticals and agrochemicals. Additionally, it serves as a key intermediate in the preparation of specialty chemicals and materials, such as polymers and liquid crystals, where the pentafluorophenyl group imparts unique properties like thermal stability and chemical resistance. Its application extends to peptide chemistry, where it is used for selective modifications and protecting group strategies, enhancing the efficiency of synthetic routes.
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