3-Pyridyl Trifluoromethanesulfonate
≥98%
- Product Code: 117620
CAS:
107658-27-5
| Molecular Weight: | 227.16 g./mol | Molecular Formula: | C₆H₄F₃NO₃S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00799579 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
3-Pyridyl trifluoromethanesulfonate is primarily used as a versatile reagent in organic synthesis, particularly in the formation of carbon-nitrogen bonds. It serves as an effective electrophile in cross-coupling reactions, enabling the introduction of pyridyl groups into various organic compounds. This chemical is valuable in pharmaceutical research for the development of drug candidates, as the pyridyl moiety is a common structural feature in many bioactive molecules. Additionally, it is employed in the synthesis of agrochemicals and materials science, where the incorporation of pyridyl groups can enhance the properties of the final product. Its reactivity and stability make it a useful tool for chemists in constructing complex molecular architectures.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | Colorless To Red To Green Clear Liquid |
| Purity (%) | 98 |
| Infrared Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $113.51 |
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| 5.000 | 10-20 days | $321.45 |
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3-Pyridyl Trifluoromethanesulfonate
3-Pyridyl trifluoromethanesulfonate is primarily used as a versatile reagent in organic synthesis, particularly in the formation of carbon-nitrogen bonds. It serves as an effective electrophile in cross-coupling reactions, enabling the introduction of pyridyl groups into various organic compounds. This chemical is valuable in pharmaceutical research for the development of drug candidates, as the pyridyl moiety is a common structural feature in many bioactive molecules. Additionally, it is employed in the synthesis of agrochemicals and materials science, where the incorporation of pyridyl groups can enhance the properties of the final product. Its reactivity and stability make it a useful tool for chemists in constructing complex molecular architectures.
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