[(Oxido)phenyl(trifluoromethyl)-λ4-sulfanylidene]dimethylammonium Tetrafluoroborate
≥98%
- Product Code: 79635
CAS:
1046786-08-6
| Molecular Weight: | 325.05 g./mol | Molecular Formula: | C₉H₁₁BF₇NOS |
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| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized as a highly effective reagent in organic synthesis, particularly in the field of electrophilic trifluoromethylation. It enables the introduction of the trifluoromethyl group into various organic molecules, which is a crucial modification in the development of pharmaceuticals, agrochemicals, and materials science. The reagent is valued for its ability to react with a wide range of nucleophiles, including enolates, amines, and heteroaromatic compounds, facilitating the creation of complex molecules with enhanced properties such as increased metabolic stability, lipophilicity, and bioavailability. Its application is especially significant in the synthesis of active pharmaceutical ingredients (APIs) where the trifluoromethyl group plays a key role in improving drug efficacy and selectivity. Additionally, it is employed in the preparation of advanced materials, where the introduction of fluorine atoms can impart unique electronic, thermal, and chemical resistance properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.200 | 10-20 days | $229.63 |
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[(Oxido)phenyl(trifluoromethyl)-λ4-sulfanylidene]dimethylammonium Tetrafluoroborate
This chemical is primarily utilized as a highly effective reagent in organic synthesis, particularly in the field of electrophilic trifluoromethylation. It enables the introduction of the trifluoromethyl group into various organic molecules, which is a crucial modification in the development of pharmaceuticals, agrochemicals, and materials science. The reagent is valued for its ability to react with a wide range of nucleophiles, including enolates, amines, and heteroaromatic compounds, facilitating the creation of complex molecules with enhanced properties such as increased metabolic stability, lipophilicity, and bioavailability. Its application is especially significant in the synthesis of active pharmaceutical ingredients (APIs) where the trifluoromethyl group plays a key role in improving drug efficacy and selectivity. Additionally, it is employed in the preparation of advanced materials, where the introduction of fluorine atoms can impart unique electronic, thermal, and chemical resistance properties.
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