1-Trifluoromethyl-1,2-benziodoxol-3(1H)-one
97%
- Product Code: 59058
Alias:
Togni reagent II
CAS:
887144-94-7
Properties:
solid
| Molecular Weight: | 316.02 g./mol | Molecular Formula: | C₈H₄F₃IO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD18800706 | |
| Melting Point: | 158°C | Boiling Point: | |
| Density: | Storage Condition: | 2~8℃, dry, sealed |
Product Description:
This chemical is widely used as a versatile reagent in organic synthesis, particularly for the trifluoromethylation of various compounds. It facilitates the introduction of the trifluoromethyl group into organic molecules, which is valuable in the development of pharmaceuticals, agrochemicals, and materials. Its application is prominent in the synthesis of biologically active molecules, as the trifluoromethyl group often enhances metabolic stability, lipophilicity, and binding affinity. Additionally, it is employed in the preparation of fluorinated building blocks for drug discovery and in the modification of natural products to improve their properties. Its efficiency and selectivity make it a preferred choice in modern synthetic chemistry.
Product Specification:
| Test | Specification |
|---|---|
| Purity | 96.5 100% |
| Appearance | WHITE POWDER OR CRYSTALS |
| Proton NMR spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $45.56 |
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| 5.000 | 10-20 days | $157.80 |
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1-Trifluoromethyl-1,2-benziodoxol-3(1H)-one
This chemical is widely used as a versatile reagent in organic synthesis, particularly for the trifluoromethylation of various compounds. It facilitates the introduction of the trifluoromethyl group into organic molecules, which is valuable in the development of pharmaceuticals, agrochemicals, and materials. Its application is prominent in the synthesis of biologically active molecules, as the trifluoromethyl group often enhances metabolic stability, lipophilicity, and binding affinity. Additionally, it is employed in the preparation of fluorinated building blocks for drug discovery and in the modification of natural products to improve their properties. Its efficiency and selectivity make it a preferred choice in modern synthetic chemistry.
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