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| | TRIFLUOROMETHYL SULFINYL CHLORIDE Basic information |
| Product Name: | TRIFLUOROMETHYL SULFINYL CHLORIDE | | Synonyms: | TRIFLUOROMETHYL SULFINYL CHLORIDE;Methanesulfinylchloride, 1,1,1-trifluoro-;TrifluoroMethanesulfinyl chloride;1,1,1-Trifluoromethanesulfinyl chloride;trifluoromethyl sulfacyl chloride;rifluoromethanesulfinylchloride | | CAS: | 20621-29-8 | | MF: | CClF3OS | | MW: | 152.52 | | EINECS: | | | Product Categories: | | | Mol File: | 20621-29-8.mol |  |
| | TRIFLUOROMETHYL SULFINYL CHLORIDE Chemical Properties |
| Boiling point | 149.4±35.0 °C(Predicted) | | density | 1.852±0.06 g/cm3(Predicted) | | solubility | soluble in No data available |
| | TRIFLUOROMETHYL SULFINYL CHLORIDE Usage And Synthesis |
| Chemical Properties | This product is liquid, bp30 ℃, volatile at room temperature, soluble in inert organic solvent, and decomposes in contact with water. | | Uses | Trifluoromethyl sulfinyl chloride is an intermediate for the insecticide fipronil. | | Synthesis | The preparation method of Trifluoromethyl sulfinyl chloride is that CF3Cl is reacted with sodium dithionite to generate sodium trifluoromethyl sulfite, and then reacted with thionyl chloride to generate a product. Reaction equation: CF3Cl1+Na2S2O4→CF3SO2Na[SOCl2]→CF3SOCl
It can also be reacted with potassium trifluoroacetate and sulfur dioxide in a solvent to generate Potassium trifluoromethyl sulfoxide, and then react with thionyl chloride to produce the product. Reaction equation: CF3COOK+SO2→CF3SO2K→CF3< /SUB>SOCl |
| | TRIFLUOROMETHYL SULFINYL CHLORIDE Preparation Products And Raw materials |
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