|
|
| | Methyl 2-[[[4-chloro-2-fluoro-5-[(2,2,2-trifluoroethyl)thio]phenyl]amino]methyl]benzoate Basic information |
| | Methyl 2-[[[4-chloro-2-fluoro-5-[(2,2,2-trifluoroethyl)thio]phenyl]amino]methyl]benzoate Chemical Properties |
| Boiling point | 464.4±45.0 °C(Predicted) | | density | 1.42±0.1 g/cm3(Temp: 20 °C; Press: 760 Torr)(Predicted) | | pka | 1.13±0.50(Predicted) |
| | Methyl 2-[[[4-chloro-2-fluoro-5-[(2,2,2-trifluoroethyl)thio]phenyl]amino]methyl]benzoate Usage And Synthesis |
| Production Methods | Bentioflumin is produced through a multi-step synthesis that constructs its benzamide-based acaricide framework. The process begins with the preparation of a substituted aniline derivative containing chloro, fluoro, and trifluoroethylthio substituents on the aromatic ring. This intermediate is then coupled via nucleophilic substitution with a benzylamine fragment to introduce the aminomethyl linkage. Finally, esterification with methanol yields the methyl benzoate moiety, completing the structure. Careful control of reaction conditions ensures the correct substitution pattern and stability of the trifluoroethylthio group, after which the product is purified and formulated for agricultural use. | | Mechanism of action | Acts as a mitochondrial electron transport inhibitor, specifically targeting complex II (succinate dehydrogenase) in mites. By disrupting energy production in the mitochondria, it causes rapid paralysis and death of target species. | | Pesticide Type | Acaricide; Insecticide |
| | Methyl 2-[[[4-chloro-2-fluoro-5-[(2,2,2-trifluoroethyl)thio]phenyl]amino]methyl]benzoate Preparation Products And Raw materials |
|