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| | Pyridine, 3-ethyl-2-[3-(trifluoromethyl)phenoxy]-6-[3-(trifluoromethyl)-1H-1,2,4-triazol-1-yl]- Basic information |
| | Pyridine, 3-ethyl-2-[3-(trifluoromethyl)phenoxy]-6-[3-(trifluoromethyl)-1H-1,2,4-triazol-1-yl]- Chemical Properties |
| Boiling point | 422.526±55.00 °C(Press: 760.00 Torr)(predicted) | | density | 1.440±0.14 g/cm3(Temp: 25 °C; Press: 760 Torr)(predicted) | | pka | 0.061±0.10(predicted) |
| | Pyridine, 3-ethyl-2-[3-(trifluoromethyl)phenoxy]-6-[3-(trifluoromethyl)-1H-1,2,4-triazol-1-yl]- Usage And Synthesis |
| Production Methods | Flufenazopyr is commercially synthesised through a multi-step process that constructs its complex triazole-based herbicidal structure. The synthesis begins with the formation of a substituted pyridine ring, specifically 3-ethyl-2-(3-trifluoromethylphenoxy)-6-(3-trifluoromethyl-1H-1,2,4-triazol-1-yl)pyridine. This involves coupling reactions between halogenated aromatic compounds and triazole intermediates, incorporating trifluoromethyl groups to enhance herbicidal potency and environmental stability. | | Mechanism of action | Unreported as yet but triazole herbicides typically work by disrupting key enzymatic pathways involved in plant growth and metabolism | | Pesticide Type | Herbicide |
| | Pyridine, 3-ethyl-2-[3-(trifluoromethyl)phenoxy]-6-[3-(trifluoromethyl)-1H-1,2,4-triazol-1-yl]- Preparation Products And Raw materials |
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