| Identification | Back Directory | [Name]
Pyridine, 3-ethyl-2-[3-(trifluoromethyl)phenoxy]-6-[3-(trifluoromethyl)-1H-1,2,4-triazol-1-yl]- | [CAS]
3052252-60-2 | [Synonyms]
Pyridine, 3-ethyl-2-[3-(trifluoromethyl)phenoxy]-6-[3-(trifluoromethyl)-1H-1,2,4-triazol-1-yl]- | [Molecular Formula]
C17H12F6N4O | [MOL File]
3052252-60-2.mol | [Molecular Weight]
402.29 |
| Chemical Properties | Back Directory | [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) |
| Hazard Information | Back Directory | [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 |
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