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| | 2-Pyridinecarboxylic acid, 4-amino-3-chloro-5-fluoro-6-(7-fluoro-1H-indol-6-yl)-, cyanomethyl ester Basic information |
| | 2-Pyridinecarboxylic acid, 4-amino-3-chloro-5-fluoro-6-(7-fluoro-1H-indol-6-yl)-, cyanomethyl ester Chemical Properties |
| Boiling point | 658.1±55.0 °C(Predicted) | | density | 1.571±0.06 g/cm3(Predicted) | | pka | 13.20±0.30(Predicted) |
| | 2-Pyridinecarboxylic acid, 4-amino-3-chloro-5-fluoro-6-(7-fluoro-1H-indol-6-yl)-, cyanomethyl ester Usage And Synthesis |
| Production Methods | The commercial production process of indolauxipyr cyanomethyl is not available in open literature. However, based on its structure, its production process would probably begin with the preparation of the substituted indole or indole carboxylic acid precursor. Next an auxinic aryl oxy or heteroaryl oxy linkage would be introduced through nucleophilic aromatic substitution or ester formation. Finally, the cyanomethyl group is attached using a halomethyl nitrile or activated cyanomethylating reagent under controlled conditions. Purification and crystallisation of the technical material would complete the process. | | Mechanism of action | Synthetic auxin, It causes uncontrolled cell division and elongation, ultimately causing plant death in targeted weeds. | | Pesticide Type | Herbicide |
| | 2-Pyridinecarboxylic acid, 4-amino-3-chloro-5-fluoro-6-(7-fluoro-1H-indol-6-yl)-, cyanomethyl ester Preparation Products And Raw materials |
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