| Identification | Back Directory | [Name]
2H-Indazole-4-carboxamide, N-(1-methylcyclopropyl)-2-(3-pyridinyl)- | [CAS]
1689545-27-4 | [Synonyms]
2H-Indazole-4-carboxamide, N-(1-methylcyclopropyl)-2-(3-pyridinyl)- | [Molecular Formula]
C17H16N4O | [MOL File]
1689545-27-4.mol | [Molecular Weight]
292.34 |
| Hazard Information | Back Directory | [Production Methods]
Public sources do not disclose plant scale manufacturing conditions for indazapyroxamet, however, based on its structure, the molecule is assembled through a multi step construction of the 2H indazole core, beginning with halogenated nitrobenzene precursors that are converted to indazole intermediates via condensation and cyclisation. These intermediates are then functionalised at the 2 position with a 3 pyridyl group and at the 4 position with the N (1 methylcyclopropyl)carboxamide moiety. | [Mechanism of action]
Mode of action involves the modulation of the Transient Receptor Potential Vanilloid (TRPV) channel within the chortodonal organ and causes feeding cessation in piercing/sucking insects | [Pesticide Type]
Insecticide |
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