| Identification | Back Directory | [Name]
1H-Pyrazole-5-carboxamide, 3-bromo-1-(3-chloro-2-pyridinyl)-N-[4,6-dichloro-3-fluoro-2-[(methylamino)carbonyl]phenyl]- | [CAS]
2129147-03-9 | [Synonyms]
Fluloxandiamide impurity 38
1H-Pyrazole-5-carboxamide, 3-bromo-1-(3-chloro-2-pyridinyl)-N-[4,6-dichloro-3-fluoro-2-[(methylamino)carbonyl]phenyl]- | [Molecular Formula]
C17H10BrCl3FN5O2 | [MOL File]
2129147-03-9.mol | [Molecular Weight]
521.55 |
| Hazard Information | Back Directory | [Production Methods]
The production of fluchlordiniliprole typically begins with assembling the chloro-substituted heterocycle via halogenation or nucleophilic substitution on a pre-functionalised aromatic scaffold under temperature-controlled conditions. In parallel, the anthranilic-acid derivative is converted into an activated acid chloride or equivalent, allowing efficient coupling with the heterocyclic amine or anilide partner. The key amide-forming step is carried out in a polar aprotic solvent with base moderation to suppress over-acylation and side reactions. | [Mechanism of action]
Typically, diamide insecticides work by activating ryanodine receptors, leading to uncontrolled calcium release in insect muscle cells. This causes paralysis and death in target pests. | [Pesticide Type]
Insecticide |
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