ChemicalBook--->CAS DataBase List--->1253429-01-4

1253429-01-4

1253429-01-4 Structure

1253429-01-4 Structure
IdentificationBack Directory
[Name]

Z-2-(4-tert-butylphenyl)-2-cyano-1-(1-ethyl-3-methyl-1H-pyrazol-5-yl)eth-1-en-1-yl 2,2-dimethylpropanoate
[CAS]

1253429-01-4
[Synonyms]

Cyetpyrafen
(Z)-2-(4-(Tert-Butyl)phenyl)-2-cyano-1-(1-ethyl-3-methyl-1H-pyrazol-5-yl)vinyl pivalate
E-2-(4-tert-butylphenyl)-2-cyano-1-(1-ethyl-3-methyl-1H-pyrazol-5-yl)eth-1-en-1-yl 2,2-dimethylpropanoate
Z-2-(4-tert-butylphenyl)-2-cyano-1-(1-ethyl-3-methyl-1H-pyrazol-5-yl)eth-1-en-1-yl 2,2-dimethylpropanoate
(1Z)-2-cyano-2-[4-(1,1-dimethylethyl)phenyl]-1-(1-ethyl-3-methyl-1H-pyrazol-5-yl)ethenyl,2,2-dimethyl-Propanoic acid ester
Propanoic acid, 2,2-dimethyl-, (1Z)-2-cyano-2-[4-(1,1-dimethylethyl)phenyl]-1-(1-ethyl-3-methyl-1H-pyrazol-5-yl)ethenyl ester
[Molecular Formula]

C24H31N3O2
[MOL File]

1253429-01-4.mol
[Molecular Weight]

393.52
Chemical PropertiesBack Directory
[Melting point ]

92-93 °C
[Boiling point ]

488.5±45.0 °C(Predicted)
[density ]

1.03±0.1 g/cm3(Predicted)
[pka]

2.08±0.10(Predicted)
Hazard InformationBack Directory
[Description]

Cyetpyrafen is an insecticide and acaricide. Currently little information is available regarding its environmental fate, ecotoxicology or impacts on human health.
[Uses]

Yizuomanjing is used in insecticidal acaricidal synergistic composition and its application.
[Production Methods]

Cyetpyrafen is manufactured through a modular, multi-step synthesis designed to efficiently assemble its characteristic pyrazole-carboxamide scaffold and heavily substituted aromatic system while controlling stereochemistry and halogenated impurities. Industrial routes typically begin with construction of the pyrazole core from a beta dicarbonyl precursor and hydrazine derivative, followed by selective chlorination and introduction of the trifluoromethyl-substituted phenyl ring through either nucleophilic aromatic substitution or metal-catalysed coupling, depending on the producer’s proprietary route. In parallel, the secondary amine fragment is prepared and activated for amide formation. The key step is the coupling of the pyrazole-carboxylic acid (or its acid chloride/mixed anhydride) with the amine under dehydrating conditions that minimise side reactions from the electron-rich heterocycle.
[Mechanism of action]

Absorbed by plant roots. Inhibits mitochondrial electrontransport chain complex II
[Pesticide Type]

Acaricide; Insecticide
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