| Weight | 359.416 g/mol |
|---|---|
| Formula | C21H23F2NO2 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 4 |
Etoxazole (153233-91-1)
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- Oxidative stress-related and ATPase effects of etoxazole in different tissues of Oreochromis niloticus (Environmental Toxicology and Pharmacology, 2005)
- Mode of action of etoxazole. (Pest Management Science, 2006)
- Genetic basis of resistances to chlorfenapyr and etoxazole in the two-spotted spider mite (Acari: Tetranychidae). (Journal of Economic Entomology, 2002)
- Evaluation of etoxazole toxicity in the liver of Oreochromis niloticus (Pesticide Biochemistry and Physiology, 2004)
- Linkage Between One of the Polygenic Hexythiazox Resistance Genes and an Etoxazole Resistance Gene in the Twospotted Spider Mite (Acari: Tetranychidae) (Journal of Economic Entomology, 2008)
- High resolution genetic mapping uncovers chitin synthase-1 as the target-site of the structurally diverse mite growth inhibitors clofentezine, hexythiazox and etoxazole in Tetranychus urticae (Insect Biochemistry and Molecular Biology, 2014)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H400: Very toxic to aquatic life
Warning Hazardous to the aquatic environment, acute hazard - Category 1 - H410: Very toxic to aquatic life with long lasting effects
Warning Hazardous to the aquatic environment, long-term hazard - Category 1 -
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- Pubchem - Etoxazole
- Wikipedia - etoxazole
Etoxazole is a narrow spectrum systemic acaricide used to combat spider mites. It targets a variety of mites in the egg, larvae and nymph stages however not the adult stage. It also exhibits insecticidal activity towards aphids, the green rice leafhopper and diamondback moth.
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Synthesis
Reactant
+
2-amino-2-(2-ethoxy-4-tert-butylphenyl)ethanol
(Imine formation from aldehyde)
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