| Weight | 421.497 g/mol |
|---|---|
| Formula | C24H27N3O4 |
| Hydrogen Acceptors | 7 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 3 |
| Rotatable Bonds | 7 |
Fenpyroximate (111812-58-9)
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- The ND5 subunit was labeled by a photoaffinity analogue of fenpyroximate in bovine mitochondrial complex I. (Biochemistry, 2003)
- Fenpyroximate resistance in Tetranychus urticae (Acari: Tetranychidae): cross-resistance and biochemical resistance mechanisms. (Pest Management Science, 2004)
- Effect of a new acaricide, fenpyroximate, on energy metabolism and mitochondrial morphology in adult female Tetranychus urticae (two-spotted spider mite) (Pesticide Biochemistry and Physiology, 1992)
- Selections for fenpyroximate resistance and susceptibility, and inheritance, cross-resistance and stability of fenpyroximate resistance in Tetranychus urticae Koch (Acari: Tetranychidae) (Applied Entomology and Zoology, 2004)
- Residual and sublethal effects of fenpyroximate and pyridaben on the instantaneous rate of increase of Tetranychus urticae (Crop Protection, 2006)
- Species-Specific Detoxification Metabolism of Fenpyroximate, a Potent Acaricide (Pesticide Biochemistry and Physiology, 2000)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC1=NN(C(=C1C=NOCC2=CC=C(C=C2)C(=O)OC(C)(C)C)OC3=CC=CC=C3)C
-
InChIKeyYYJNOYZRYGDPNH-UHFFFAOYSA-N
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Synthesis
1,3-dimethyl-5-phenoxy-1H-pyrazole-4-carbaldehyde
+
Reactant
(Imine formation from aldehyde)
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