| Weight | 306.409 g/mol |
|---|---|
| Formula | C20H22N2O |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 3 |
| Rotatable Bonds | 4 |
Fenazaquin (120928-09-8)
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- Fenazaquin Acaricide Specific Binding Sites in NADH: Ubiquinone Oxidoreductase and Apparently the ATP Synthase Stalk (Pesticide Biochemistry and Physiology, 1996)
- Investigation in tea on fate of fenazaquin residue and its transfer in brew. (Food and Chemical Toxicology, 2004)
- Resistance to fenazaquin and tebufenpyrad in Panonychus ulmi Koch (Acari: Tetranychidae) populations from South of France apple orchards (Crop Protection, 2003)
- Resistance mechanisms to fenazaquin in Iranian populations of two-spotted spider mite, Tetranychus urticae Koch (Acari: Tetranychidae) (International Journal of Acarology, 2012)
- Sublethal effects of fenazaquin on life table parameters of the predatory mite Amblyseius swirskii (Acari: Phytoseiidae) (Experimental and Applied Acarology, 2014)
- Fenazaquin, a selective acaricide for use in IPM in apple in the UK (Crop Protection, 1993)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H301: Toxic if swallowed
Danger Acute toxicity, oral - Category 3 - 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 -
SMILESCC(C)(C)C1=CC=C(C=C1)CCOC2=NC=NC3=CC=CC=C32
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InChIKeyDMYHGDXADUDKCQ-UHFFFAOYSA-N
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CID 5320866
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Reactant
(Williamson ether)
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