Weight | 488.771 g/mol |
---|---|
Formula | C21H11ClF6N2O3 |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 2 |
Aromatic Rings | 3 |
Rotatable Bonds | 4 |
Flufenoxuron (101463-69-8)
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- The inhibition of chitin synthesis in spodoptera littoralis larvae by flufenoxuron, teflubenzuron and diflubenzuron (Pesticide Science, 1990)
- Degradation of the acaricides abamectin, flufenoxuron and amitraz on Saudi Arabian dates (Food Chemistry, 2007)
- Flufenoxuron, an acylurea insect growth regulator, alters development of Tribolium castaneum (Herbst) (Coleoptera: Tenebrionidae) by modulating levels of chitin, soluble protein content, and HSP70 and p34cdc2 in the larval tissues (Pesticide Biochemistry and Physiology, 2006)
- Development of a compound-specific ELISA for flufenoxuron and an improved class-specific assay for benzoylphenylurea insect growth regulators. (Journal of Agricultural and Food Chemistry, 1999)
- Cytochemical demonstration of the effects of the acylureas flufenoxuron and diflubenzuron on the incorporation of chitin into insect cuticle (Pesticide Science, 1990)
- Compatibility of the entomopathogenic fungus Beauveria bassiana with flufenoxuron and azadirachtin against Tetranychus urticae (Experimental and Applied Acarology, 2012)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H362: May cause harm to breast-fed children
- H410: Very toxic to aquatic life with long lasting effects
Warning Hazardous to the aquatic environment, long-term hazard - Category 1 -
SMILESC1=CC(=C(C(=C1)F)C(=O)NC(=O)NC2=C(C=C(C=C2)OC3=C(C=C(C=C3)C(F)(F)F)Cl)F)F
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101463-63-2
(Thiourea)
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