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- W2039472004 abstract "This paper reports the synthesis and the biological activity of benzoyl arylureas in which the aryl group bears a trifluoromethyl-substitiited alkyl or alkenyl side chain, R. The activity of these compounds has been evaluated on larvae of S. littoralis, A. aegypti, L. decemlineata and on the eggs of T. urticae. In general: (1) the optimum insecticidal activities are achieved when the substituents on the benzoyl moiety, R1, and R2, are 2,6-difluoro, the substituents on the aryl moiety, R3, are 3,5-dichloro and R1, is 4-(CHC(CI)CF3); (2) the best acaricidal activity is shown when R1, is 2-CI, R2, and R3, are hydrogen atoms and R1, is 4-(CH2CH2CH(CI)CF3); (3) the best overall activity is displayed when R1, is 2-CI, R2 is hydrogen, R3 is 3-chloro and R1 is 4-(CH2CH2CF3)." @default.
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- W2039472004 date "1992-01-01" @default.
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- W2039472004 title "Synthesis and bioactivity of some fluorine-containing benzoyl arylureas. Part I: Insecticidal-acaricidal products in which the aryl group bears a trifluoromethyl-substituted alkyl or alkenyl side chain" @default.
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- W2039472004 doi "https://doi.org/10.1002/ps.2780350207" @default.
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