Two series of novel 2,4-diphenyl-1,3-oxazolines containing an oxime ether moiety were designed and synthesized via the key intermediate N-(2-chloro-1-(p-tolyl)ethyl)-2,6-difluorobenzamide. The bioassay results showed that the target compounds with an oxime ether substituent at the para position of 4-phenyl exhibited excellent acaricidal activity against Tetranychus cinnabarinus in the laboratory. Moreover, all of the target compounds had much higher activities than etoxazole, as the ovicidal and larvicidal activities of the target compounds I-a-I-l and II-a-II-n against T. cinnabarinus were all over 90% at 0.001 mg L, but etoxazole gave only 30% and 40% respectively at the same concentration. The activity order of compounds with regard to acaricidal activity in vivo was almost consistent with their affinity activity with sulfonylurea receptor (SUR) of Blattella germanica in vitro, hence, it was supposed that the acaricidal mechanism of action of the target compounds was that they can bind with the site of SUR and therefore inhibit chitin synthesis. Moreover, the eminent effect of the compound II-l, [2-(trifluoromethyl)benzaldehyde O-(4-(2-(2,6-difluorophenyl)-4,5-dihydrooxazol-4-yl)benzyl) oxime], against Panonychus citri and T. cinnabarinus in the field indicated that II-l exhibited a promising application prospect as a new candicate for controlling spider mites in the field.

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Etoxazole, 2-(2,6-difluorophenyl-4-[4-(1,1-dimethylethyl)-2-ethoxy-phenyl]-4,5-dihydrooxazole, an organofluorine chitin synthesis inhibitor, was assayed for its bioactivities against several major insect and acarus pests and compared to several other pesticides: two chitin synthesis inhibitors, hexaflumuron and chlorfluazuron; a pyrethroid, permethrin; an organophosphate, acephate; a carboximide, hexythiazox; and a tetrazine, clofentezine. The LC 50 of etoxazole was calculated using probit analysis of the concentration-dependent mortality data against susceptible and resistant strains of the beet armyworm, Spodoptera exigua (Hubner) (Lepidoptera: Noctuidae); diamondback moth, Plutella xylostella L. (Plutellidae); bean aphid, Aphis craccivora Koch (Hemiptera: Aphididae); and carmine spider mite, Tetranychus cinnabarinus (Boisduval) Boudreaux (Trombidiformes: Tetranychidae). The resistant strains were found to be resistant against all tested pesticides except etoxazole. The bioactivity of etoxazole was many times that of the other tested insecticides and acaricides widely used in vegetable crops in China. On the basis of our research, etoxazole can be expected to be extensively used on vegetable crops in China.

Etoxazole, 2-(2,6-difluorophenyl-4-[4-(1,1-dimethylethyl)-2-ethoxy-phenyl]-4,5-dihydrooxazole, an organofluorine chitin synthesis inhibitor, was assayed for its bioactivities against several major insect and acarus pests and compared to several other pesticides: two chitin synthesis inhibitors, hexaflumuron and chlorfluazuron; a pyrethroid, permethrin; an organophosphate, acephate; a carboximide, hexythiazox; and a tetrazine, clofentezine. The LC 50 of etoxazole was calculated using probit analysis of the concentration-dependent mortality data against susceptible and resistant strains of the beet armyworm, Spodoptera exigua (Hubner) (Lepidoptera: Noctuidae); diamondback moth, Plutella xylostella L. (Plutellidae); bean aphid, Aphis craccivora Koch (Hemiptera: Aphididae); and carmine spider mite, Tetranychus cinnabarinus (Boisduval) Boudreaux (Trombidiformes: Tetranychidae). The resistant strains were found to be resistant against all tested pesticides except etoxazole. The bioactivity of etoxazole was many times that of the other tested insecticides and acaricides widely used in vegetable crops in China. On the basis of our research, etoxazole can be expected to be extensively used on vegetable crops in China.