1,3-Oxathianes with suitable 2- and 5-substituents are highly potent insecticides. In some cases 1,3-oxathiane 3-oxides and 1,3-oxathiane 3,3-dioxides derived by m-chloroperoxybenzoic acid oxidation of the 1,3-oxathianes are even more effective. Housefly LD50s for trans-5(e)-tert-butyl-2(e)-(4-ethynylphenyl)-1,3 oxathiane 3,3-dioxide are 0.3 and 0.03 micrograms/g alone and with piperonyl butoxide, respectively. It is the most insecticidal analogue in the oxathiane series and approaches the potency of (1R)-cis-permethrin.
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书目信息
页码
v.498-502(2)
其它主题
Ensayo biologico; Bioassays; Oxidos; Compuestos heterociclicos; Compose heterocyclique
语言
英语
注释
references. AVAILABILITY: US (DNAL 381 J8223).
类型
Journal Article; Journal Part
来源
Journal-of-agricultural-and-food-chemistry (USA). (Feb 1995). v. 43(2) p. 498-502.
团体作者
Ricerca Inc., Painesville, OH.
Tarbiat Modarres Univ., Tehran (Iran Islamic Republic). College of Medical Sciences.
2012-11-15
AGRIS AP