（ＲＳ）－α－シアノ－３－フェノキシベンジル２，２，３，３－テトラメチルシクロプロパンカルボキシラート

（ＲＳ）－α－シアノ－３－フェノキシベンジル２，２，３，３－テトラメチルシクロプロパンカルボキシラート 化学特性,用途語,生産方法

• 使用

  Fenpropathrin controls many species of mites and insects on pome fruit, citrus, vines, hops, vegetables, cotton, ornamentals and glasshouse crops such as tomatoes.

• 代謝経路

  Fenpropathrin possesses only one chiral centre (at benzylic carbon) and therefore presents a much simpler stereochemical picture than that seen with most of the other pyrethroids. Most metabolic work has been conducted with the RS racemate. Solution and surface photochemistry, and degradation in water, soils, plants and animals, have been reported. The fate of the 3-phenoxybenzyl portion of the molecule is very similar to that reported for cypermethrin and other analogues. Degradation is mainly by ester cleavage and hydroxylation.

（ＲＳ）－α－シアノ－３－フェノキシベンジル２，２，３，３－テトラメチルシクロプロパンカルボキシラート 上流と下流の製品情報

64257-84-7, （ＲＳ）－α－シアノ－３－フェノキシベンジル２，２，３，３－テトラメチルシクロプロパンカルボキシラート キーワード