178043-46-4

Upstream product

• 110-52-1 1,4-dibromo-butane 
• 178043-12-4 4-(3,3-dichloro-2-propenyloxy)-2,6-dichlorophenol 
• 178043-37-3 4-((3,3-dichloroallyl)oxy)phenol 
• 870534-16-0 4-[4-(3,3-dichloroprop-2-enyloxy)-2,6-dichlorophenoxy]butyl acetate 
• 870534-14-8 4-[2,6-dichloro-4-(phenylmethoxy)phenoxy]butyl acetate 
• 870534-15-9 4-(2,6-dichloro-4-hydroxyphenoxy)butyl acetate 
• 155916-12-4 2,6-dichloro-4-benzyloxyphenol 

Relevant academic research and scientific papers

Design, synthesis and bioactivities of novel dichloro-allyloxy-phenol-containing pyrazole oxime derivatives

In this study, in order to find novel biologically active pyrazole oxime compounds, a number of dichloro-allyloxy-phenol-containing pyrazole oximes were designed and synthesized according to the method of active group combination. All of the target compounds were confirmed by 1H-NMR, 13C-NMR and elemental analysis. In addition, bioassays showed that all of the newly synthesized compounds had no acaricidal activity against Tetranychus cinnabarinus and low insecticidal activity against Aphis craccivora at tested concentrations. However, most of them displayed excellent insecticidal activity against Oriental armyworm at a concentration of 500 μg/mL, and some designed compounds still exhibited potent insecticidal activity against Oriental armyworm even at the dose of 20 μg/mL, especially compounds 7f, 7n and 7p had 100%, 90% and 90% inhibition rates, respectively, which were comparable to that of the control pyridalyl.

SUBSTITUTED CYCLIC UREA DERIVATIVES

Certain novel phenyl substituted cyclic urea derivatives have unexpected insecticidal activity. These compounds are represented by formula I: where A, B a, D, b, E, G, c, d, J, X and R through R10, inclusively, are fully described herein. In ad

Insecticidal (dihalopropenyl) phenylalkyl substituted dihydrobenzofuran and dihydrobenzopyran derivatives

Insecticidal (dihalopropenyl) phenylalkyl substituted dihydrobenzofuran and dihydrobenzopyran derivatives of Formula I are disclosed. These compounds provide unexpected insecticidal activity across a spectrum of insect pests combined with desirable physical properties including improved photostability. wherein x and y are integers independently selected from 0 or 1; and B is a bridging group *—(CR16R17)q—(CR18R19)r—(CR20R21)s—Lt—(CR22R23)u—(CR24R25)v—(CR26R27)w—, where the asterisk denotes attachment at A; and q, r, s, u, v and w are integers independently selected from 0, 1 and 2; and t is an integer selected from 0 and 1. A, D, E, G, M, R through R11, and R16 through R27, inclusively, are fully described herein. In addition, compositions comprising an insecticidally effective amount of at least one compound of formula I and methods of controlling insects by applying said compositions to a locus where insects are present or are expected to be present are also disclosed.

Dihalopropene compounds, their use as insecticides/acaricides and intermediates for their production

PCT No. PCT/JP97/00141 Sec. 371 Date Jun. 12, 1998 Sec. 102(e) Date Jun. 12, 1998 PCT Filed Jan. 1, 1997 PCT Pub. No. WO97/28112 PCT Pub. Date Aug. 7, 1997Dihalopropene compounds of the general formula: wherein R1 is substituted alkyl; R2, R3 and R4 are e

Dihalopropene compounds, insecticidal/acaricidal agents containing same, and intermediates for their production

The dihalopropene compounds of the general formula ?I! have excellent insecticidal/acaricidal activity, so that they are satisfactorily effective for the control of noxious insects, mites and ticks.