94051-08-8

Usage

InChI:InChI=1/C17H13ClN2O4/c1-10(17(21)22)23-12-3-5-13(6-4-12)24-16-9-19-15-8-11(18)2-7-14(15)20-16/h2-10H,1H3,(H,21,22)/t10-/m1/s1

Upstream product

• 76578-14-8 (R)-2-[4-[(6-chloro-2-quinoxalinyl)oxy]phenoxy]propanoic acid ethyl ester 
• 57057-80-4 ethyl (S)-2-[[(4-methylphenyl)sulfonyl]oxy]propanoate 
• 76578-79-5 6-chloro-2-(4-hydroxyphenoxy)quinoxaline 
• 18671-97-1 2,6-dichloroquinoxaline 
• 94050-90-5 (R)-2-(4-hydroxyphenoxy)propionic acid 

Relevant academic research and scientific papers

Development of an enzyme-linked immunosorbent assay for quantitative determination of quizalofop-p-ethyl

Accurate quantification of quizalofop-p-ethyl is essential for it may do harm to humans and animals through both water and food. Currently, detection of quizalofop-p-ethyl mainly relies on methods such as gas chromatography, high performance liquid chroma

Design, Synthesis and Biological Activity of 2-(4-Aryloxyphenoxy) Propionamides Containing 1,3,4-Thiadiazole

Four new 2-(4-aryloxyphenoxy) propionamides containing 1,3,4-thiadiazole moiety were synthesized based on the structure of Quizalofop-P. The structures of the synthesized compounds were confirmed by 1H nuclear magnetic resonance, elemental analysis, and optical rotation. The herbicidal bioassay showed that the title compounds had good herbicidal activity against barnyard grass.

Synthesis and herbicidal activity of 2-(4-aryloxyphenoxy)propionamides

Two novel 2-(4-aryloxyphenoxy)propionamide derivatives were synthesized based on the structure of metamifop. Their structures were confirmed by 1H nuclear magnetic resonance, elemental analysis, and optical rotation. The preliminary bioassay re

Tetrahydroisoquinoline-2-aryloxyphenoxyalkyl ketone compound and application thereof

The invention discloses a tetrahydroisoquinoline-2-aryloxyphenoxyalkyl ketone compound and application thereof. The chemical structural formula of the compound is shown in formula I or II shown in the description, where each of R, R, R and R i

Pyridyl-3-yl-aryloxyphenoxynoic acid ester compounds and application thereof

The invention discloses pyridyl-3-yl-aryloxyphenoxynoic acid ester compounds and herbicidal activities thereof. The chemical structural formula is disclosed as Formula I or II, wherein X is nitrogen or carbon; Y is -N=CH- or oxygen; X1, X2 and X3 are resp

2-(4-aryloxy phenoxy)montanic acid naphthalene ester compound and application thereof

The invention discloses a 2-(4-aryloxy phenoxy)montanic acid naphthalene ester compound and application thereof as a herbicide. The chemical structural formula of the 2-(4-aryloxy phenoxy)montanic acid naphthalene ester compound is shown as the formula I

Condensed heterogeneous oxyphenoxy carboxylic acid derivative and application thereof

The invention discloses a condensed heterogeneous oxyphenoxy carboxylic acid derivative and weeding activity thereof. The chemical structural formula of the condensed heterogeneous oxyphenoxy carboxylic acid derivative is as shown by a formula I as shown

Aryloxyphenoxy alkane acid derivative with biological activity and preparation method thereof

The invention discloses an aryloxyphenoxy alkane acid derivative and herbicidal activity thereof. The chemical structural formula of the derivative is shown as a formula I or II, and the structural formula is as shown in the specification, wherein R1 is a

N - (aryl alkoxy) fragrant oxygen benzene oxygen carboxylic acid amide compound and its preparation method and application

The invention discloses N-(arylalkyloxy)aryloxy phenoxy carboxylic acid amide compounds show as a formula (I), and a preparation method and application thereof. In the formula (I), Ar1, Ar2, R1, R2, R3 and n are defined in the specification. The formula (

Preparing method of quizalofop-p-ethyl preparation

The invention belongs to the field of pesticides, and provides a preparing method of a quizalofop-p-ethyl preparation. The preparing method of the quizalofop-p-ethyl preparation is characterized in that common preparing of the quizalofop-p-ethyl preparation is replaced, and a one-step method is adopted, namely, quizalofop-p-ethyl raw powder cannot be synthesized and produced, and the quizalofop-p-ethyl preparation can be directly produced and prepared. The preparing method of the quizalofop-p-ethyl preparation, provided by the invention, has the maximum advantages that resource integration is realized, crystallizing and drying steps are removed, the labor amount is reduced, the yield is increased, the production cost is reduced, and mother liquor-black oil is prevented from being generated. The preparing method can be used for preparing the following preparations: 5 to 25 percent of quizalofop-p-ethyl EC (Emulsifiable Concentrate), 5 to 15 percent of quizalofop-p-ethyl microemulsion, 5 to 10 percent of quizalofop-p-ethyl EW (Emulsion in Water), 5 to 50 percent of quizalofop-p-ethyl dry suspension concentrate, 5 to 20 percent of quizalofop-p-ethyl water suspension concentrate, quizalofop-p-ethyl oil suspension concentrate, quizalofop-p-ethyl composite EC, composite microemulsion, composite EW, composite dry suspension concentrate, composite water suspension concentrate and composite oil suspension concentrate.