10411-85-5

Usage

InChI:InChI=1/C8H5Cl3O2/c1-13-7-5(10)3-2-4(9)6(7)8(11)12/h2-3H,1H3

Upstream product

• 1430103-09-5 2-(3-carboxyethyl-propyl)-6-dicambyl-3(2H)-pyridazinone 
• 101191-07-5 dicamba 2-nitrobenzyl ester 
• 1430103-01-7 3-cyano-4,6-di-t-butyl-2-pyridone dicamba ester 
• 1430102-99-0 2-(2-cyanoethyl)-6-dicambyl-3(2H)-pyridazinone 
• 1430102-98-9 2-(3-oxopropyl)-6-dicambyl-2,3-dihydro-3-pyridazinone 
• 1430102-97-8 2-(3-oxobutyl)-6-dicambyl-2,3-dihydro-3-pyridazinone 
• 1430102-83-2 dicamba 4-butoxyphenacylmethyl ester 
• 1430102-82-1 dicamba 4-methoxyphenacylmethyl ester 
• 1918-00-9 3,6-dichloro-O-anisic acid 

Downstream Products

• 16010-39-2 N,N-dimethyl-2-methoxy-3,6-dichlorobenzamide 
• 1430102-78-5 dicamba 6-nitroveratryl alcohol ester 
• 1430102-79-6 dicamba 2-nitrobenzyl ester 
• 1430102-80-9 dicamba 2-iodoethanol ester 
• 1430102-81-0 dicamba 2-(2-nitrobenzoxy)ethanol ester 
• 1918-00-9 3,6-dichloro-O-anisic acid 
• 1430102-86-5 dicamba 2-hydroxypyridine ester 
• 1430102-87-6 dicamba maleic hydrazide diester 
• 1430102-88-7 dicamba phthalhydrazide diester 
• 1430102-91-2 dicamba bromoxynil ester 
• 101191-21-3 dicamba 4-methoxybenzyl ester 
• 1430102-93-4 dicamba 4-methoxyphenol ester 
• 1430102-94-5 ethyl 2-(2-nitrobenzyl dicambyl)acrylate 
• 1430102-97-8 2-(3-oxobutyl)-6-dicambyl-2,3-dihydro-3-pyridazinone 

Relevant academic research and scientific papers

Pyrazole compound, salt and uses thereof,

The invention discloses a pyrazole compound and a salt thereof, wherein the structural formula of the pyrazole compound is represented by a formula (I). According to the invention, the pyrazole compound has good prevention and control effect on various gr

A including wo carboxylic acid ester compound and use thereof

The invention belongs to the field of agricultural herbicides, and concretely relates to an oxime-containing carboxylate compound and a use thereof. The oxime-containing carboxylate compound is represented by general formula (I), has very good weeding activity, can effectively control barnyard grass, piemarker, setaria viridis, Zinnia elegans and other weeds, realizes a very good weeding effect under a low dosage, is highly safe to crops, is especially safe to corn and rice (post-emergence), and can be used as a herbicide in the agricultural field.

LABILE ESTERS OF AGROCHEMICALS FOR CONTROLLED RELEASE AND REDUCTION OF OFF-SITE MOVEMENT

The present invention relates to esters of carboxylic acid agrochemicals comprising a labile protecting group and having formula (I). Certain of the esters of carboxylic acid agrochemicals do not undergo hydrolysis to a significant degree in the dark, but are cleaved to regenerate the parent carboxylic acid agrochemical when exposed to light. Others of the esters of carboxylic acid agrochemicals undergo hydrolysis under both light and dark conditions. The present invention further relates to methods for the controlled release of a carboxylic acid agrochemicals, and to methods of controlling unwanted plants comprising applying to the unwanted plants an ester of a carboxylic acid agrochemical.

Acyl derivatives of 2-aminobenzimidazole and their fungicide activity

Procedures have been developed for the preparation of methyl 2-benzimidazolylcarbamate, 2-acetylaminobenzimidazole, 2- benzoylaminobenzimidazole, 2-(3,5-dibromo-2-hydroxybenzoylamino)benzimidazole, 1-(3,6-dichloro-2-methoxybenzoyl)-2-aminobenzimidazole, 2-(3,5-dichloro-2- hydroxybenzoylamino)benzimidazole, 2-(3,5-dichloro-2-methoxybenzoylamino) benzimidazole, and 1-(3,5,6-trichloro-2-methoxybenzoyl)-2-aminobenzimidazole. The synthesized compounds have been tested for fungicide activity.

Hydrazides and hydroxamic acid derivatives

The present invention relates to hydrazides and hydroxamid acid derivatives of formula I and formula II wherein Y is Cl or OCH3;, A is O-alkylene of 1 to 5 carbon atoms, O-alkenylene of 3 to 6 atoms in which the unsaturation is non-adjacent to

3,6-dichloro-2-methoxybenzohydroxamic acid derivatives and use as herbicidal agents

Disclosed are herbicidal compounds of the general formula I: STR1 wherein A is O-alkylene of 1 to 5 carbon atoms, O-alkenylene of 3 to 6 carbon atoms in which the unsaturation is non-adjacent the oxygen atom thereof or NH-alkylene in which the alkylene is