111544-93-5

Usage

Uses

Used in Agricultural Industry:
DIETHYL 2,4-DICHLOROPHENYL MALONATE is used as a precursor in the synthesis of pyrethroid insecticides for the agricultural industry. It is employed for its ability to effectively control pests by disrupting their nervous systems, thereby protecting crops from damage and ensuring a stable food supply.
As a key component in the production of pyrethroid insecticides, DIETHYL 2,4-DICHLOROPHENYL MALONATE contributes to the development of more potent and selective insect control solutions. Its use in this industry is crucial for maintaining crop yields and minimizing the impact of pests on agricultural productivity.
However, it is important to handle DIETHYL 2,4-DICHLOROPHENYL MALONATE with care, as it can also be harmful to humans and other non-target organisms. Proper safety measures and regulations must be followed to minimize potential risks and ensure the responsible use of this chemical compound in the agricultural sector.

InChI:InChI=1/C13H14Cl2O4/c1-3-18-12(16)11(13(17)19-4-2)9-6-5-8(14)7-10(9)15/h5-7,11H,3-4H2,1-2H3

Upstream product

• 41022-54-2 ethyl 2-(2, 4-dichlorophenyl)acetate 
• 105-58-8 Diethyl carbonate 
• 1193-72-2 1-bromo-2,4-dichlorobenzene 
• 105-53-3 diethyl malonate 

Relevant academic research and scientific papers

Synthesis of Conformationally Locked and C-Linked Analogues of Imidazole-Based Ketene Dithioacetal Fungicides

First examples with the unknown tricyclic 4,8 b -dihydro-3 aH -indeno[1,2- d ][1,3]dithiole ring system have been prepared. Also, imidazoles linked in ring position 5 to a ketene dithioacetal and 1,3-dithiane derivatives with an exocyclic cyano- and imidazole-substituted C-C double bond are completely new. All these compounds are either conformationally locked, C-linked or six-ring analogues of the antifungal agent luliconazole. Synthesis and fungicidal activity of these sterol biosynthesis inhibitors are reported.

Method for the production of substituted 2-aryl malonic acid esters

The present invention relates to a process for preparing substituted 2-arylmalonic esters of the general formula I in which R is C1-C6-alkyl or C1-C4-alkoxy-C1-C4-alkyl; Ar is phenyl or a heteroaromatic 5- or 6-membered ring; where each carbon atom present in the radicals mentioned above optionally carries a substituent RA; RA is F, Cl, CN, NO2, C1-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy, C1-C4-haloalkoxy, etc., or two adjacent substituents RA together with the carbon atoms to which they are attached form a ring; and where a malonic ester is reacted with a base and an aryl bromide in the presence of a copper salt, which comprises employing from 0.1 to 0.65 molar equivalents of the base per molar equivalent of the malonic ester.

Pyrimidine Non-Classical Cannabinoid Compounds and Related Methods of Use

Disclosed are compounds of the formula I: wherein R1, R2, V, W, X, Y and Z can be as defined herein. The compounds can be used in the treatment of disorders mediated by the cannabinoid receptors.

Pyridine Non-Classical Cannabinoid Compounds and Related Methods of Use

wherein R1, R2, V, W, X, Y and Z can be as defined herein. The compounds can be used in the treatment of disorders mediated by the cannabinoid receptors.