136197-77-8

Usage

Uses

Used in Agricultural Industry:
2,4-Imidazolidinedione, 3-[(4-chlorophenyl)methyl]is utilized as a pesticide and herbicide for the purpose of inhibiting the growth of weeds and pests. Its effectiveness in crop protection is attributed to its ability to control unwanted plant and insect species that could otherwise damage or reduce crop yields. However, due to its potential harmful effects if ingested or inhaled, it is imperative that this chemical is handled with care and in strict adherence to safety guidelines.

Upstream product

• 461-72-3 2,4-imidazolidinedione 
• 622-95-7 4-chlorobenzyl bromide 
• 98634-73-2 potassium 2,5-dioxoimidazolidin-1-ide 
• 104-83-6 1-Chloro-4-(chloromethyl)benzene 

Downstream Products

• 141647-74-7 3-(4-chlorobenzyl)-5-(3-methylbenzylidene)-2,4-imidazolidinedione 
• 170462-10-9 3-(4-Chlorobenzyl)-4-thioxoimidazolidine-2-one 
• 137608-84-5 3-(4-chlorobenzyl)-5-(2-fluorobenzylidene)-2,4-imidazolidinedione 
• 141647-75-8 3-(4-chlorobenzyl)-5-(4-methoxybenzylidene)-2,4-imidazolidinedione 
• 137608-82-3 3-(4-chlorobenzyl)-5-(4-nitrobenzylidene)-2,4-imidazolidinedione 
• 141647-73-6 3-(4-chlorobenzyl)-5-(4-methylbenzylidene)-2,4-imidazolidinedione 

Relevant academic research and scientific papers

Synthesis and antidiabetic activity of some new chromonyl-2,4- thiazolidinediones

A series of chromonyl-2,4-thiazolidinediones (VIa-f) and chromonyl-2,4-imidazolidinediones (VIIa-f) was prepared by Knoevenagel reaction of substituted benzyl-2,4-thiazolidinediones (IVa-f) and substituted benzyl-2,4-imidazolidinediones (Va-f) with chromo

Aralkyl and aralkylidene heterocyclic lactams and imides

The present invention relates to compounds of the formula I wherein R1, R2, R3, X, Y and the dashed line are as defined in the specification, to intermediates for their preparation, to pharmaceutical compositions containin

Aralkyl and aralkylidene heterocyclic lactams and imides

The present invention relates to compounds of the formula I wherein R1, R2, R3, X, Y and the dashed line are as defined in the specification, to intermediates for their preparation, to pharmaceutical compositions containin

Synthesis and structural study of 5-arylidene thiazolidine-2,4-diones and 3-substituted-4-thio-imidazolidine-2-ones

The synthesis and the physico-chemical properties of four 3-(4-bromophenacyl)-5-arylidene-thiazolidine-2,4-diones, two 3-(4-bromobenzyl)-5-arylidene-thiazolidine-2,4-diones and seven 3-(4-chlorobenzyl)-5-arylidene-4-thio-imidazolidine-2-ones were described. These products were synthetized by the aldolisation-crotonisation reaction between aromatic aldehydes and substituted thiazolidinediones or thio-imidazolidinones.

Synthesis and antimicrobial activity of chlorobenzyl benzylidene imidazolidinediones and substituted thiazolidinediones

The synthesis of five chlorobenzyl benzylidene imidazolidinediones and four fluorobenzyl benzylidene thiazolidinediones is described. In order to investigate their antimicrobial activity they are evaluated against microorganism such as Candida albicans, Neurospora crassa, Staphylococcus aureus, Myocobacterium smegmatis and Escherichia coli.