32428-71-0

Usage

Uses

Used in Agricultural Industry:
2-Ethyl-6-methyl-2-chloroacetanilide is used as a herbicide for controlling grasses and broad-leaved weeds. It functions by inhibiting cell division in the targeted plants, which are absorbed through their roots, leading to the disruption of their growth.
Used in Pharmaceutical Industry:
2-Ethyl-6-methyl-2-chloroacetanilide is used as a precursor in the synthesis of pharmaceuticals. It acts as a stabilizer or intermediate in chemical reactions, contributing to the development of various medicinal compounds.
Used in Agrochemical Industry:
In the agrochemical industry, 2-Ethyl-6-methyl-2-chloroacetanilide is utilized in the production of other agrochemicals, leveraging its properties to enhance the effectiveness of these products in controlling unwanted plant growth.
It is crucial to handle 2-Ethyl-6-methyl-2-chloroacetanilide with care due to its potential harmful effects if it comes into contact with the skin or is ingested, emphasizing the need for proper safety measures during its use in various applications.

InChI:InChI=1/C11H14ClNO/c1-3-9-6-4-5-8(2)11(9)13-10(14)7-12/h4-6H,3,7H2,1-2H3,(H,13,14)

Upstream product

• 24549-06-2 6-ethyl-o-toluidine 
• 79-04-9 chloroacetyl chloride 

Downstream Products

• 133035-54-8 N-(2-Ethyl-6-methyl-phenyl)-2-(6-methoxy-2,2-dimethyl-4-oxo-chroman-7-yloxy)-acetamide 
• 133035-33-3 2-(2,2-Dimethyl-4-oxo-chroman-7-yloxy)-N-(2-ethyl-6-methyl-phenyl)-acetamide 
• 133035-37-7 N-(2-Ethyl-6-methyl-phenyl)-2-(2,2,5-trimethyl-4-oxo-chroman-7-yloxy)-acetamide 
• 133035-43-5 N-(2-Ethyl-6-methyl-phenyl)-2-(2,2,8-trimethyl-4-oxo-chroman-7-yloxy)-acetamide 
• 85232-12-8 2-Chloro-N-(2-ethoxy-ethoxymethyl)-N-(2-ethyl-6-methyl-phenyl)-acetamide 
• 85232-10-6 2-Chloro-N-(2-ethyl-6-methyl-phenyl)-N-(2-methoxy-ethoxymethyl)-acetamide 
• 76213-34-8 2-amino-2'-ethyl-6'-methylacetanilide 
• 84243-44-7 1-[(2-ethyl-6-methylphenyl)carbamoylmethyl]-2-methyl-2-imidazoline 
• 133035-87-7 N-(2-Ethyl-6-methyl-phenyl)-2-(4-hydroxy-6-methoxy-2,2-dimethyl-chroman-7-yloxy)-acetamide 
• 133035-82-2 N-(2-Ethyl-6-methyl-phenyl)-2-(4-hydroxy-7-methoxy-2,2-dimethyl-chroman-6-yloxy)-acetamide 
• 133035-76-4 N-(2-Ethyl-6-methyl-phenyl)-2-(4-hydroxy-2,2,8-trimethyl-chroman-7-yloxy)-acetamide 
• 133035-70-8 N-(2-Ethyl-6-methyl-phenyl)-2-(4-hydroxy-2,2,5-trimethyl-chroman-7-yloxy)-acetamide 
• 133035-64-0 N-(2-Ethyl-6-methyl-phenyl)-2-(4-hydroxy-2,2-dimethyl-chroman-7-yloxy)-acetamide 
• 133036-08-5 N-(2-Ethyl-6-methyl-phenyl)-2-(7-methoxy-2,2-dimethyl-2H-chromen-6-yloxy)-acetamide 

Relevant academic research and scientific papers

Design, synthesis, antibacterial and quorum quenching studies of 1,2,5-trisubstituted 1,2,4-triazoles

Abstract: In view of discovering novel bioactive molecules, 1-phenyl-1H-2-(1-aryl-5-methyl-1H-1,2,3-triazol-4-yl)-3-(N-aryl-carbamoylmethylthio)-1,2,4-triazoles (8a–n) were designed and synthesized in good yield. Preliminary antibacterial activity was tested against Chromobacterium violaceum and Xanthomonas campestris pv. Campestris (Xcc). Out of 14 derivatives, compound 8g selectively possessed antibacterial activity against C. violaceum. Further derivatives that possessed an electron-withdrawing group and halogen atoms in N-phenylacetamide moiety were moderately active against Xcc (plant pathogen). After observing the reduction of violacein production through plate assay, compounds 8a, 8c, 8h, 8i and 8m were subjected to quantification of quorum sensing inhibition. Compounds with the electron-withdrawing group in N-phenylacetamide moiety showed admirable activity with > 80% inhibition of violacein. Mainly compound 8c which was inactive against the growth of bacteria were identified as excellent QSI which could be a lead compound for further development. Graphic abstract: One of the best approaches to acquire anti-virulence strategies and new direction for the discovery of antibacterial drugs[Figure not available: see fulltext.]

MOLECULES HAVING CERTAIN PESTICIDAL UTILITIES, AND INTERMEDIATES, COMPOSITIONS, AND PROCESSES RELATED THERETO

This disclosure relates to the field of molecules having pesticidal utility against pests in Phyla Nematoda, Arthropoda, and/or Mollusca, processes to produce such molecules and intermediates used in such processes, compositions containing such molecules,