6271-08-5

Usage

Uses

Used in Agricultural Industry:
2-CHLORO-N-(2,4-DINITRO-PHENYL)-ACETAMIDE is used as a herbicide for controlling the growth of unwanted plants. It is effective in managing various types of weeds that can compete with crops for nutrients and space, thereby ensuring healthier and more productive agricultural yields.
Used in Pest Control Industry:
In the pest control industry, 2-CHLORO-N-(2,4-DINITRO-PHENYL)-ACETAMIDE is used as an insecticide to manage insect pests. It targets the nervous systems of insects, leading to their paralysis and eventual death, thus protecting crops from damage caused by these pests.
It is crucial to handle 2-CHLORO-N-(2,4-DINITRO-PHENYL)-ACETAMIDE with care due to its potential toxicity to humans and animals if ingested or inhaled. Therefore, strict safety measures and regulatory guidelines should be adhered to during its application to minimize risks to both people and the environment.

InChI:InChI=1/C8H6ClN3O5/c9-4-8(13)10-6-2-1-5(11(14)15)3-7(6)12(16)17/h1-3H,4H2,(H,10,13)

Upstream product

• 79-04-9 chloroacetyl chloride 
• 97-02-9 2,4-Dinitroanilin 
• 541-88-8 Chloroacetic anhydride 

Downstream Products

• 97457-62-0 3-Hydroxy-benzo[b]thiophene-2-carboxylic acid (2,4-dinitro-phenyl)-amide 
• 14625-39-9 2-(chloromethyl)-6-nitro-1H-benzo[d]imidazole 
• 849435-69-4 N-(2-amino-4-nitro-phenyl)-2-chloro-acetamide 
• 63238-02-8 4-amino-2-methylsulfanyl-thiazole-5-carboxylic acid 2,4-dinitro-anilide 
• 63238-23-3 [3-(2,4-dinitro-phenyl)-4-oxo-thiazolidin-2-ylidene]-cyanamide 

Relevant academic research and scientific papers

Synthesis, X-Ray Crystallography, Theoretical Investigation and Optical Properties of 2-Chloro-N-(2,4-dinitrophenyl) Acetamide

Abstract: 2-Chloro-N-(2,4-dinitrophenyl) acetamide, 1, was synthesized and characterized by 1H and 13C NMR spectroscopy, ESI–MS, X-ray crystallography, and elemental analysis. This compound crystallizes in the monoclinic space group

Synthesis, Molecular Docking and Biological Evaluation of 2-Aryloxy-N-Phenylacetamide and N′-(2-Aryloxyoxyacetyl) Benzohydrazide Derivatives as Potential Antibacterial Agents

A new class of 2-aryloxy-N-phenylacetamide and N′-(2-aryloxyoxyacetyl) benzohydrazide derivatives with different active moieties were synthesized and screened for their antibacterial activity. Structural characterization of synthesized compounds was perfo

Synthesis and biological studies of N-phenyl substituted 2-(-5-(pyridine-4-yl)-1,3,4-oxadiazole-2-yl thio)acetamides

As oxadiazole have proven to be good antimicrobial agents, Antitubercular, analgesic (peripheral and central) and antiinflammatory agents. A new series of oxadiazole derivatives were synthesized and characterized by 1H NMR, IR, GCMS sophisticated analytical instruments and were evaluated for their antimicrobial activity, antitubercular activity, toxicity as per standard guidelines, analgesic (peripheral and central) and antiinflammatory activity. Out of several derivatives synthesized a few of N-phenyl substituted 2-(5-(pyridine-4- yl)-1,3,4-oxadiazole-2-yl thio)acetamide explores good antimicrobial activity by using Cup-Plate method, antitubercular activity by middle brook 7H9 agar medium against H37Rv, analgesic activity by Writhing and Tail immersion method and antiinflammatory by rat paw edema method.

Baker's yeast-mediated regioselective reduction of 2,4-dinitroacylanilines: Synthesis of 2-substituted 6-nitrobenzimidazoles

Several 2,4-dinitro-N-acylanilines were regioselectively reduced at the C-2 position by baker's yeast in slightly basic media (pH = 7.5) to afford 2-amino-4-nitroacylanilines, which were then cyclized under acidic conditions to the corresponding 2-substituted-6-nitrobenzimidazoles. The benzimidazoles thus obtained can be employed as precursors for bioactive derivatives.

Activities of 2-carboxanilido 3-hydroxybenzo[b]thiophens against molluscs Biomphalaria

The title compounds are shown to be nearly as active against molluscs as Niclosamide when they are either dihalogenated or monohalogenated and mononitrated on the benzene ring.