26650-75-9

Usage

Uses

Used in Agricultural Industry:
2,4-DICHLORO-6-N-PROPOXY-1,3,5-TRIAZINE is used as a herbicide for controlling the growth of broadleaf weeds and some grasses in various crops. It is applied to selectively target unwanted plants, ensuring the desired crops remain relatively unharmed. This selective action is crucial for maintaining crop health and productivity while minimizing the impact on non-target plants.
It is important to handle 2,4-DICHLORO-6-N-PROPOXY-1,3,5-TRIAZINE with caution due to its potential harmful effects if ingested or inhaled, and its potential to cause skin and eye irritation. Proper safety measures should be taken during its application to minimize exposure and ensure the safety of both the environment and the individuals involved in its use.

InChI:InChI=1/C6H7Cl2N3O/c1-2-3-12-6-10-4(7)9-5(8)11-6/h2-3H2,1H3

Upstream product

• 71-23-8 propan-1-ol 
• 108-77-0 1,3,5-trichloro-2,4,6-triazine 

Relevant academic research and scientific papers

Oxygen catalyzed mobilization of iron from ferritin by iron(iii) chelate ligands

Tridentate chelate ligands of 2,6-bis[hydroxy(methyl)amino]-1,3,5-triazine family rapidly release iron from human recombinant ferritin in the presence of oxygen. The reaction is inhibited by superoxide dismutase, catalase, mannitol and urea. Suggested rea

IMPROVEMENT OF THE SELECTIVITY OF ALKOXYLATION OF CYANURIC CHLORIDE.

Study of the quantitative relationships of the alkoxylation reaction and optimization of the complex reaction based on a mathematical model show that individual monoalkoxy-s-triazines free from 5-15% of dialkoxy-s-triazines cannot be obtained in aqueous acetone solutions. It is found that if the reaction is conducted in the basic bipolar aprotic solvent dimethylacetamide it proceeds selectively with exclusive formation of monoalkoxy-s-triazines. It can be seen from the data that the nature of the solvent does not affect selectivity of the reaction significantly. It is shown that when cyanuric chloride reacts with amides left bracket dimethylformamide (DMFA), N-methylformamide right bracket hygroscopic hydrolytically unstable products of the salt type are formed. The intermediates react with nucleophiles, such as aniline, to form substituted triazines. The reaction proceeds analogously with alcohols, and the hydrogen chloride evolved is bound irreversibly by dimethylacetamide.