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Usage

Uses

Used in Agricultural Applications:
2,4-dichloro-6-(propan-2-yl)-1,3,5-triazine is used as a herbicide for controlling weeds in agricultural fields. It is applied to prevent the growth of unwanted plants that can compete with crops for nutrients, sunlight, and space, thereby enhancing crop yield and quality.
Used in Horticultural Applications:
In horticulture, 2,4-dichloro-6-(propan-2-yl)-1,3,5-triazine is utilized as a weed control agent in gardens, lawns, and other cultivated landscapes. It helps maintain aesthetic appeal and promotes the healthy growth of desired plants by eliminating competing weeds.
Used in Forestry Applications:
2,4-dichloro-6-(propan-2-yl)-1,3,5-triazine is employed in forestry as a means to control weed growth that can hinder the development of trees and other valuable flora. Its use contributes to the sustainable management of forest ecosystems.
Used in Industrial Weed Control:
2,4-dichloro-6-(propan-2-yl)-1,3,5-triazine is also used in industrial areas to manage weed growth around infrastructure, storage facilities, and other industrial sites. It helps to keep these areas clear of vegetation that could pose safety hazards or reduce the efficiency of operations.
Used as a Pre-emergent Herbicide:
2,4-dichloro-6-(propan-2-yl)-1,3,5-triazine is applied as a pre-emergent herbicide to prevent the growth of weeds before they emerge from the soil. This application type is particularly useful for maintaining weed-free areas over extended periods without the need for repeated treatments once the weeds have been initially controlled.

Upstream product

• 108-77-0 1,3,5-trichloro-2,4,6-triazine 
• 1068-55-9 isopropylmagnesium chloride 

Relevant academic research and scientific papers

Combinatorial solid-phase synthesis of 4,6-diaryl and 4-aryl, 6-alkyl-1,3,5-triazines and their application to efficient biofuel production

Herein we report the solid-phase synthesis of a combinatorial aryl, alkyl-triazine library and its application to biofuel production. The combination of Grignard reactions and solid supported Suzuki coupling reactions afforded unique 120 triazine compounds with high purities and minimum purification steps. Through an unbiased phenotypic screening for improved biofuel generation in oleaginous yeast, we found one diaryl triazine derivative (E4) which increased the biolipid production up to 86%.

Novel orthogonal synthesis of a tagged combinatorial triazine library via grignard reaction

To expand the diversity of 1,3,5-triazine libraries to aryl and alkyl functionalities through the CC bond, we employed a novel orthogonal synthesis via Grignard monoalkylation or monoarylation of cyanuric chloride in solution to prepare aryl- or alkyl-substituted triazine building blocks. These aryl- or alkyl-substituted triazine building blocks were captured by a resin-bound amine, followed by amination and acidic cleavage with high purity. Herein, we demonstrate a novel orthogonal synthesis of a tagged aryl- and alkyl-triazine library on solid support, utilizing building blocks prepared via Grignard reaction in solution. Through incorporation of a triethylene glycol linker at one of the alternate sites on the triazine scaffold we explored an intrinsic tagged library approach. CSIRO 2009.

Anarchy in the solid state: structural dependence on glass-forming ability in triazine-based molecular glasses

We have recently shown that molecular glasses, small molecules capable of readily forming glassy solids as opposed to crystals, can be designed by exploiting molecular association through strong and directional intermolecular interactions, as exemplified by several members of the bis(mexylamino)triazine family. Herein, 43 new bis(mexylamino)triazine derivatives were synthesized, 31 of which have been found to spontaneously form glassy phases and did not crystallize upon heating. Crown Copyright

Synthesis and biological evaluation of novel 1,3,5-triazine derivatives as antimicrobial agents

Numerous studies have contributed to the development of natural and synthetic antimicrobial peptides as a prospective source of antibiotic agents. Based on the concept that cationic charge, bulk, and lipophilicity are major factors determining antibacterial activity in these peptides, we designed and screened several combinatorial libraries based on 1,3,5-triazine as a template. A set of compounds were identified to show potent antimicrobial activity together with low hemolytic activity.

S-TRIAZINE COMPOUNDS, PHARMACEUTICAL COMPOSITIONS AND METHODS OF USING THE SAME

Novel s-triazine compounds are disclosed and represented by the following: formula (Ia). The compounds may be prepared as pharmaceutical compositions, and may be used for the prevention and treatment of a variety of conditions in mammals including humans, where microbial infection is either a direct cause or a related condition.

2-Alkyl-4,6-dialkylamino-1,3,5-triazines via Grignard alkylation of cyanuric chloride: An aged reaction revisited

Suitable one-pot reaction conditions are suggested to prepare, in good overall yields, some 2-(alk-1'-ynyl)- and 2-alkyl-4,6-dialkylamino-1,3,5-triazines via reaction of cyanuric chloride with Grignard reagents followed by amination. (C) 2000 Elsevier Science Ltd.