26650-76-0

Usage

Uses

Used in Polymer and Coating Industry:
2-(allyloxy)-4,6-dichloro-1,3,5-triazine is used as a crosslinking agent for improving the durability and strength of polymers and coatings. Its ability to form strong chemical bonds with other materials results in enhanced performance characteristics such as resistance to wear, corrosion, and environmental factors.
Used in Agricultural Industry:
In the agricultural sector, 2-(allyloxy)-4,6-dichloro-1,3,5-triazine is utilized as a herbicide to control and prevent the growth of unwanted weeds. Its effectiveness in managing weed populations contributes to maintaining the health and productivity of crops, thereby supporting sustainable farming practices.
It is crucial to manage the use and disposal of 2-(allyloxy)-4,6-dichloro-1,3,5-triazine with care due to its potential toxicity to aquatic life, ensuring that it does not contaminate water sources and harm the ecosystem.

InChI:InChI=1/C6H5Cl2N3O/c1-2-3-12-6-10-4(7)9-5(8)11-6/h2H,1,3H2

Upstream product

• 108-77-0 1,3,5-trichloro-2,4,6-triazine 
• 107-18-6 allyl alcohol 

Downstream Products

• 1267551-15-4 C₄₂H₃₀Cl₃N₉O₆ 

Relevant academic research and scientific papers

Synergistic effect of copolymeric resin grafted 1,2-benzisothiazol-3(2H)-one and heterocyclic groups as a marine antifouling coating

In order to find a new type of antifouling coating with higher biological activity and more environmental protection, heterocyclic compounds and benzisothiazolinone were introduced into acrylic resin to prepare a new type of antifouling resin. In this stu

Development of Triazinone-Based Condensing Reagents for Amide Formation

Novel triazinone-based condensing reagents have been developed. The palladium-catalyzed O-N allylic rearrangement of 2-(allyloxy)-4,6-dichloro-1,3,5-triazine and subsequent regioselective substitution using alcohols and an amine afforded chlorotriazinones, which can be readily converted using N-methylmorpholine into the corresponding condensing reagents. The condensation of carboxylic acids and amines using these reagents proceeded to afford the desired amides in good yields. In comparison with 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride, the newly synthesized triazinone-based condensing reagents exhibited higher reactivity.

Spectroscopic and fluorescence studies on Mn(II), Co(II), Ni(II) and Cu(II) complexes with NO donor fluorescence dyes

The reactions of the two common dyes [2TMPACT and 4PENI] with Mn(II), Co(II), Ni(II) and Cu(II) ions were done. All the isolated complexes have been characterized by physicochemical and spectroscopic techniques. The IR data reflect the bidentate mode of 2TMPACT towards the mononuclear complex [Mn(II)] even its tetradentate in binuclear complexes [Co(II) and Cu(II)]. However, the bidentate mode is the only behavior of 4PENI ligand towards each metal ion in its mononuclear complexes. The UV-vis spectral analysis beside the magnetic moment measurements are proposed different geometries concerning each metal ions with the two ligands under investigation, as the Mn(II)-2TMPACT complex is an octahedral but Mn(II)-4PENI is a tetrahedral geometry. All the synthesized compounds are thermogravimetrically investigated. The proposed thermal decomposition was discussed for each compound with each step as well as, the kinetic parameters were calculated for all preferrible decomposition steps. The mass spectroscopy tool was used to emphasis on the suitable molecular formula proposed and the fragmentation patterns were displayed. The fluorescence properties of the synthesized ligands and their complexes were studied in DMSO at room temperature.

Synthesis and functionalization of heteroatom-bridged bicyclocalixaromatics, large molecular triangular prisms with electron-rich and -deficient aromatic interiors

The synthesis and functionalization of oxygen and nitrogen atom bridged bicyclocalixaromatics of triangular prism structures are reported. By means of a fragment coupling approach, molecular triangular prisms of electron-rich and electron-deficient aromatic interiors were prepared using 1,3,5-tri(p- hydroxyphenyl)benzene and 2,4,6-tri(p-aminophenyl) triazine as base units and chlorotriazines as pillars. Aromatic nucleophilic substitution reaction of chlorotriazine moieties with functionalized amines led to triangular prisms with functionalizations on the peripheral edge positions, while functionalized triangular prisms on the vertex nitrogen positions were obtained using 2,4,6-tri[(p-allylamino)phenyl]-triazine derivative as a starting material. Symmetrical and distorted molecular triangular prisms in the solid state were revealed by X-ray crystallography. As evidenced by NMR spectroscopic data, however, all cage molecules synthesizedmost probably adopted highly symmetric triangular prism structures in solution phase. The functionalized shape-persistent triangular prism structures might find applications in molecular recognition and in the construction of higher and more sophisticated molecular architectures in supramolecular chemistry.