22065-34-5

Usage

Uses

Used in Chemical Synthesis:
Benzenamine, 4,4',4''-[1,3,5-triazine-2,4,6-triyltris(oxy)]trisis utilized as a versatile building block in chemical synthesis for its ability to create strong and stable bonds with other molecules, contributing to the production of a variety of industrial products.
Used in Dye Production:
In the dye industry, Benzenamine, 4,4',4''-[1,3,5-triazine-2,4,6-triyltris(oxy)]trisis used as a key component in the formulation of dyes, leveraging its chemical properties to enhance colorfastness and stability.
Used in Pharmaceutical Development:
Benzenamine, 4,4',4''-[1,3,5-triazine-2,4,6-triyltris(oxy)]trisis employed as a precursor in the development of new pharmaceuticals due to its potential bioactive properties, offering a foundation for the creation of innovative drugs.
Used in Agricultural Chemicals:
In the agricultural sector, Benzenamine, 4,4',4''-[1,3,5-triazine-2,4,6-triyltris(oxy)]tris- is used in the development of new agrochemicals, where its potential bioactivity is harnessed to improve crop protection and yield enhancement.
Each application underscores the importance of the compound's unique structural attributes and its role in advancing various industries through its integration into their product development pipelines.

Upstream product

• 1919-18-2 2,4,6-tris(4-nitrophenoxy)-1,3,5-triazine 

Relevant academic research and scientific papers

Self-assembly and steric hindrance for further host–guest interactions of a tetrahedral cage FeII4L4

In this paper, a novel complex [FeII4L4]8+ was designed and synthesized from subcomponent self-assembly of C3-symmetric 2,4,6-tris(4-aminophenoxy)triazine, 3-methylpyridine-2-carboxaldehyde and iron(II) trifluoromethanesulfonate in CH3CN solution. The structure of target compound was confirmed by 1H NMR and ESI-MS measurements as a tetrahedral cage, and the host–guest interactions between the complex and a series of guest molecules were studied. The results show that the intermolecular interactions are relatively weak by comparison with other similar ligand’s complexes, which may be due to the steric effect of methyl groups adjacent to the peripheral apertures of the cage.

Imine zinc s-triazine complex

The invention discloses an imine zinc s-triazine complex (I). The chemical formula of the imine zinc s-triazine complex (I) is shown in the description. The invention relates to the imine zinc s-triazine complex and a preparation method thereof. The imine zinc s-triazine complex is synthesized by self-assembly of p-triaminophenoxy s-triazine, zinc trifluoromethanesulfonate and 6-methylpyridine-2-formaldehyde under the effect of a sodium hexafluorophosphate ionic template.

Covalent organic frameworks: Efficient, metal-free, heterogeneous organocatalysts for chemical fixation of CO2 under mild conditions

The cycloaddition of CO2 to epoxides to form cyclic carbonates is very promising and does not generate any side products. Metal-free, heterogeneous organocatalysts offer an environmentally friendly alternative to traditional metal-based catalysts. Herein two triazine-based covalent organic frameworks (COF-JLU6 and COF-JLU7) were successfully synthesized under solvothermal conditions. The structural and chemical properties of COFs were fully characterized by using powder X-ray diffraction analysis, structural simulation, Fourier transform infrared spectroscopy, 13C solid-state NMR spectroscopy, electron microscopy, thermogravimetric analysis and nitrogen adsorption. The two COF materials combine mesopores, high crystallinity and good stability, as well as a large number of hydroxy groups in the pore walls. They possess a high Brunauer-Emmett-Teller (BET) specific surface area up to 1390 m2 g-1 and a large pore volume of 1.78 cm3 g-1. The COF-JLU7 displays a high CO2 uptake of 151 mg g-1 at 273 K and 1 bar. Importantly, COF-JLU7 was found to be a highly effective catalyst to convert CO2 into cyclic carbonate through the cycloaddition reaction with epoxides under mild conditions. The effect of reaction parameters, such as reaction temperature, reaction time and CO2 pressure, on the catalytic performance was also investigated in detail. Moreover, the new framework-based catalyst can be recovered and reused five times without a significant loss of catalytic efficiency.

A study on the co-reaction of benzoxazine and triazine through a triazine-containing benzoxazine

To study the co-reaction of benzoxazine and triazine, a triazine-containing benzoxazine (P-tta) was prepared through nucleophilic substitution of 4-(2H-benzo[e][1,3]oxazin-3(4H)-yl)phenol (P-ap) with 2,4,6-trichloro-1,3,5-triazine. DSC thermograms show th

A face-capped [Fe4L4]8+ spin crossover tetrahedral cage

Reported here is a face-capped Fe(ii) molecular tetrahedron, [Fe 4L4](BF4)8, 1. Single crystal X-ray diffraction at 153 and 293 K suggest spin crossover (SCO) and variable temperature magnetic susceptibility measurements confirm 1 displays thermally driven SCO behaviour in the solid state and in dilute acetone solution centred around 284-288 K. The Royal Society of Chemistry 2013.