4682-78-4Relevant articles and documents
1,3,5-Triazine as core for the preparation of dendrons
Albericio, Fernando,El-Faham, Ayman,Kumar, Ashish,Sharma, Anamika,Sheyi, Rotimi,de la Torre, Beatriz G.
, (2020)
A unique property of 2,4,6-trichloro-1,3,5-triazine (TCT) is its ability to undergoes a nucleophilic aromatic substitution reaction (SNAr) under temperature-controlled conditions. Using a convenient and biologically friendly protocol, mono-substituted s-t
Novel Triazine Derivatives and Thermo-curable or Photosensitive Composition Comprising the Same
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Paragraph 0299-0303, (2021/03/30)
A compound represented by any one of Formulas A to [Chemical Formula C] and a photosensitive composition or a thermosetting composition including the same are disclosed. [Chemical Formula A] to [Chemical Formula C] The structure of a compound represented
Triazine natural gas drag reducer as well as synthesis method and application thereof
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Paragraph 0020; 0029-0032; 0046-0049, (2020/04/29)
The invention discloses a triazine natural gas drag reducer. The molecular structural formula of the drag reducer is shown in the description. A synthesis method of the drag reducer comprises the following steps: dissolving cyanuric chloride in a solvent, dropwise adding an alcohol and an inorganic alkali at -15-0 DEG C, carrying out a reaction at -15-0 DEG C for 2-6 h, adding morpholine and the inorganic alkali after the reaction ends, carrying out a reaction at 50-100 DEG C for 6-12 h, washing the obtained reaction product with water after the reaction ends, and drying the washed reaction product to obtain the product. The drag reducer has a multi-polar end and a non-polar end, and has a good adsorption performance and excellent drag reducing and transportation increasing effects. The synthesis method has the advantages of simplicity, mild conditions, short time, low device requirements, and easiness in realization of large-scale industrial production.