77989-15-2

Usage

Uses

Used in Organic Synthesis:
2-(2-bromophenyl)-4,6-diphenyl-1,3,5-triazine is used as a building block in organic synthesis for the creation of complex organic molecules. Its unique structure allows for versatile chemical reactions, facilitating the synthesis of a wide range of compounds with potential applications in various industries.
Used in Material Science:
In the field of material science, 2-(2-bromophenyl)-4,6-diphenyl-1,3,5-triazine is utilized as a component in the development of new materials. Its specific properties, such as its molecular structure and the presence of a bromine atom, can contribute to the creation of materials with tailored characteristics for specific applications.
Used in Pharmaceutical Research:
2-(2-bromophenyl)-4,6-diphenyl-1,3,5-triazine is used as a starting material in pharmaceutical research for the development of new drugs. Its unique chemical structure may offer novel pharmacological properties, which could be harnessed to address various medical conditions. Further research is necessary to determine its potential therapeutic applications and effects.
Used in Biological Studies:
In biological research, 2-(2-bromophenyl)-4,6-diphenyl-1,3,5-triazine may be employed as a tool to study biological processes and interactions. Its unique structure could provide insights into molecular recognition, binding, and other biological phenomena, contributing to a better understanding of biological systems and potentially leading to the discovery of new therapeutic agents.

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Relevant academic research and scientific papers

Nitrogen-containing compound, electronic element, and electronic device

The invention belongs to the technical field of organic materials, and provides a nitrogen-containing compound, an electronic element and an electronic device. The structure of the nitrogen-containingcompound is shown as a formula 1, wherein X1, X2 and X3 are respectively and independently selected from C or N, and at least one of X1, X2 and X3 is N; wherein R1, R2 and R3 are respectively and independently selected from hydrogen or a group shown in a chemical formula 1-1, and only one of R1, R2 and R3 is a group shown in a chemical formula 1-1. The nitrogen-containing compound can improve theperformance of an electronic component.

Synthesis, Spectra, and Theoretical Investigations of 1,3,5-Triazines Compounds as Ultraviolet Rays Absorber Based on Time-Dependent Density Functional Calculations and three-Dimensional Quantitative Structure-Property Relationship

A series of 1,3,5-triazines were synthesized and their UV absorption properties were tested. The computational chemistry methods were used to construct quantitative structure-property relationship (QSPR), which was used to computer aided design of new 1,3,5-triazines ultraviolet rays absorber compounds. The experimental UV absorption data are in good agreement with those predicted data using the Time-dependent density functional theory (TD-DFT) [B3LYP/6–311 + G(d,p)]. A suitable forecasting model (R > 0.8, P 0.0001) was revealed. Predictive three-dimensional quantitative structure-property relationship (3D-QSPR) model was established using multifit molecular alignment rule of Sybyl program, which conclusion is consistent with the TD-DFT calculation. The exceptional photostability mechanism of such ultraviolet rays absorber compounds was studied and confirmed as principally banked upon their ability to undergo excited-state deactivation via an ultrafast excited-state proton transfer (ESIPT). The intramolecular hydrogen bond (IMHB) of 1,3,5-triazines compounds is the basis for the excited state proton transfer, which was explored by IR spectroscopy, UV spectra, structural and energetic aspects of different conformers and frontier molecular orbitals analysis.

Sulfur Nitride in Organic Chemistry. 9. The Reaction of Tetrasulfur Tetranitride with Benzyl Ketones. Preparation of 3,4-Disubstituted-1,2,5-thiadiazoles

The reaction of tetrasulfur tetranitride (1) with various aryl and benzyl ketones (2a-o), oxindole (11), benzyl α-pyridyl ketone (12) and α-phenacylpyridine (13) afforded the corresponding 1,2,5-thiadiazoles (3a-n, 11 and 14).The scope and limitations of the above reaction were investigated and the evidences suggesting the radical anion mechanism are presented.