7753-13-1

Upstream product

• 767-00-0 4-cyanophenol 

Downstream Products

• 1063743-05-4 C₁₁₄H₁₇₇N₃O₉ 
• 1063742-97-1 C₇₈H₁₀₅N₃O₉ 
• 1063743-01-0 C₉₆H₁₄₁N₃O₁₂ 
• 1063743-09-8 C₁₅₀H₂₄₉N₃O₁₂ 
• 1395348-29-4 C₃₀H₂₁N₃O₃ 
• 1267551-02-9 2,4,6-tri(4-(4-butyloxy-6-chloro-1,3,5-triazin-2-yl)phenyl)-1,3,5-triazine 
• 1221509-86-9 C₃₉H₂₄Br₃N₃O₃ 
• 1135459-40-3 2,4,6-tris-(4-n-hexyloxyphenyl)-[1,3,5]triazine 

Relevant academic research and scientific papers

C3-Symmetric Positional Isomers of BODIPY Substituted Triazines: Synthesis and Excited State Properties

A series of meso-O-aryl functionalized BODIPY trimers positioned along the C3-symmetric axis of triazine ring have newly been synthesized to probe the ground and excited state intramolecular type interactions between the BODIPY entities within the trimer. The developed synthetic strategy resulted in BODIPY trimers in good yields. The electron rich, meso-O-aryl functionalized BODIPYs revealed larger HOMO-LUMO gap and higher Stokes shift and fluorescence lifetimes compared to the traditional BODIPY derivatives having an aryl group attached at the meso position. The optical absorption, steady-state fluorescence, and electrochemical studies revealed weak, if any, intramolecular type interactions among the BODIPY entities within the trimer and the central triazine unit to be both photo- and redox-salient. The possibility of singlet-singlet energy migration among the BODIPY entities was investigated using time-resolved emission and femtosecond transient absorption studies. Excitation of a BODIPY entity in the trimers led to successful formation of 1BODIPY?, which populated the 3BODIPY? via intersystem crossing. Among the three trimers, although very weak, only trimer 8 revealed excitation transfer to some extent. The present findings suggest that the meso-O-aryl functionalized BODIPYs due to their superior fluorescence properties are better probes to build light energy harvesting supramolecular oligomeric systems and for other applications such as sensing and imaging.

From achiral to helical bilayer self-assemblies of a 1,3,5-triazine-2,4,6-triphenol-grafted polyanionic cluster: Countercation and solvent modulation

A triazine derivative with two short alkyl chains was covalently grafted onto a disk-like polyoxometalate cluster on both sides, and an amphiphilic polyanionic cluster was obtained. The linear cluster complex showed phase separation in polar and non-polar

A Shape-Persistent Cryptand for Capturing Polycyclic Aromatic Hydrocarbons

A shape-persistent cryptand 1, containing two face-to-face oriented electron-deficient 2,4,6-triphenyl-1,3,5-triazine units separated by approximately 7 ?, and bridged by two rigid 1,8-naphthyridine linkers and a pentaethylene oxide loop, is created for c

A SUNSCREEN FORMULATION

Provided herein is synthesis of new classes of sunscreen agents, the usage of such sunscreen agents to prepare sunscreen formulation materials aiming at reduction of sunscreen agents' skin penetration. The whole purpose is to improve the biosafety of sunscreen products via novel sunscreen materials and formulation technology to reduce or to eliminate skin penetration of sunscreen agents. The technology can be applied to cosmetics, pharmaceutical or insects' repellent products.

Design and synthesis of C3-symmetric molecules containing oxepine and benzofuran moieties via Metathesis

We report a new synthetic strategy to C3-symmetric star-shaped phenyl and triazine central cores bearing oxepine and benzofuran ring systems. In this regard, we have explored the application of metathetic strategy to construct C3-sym

Triazine-cored dendritic molecules containing multiple o-carborane clusters

A series of C3-symmetricaltriazine-cored small dendritic molecules containing three to nine peripheral o-carborane clusters were synthesized through Cu(I)-catalyzedazide–alkyne cycloaddition reactions. The newly synthesized molecules containing multiple o-carborane moieties were characterized using nuclear magnetic resonance and matrix-assisted laser desorption/ionization-time of flight mass spectral analysis. The biological evaluation of these three to nine cage dendrimers was performed using breast cancer cells (Michigan Cancer Foundation 7). All these dendritic compounds showed cytotoxicity toward breast cancer cells, and the toxicity increased as the number of peripheral o-carboranes increased. The 9-cage molecule showed the highest cytotoxicity, and the half maximal inhibitory concentration (IC50) value was found to be 80.67 ng/ml. Its cytotoxicity was significantly higher than the common chemotherapy agent cisplatin. As expected, the boron-richo-carborane-appended molecules showed high thermal stability. The thermal stability increased as the number of peripheral o-carborane moieties increased.

COMPOSITION FOR FILM FORMATION, FILM, RESIST UNDERLAYER FILM-FORMING METHOD, PRODUCTION METHOD OF PATTERNED SUBSTRATE, AND COMPOUND

The composition for film formation includes a compound including a group of the formula (1) and a solvent. In the formula (1), R1 to R4 each independently represent a hydrogen atom, a monovalent organic group having 1 to 20 carbon at

Interaction of carborane-appended trimer with bovine serum albumin: A spectroscopic investigation

The interaction of symmetrical triazine-cored carborane-appended trimer 5 with bovine serum albumin has been investigated using different spectroscopic methods. The intrinsic fluorescence of BSA was quenched by the carborane trimer 5 through the dynamic q

Compound as well as preparation method and application thereof

The invention provides a compound as well as a preparation method and an application thereof. The compound is shown by the general formula (1), where X1, X2 and X3 are independently selected from formulas shown in the specification; and Y1 and Y2 are sele

Cofacial Organic Click Cage to Intercalate Polycyclic Aromatic Hydrocarbons

The synthesis of a 3-fold symmetric cofacial organic cage (COC) through Cu(I)-catalyzed azide-alkyne cycloaddition is reported. The COC can function as an efficient receptor for carcinogenic polycyclic aromatic hydrocarbons to intercalate them in its intrinsic cavity through donor-acceptor and π? π stacking interactions. The association constants (Ka) are in the range of 3.7 × 104 to 1.3 × 106 M-1. X-ray diffraction analysis authenticated that the polycyclic aromatic hydrocarbons (PAHs) are intercalated in the interior of the COC.