3140-75-8

Usage

Uses

Used in Pharmaceutical Industry:
Benzaldehyde, 4,4',4''-[1,3,5-triazine-2,4,6-triyltris(oxy)]trisis utilized as a key intermediate in the synthesis of pharmaceuticals. Its unique structure allows it to be a building block for the development of new drugs, particularly those targeting specific medical conditions.
Used in Flavoring and Fragrance Industry:
Leveraging its distinctive almond-like odor, Benzaldehyde, 4,4',4''-[1,3,5-triazine-2,4,6-triyltris(oxy)]trisis employed as a flavoring agent in food products. It enhances the taste and aroma of various consumables, contributing to the overall sensory experience.
Used in Dye and Perfume Industry:
Benzaldehyde, 4,4',4''-[1,3,5-triazine-2,4,6-triyltris(oxy)]trisis also used in the creation of dyes and perfumes, where its aromatic properties are harnessed to produce a range of scents and colors for different applications.
Used in Polymer and Resin Manufacturing:
Benzaldehyde, 4,4',4''-[1,3,5-triazine-2,4,6-triyltris(oxy)]trisis incorporated into the production of polymers and resins, where it contributes to the development of materials with specific properties required for various end-use applications.
Used in Cancer Treatment and Drug Delivery Research:
Benzaldehyde, 4,4',4''-[1,3,5-triazine-2,4,6-triyltris(oxy)]trishas been studied for its potential in medical and biological fields, particularly in cancer treatment and drug delivery systems. Its unique chemical structure offers opportunities for the development of novel therapeutic approaches and targeted drug delivery mechanisms.

Upstream product

• 108-77-0 1,3,5-trichloro-2,4,6-triazine 
• 123-08-0 4-hydroxy-benzaldehyde 
• 22666-84-8 4-hydroxybenzaldehyde sodium salt 

Downstream Products

• 1269441-03-3 C₃₀H₂₁N₁₅O₃ 
• 1269441-04-4 C₃₆H₃₃N₁₅O₃ 
• 1269441-05-5 C₃₆H₃₃N₁₅O₉ 
• 1370510-98-7 2,2',2''-[1,3,5-triazine-2,4,6-triyltris(oxy-4,1-phenylene)]tris[6-(4-nitrophenyl)-4-phenyl-1,3-diazabicyclo[3.1.0]hex-3-ene] 
• 1363379-34-3 2,4,6-tris[4-{(E)-[2'-(4-fluorophenylcarbonyl)hydrazinylidene]methyl}phenoxy]-1,3,5-triazine 
• 1363379-36-5 2,4,6-tris[4-{(E)-[2'-(4-methoxyphenylcarbonyl)hydrazinylidene]methyl}phenoxy]-1,3,5-triazine 
• 1363379-31-0 2,4,6-tris[4-{(E)-[2'-(phenylcarbonyl)hydrazinylidene]methyl}phenoxy]-1,3,5-triazine 
• 1363379-35-4 2,4,6-tris[4-{(E)-[2'-(4-hydroxyphenylcarbonyl)hydrazinylidene]methyl}phenoxy]-1,3,5-triazine 
• 1363379-33-2 2,4,6-tris[4-{(E)-[2'-(4-chlorophenylcarbonyl)hydrazinylidene]methyl} phenoxy]-1,3,5-triazine 
• 1363379-39-8 2,4,6-tris[4-{(E)-[2'-(4-nitrophenylcarbonyl)hydrazinylidene]methyl}phenoxy]-1,3,5-triazine 
• 1363379-38-7 2,4,6-tris[4-{(E)-[2'-(4-methylphenylcarbonyl)hydrazinylidene]methyl}phenoxy]-1,3,5-triazine 
• 1363379-40-1 2,4,6-tris[4-{(E)-[2'-(4-aminophenylcarbonyl)hydrazinylidene]methyl}phenoxy]-1,3,5-triazine 
• 1363379-32-1 2,4,6-tris[4-{(E)-[2'-(4-bromophenylcarbonyl)hydrazinylidene]methyl}phenoxy]-1,3,5-triazine 
• 1476769-12-6 2,4,6-tris[4'-{1''-(phenyl)-2''-propenone-3''-yl}phenoxy]-1,3,5-triazine 

Relevant academic research and scientific papers

Synthesis and characterization of a novel fluorene-based covalent triazine framework as a chemical adsorbent for highly efficient dye removal

Covalent organic frameworks (COFs) are known as emerging candidates for textile wastewater treatment due to their high porosity and regular channel structure. In the current paper, a Fluorene-based COF (FLU-COF) was synthesized by a facile method directin

A dual-functionalized, luminescent and highly crystalline covalent organic framework: Molecular decoding strategies for VOCs and ultrafast TNP sensing

Luminescent and robust covalent organic frameworks (COFs) with desired crystallinity and properties are rarely obtained due to synthetic challenges in combining the molecular building blocks required to adopt a structure that prevents aggregation-caused q

Synthesis and evaluation of biological activities of tripodal imines and β-lactams attached to the 1,3,5-triazine nucleus

Abstract: A novel collection of tripodal β-lactam derivatives with 1,3,5-triazine as the central core is presented for the first time. The diastereoselective synthesis of tris-β-lactams was achieved via a [2 + 2] cycloaddition reaction between s-triazine-

Covalent triazine-based polyimine framework as a biocompatible pH-dependent sustained-release nanocarrier for sorafenib: An in vitro approach

In the present study, a novel polyimine-based covalent triazine framework (PI-CTF) was introduced as a promising biocompatible carrier for sorafenib (SFN) delivery. High specific surface area and porosity allowed us to achieve drug loading and encapsulati

Synthesis of novel star-shaped molecules based on a 1,3,5-triazine core linked to different heterocyclic systems as novel hybrid molecules

The synthesis of novel star-shaped compounds based on an s-triazine core and linked to hexahydroacridinediones, pyrimido[4,5-b]quinolones, 1H-isoquinolino[2,1-a]quinolines, tetrahydro-4H-chromenes, dihydropyrano[2,3-c]pyrazoles, thiazole, or benzothiazole

The synthesis and characterization of [M(salen/salophen/saldeta)] [M=Cr(III), Mn(III) or Fe(III)] capped s-triazine cored tripodal trinuclear Schiff bases complexes

Abstract: Ligand complexes ([M(salen/salophen)]2O, [M(saldeta)]Cl shortened as LC, M=Cr(III), Mn(III) or Fe(III)), have been synthesized. 2,4,6-tris(4-formylphenoxy)-1,3,5-triazine (3) was synthesized with the reaction of p-hydroxybenzaldehyde

Construction of Flexible Amine-linked Covalent Organic Frameworks by Catalysis and Reduction of Formic Acid via the Eschweiler–Clarke Reaction

Compared to the current mainstream rigid covalent organic frameworks (COFs) linked by imine bonds, flexible COFs have certain advantages of elasticity and self-adaptability, but their construction and application are greatly limited by the complexity in s

Luminescent Triazene-Based Covalent Organic Frameworks Functionalized with Imine and Azine: N2 and H2 Sorption and Efficient Removal of Organic Dye Pollutants

Design of adsorbents with high stability and efficiency to achieve rapid uptake and high capacity for dye pollutants is a key challenge in environmental remedies. Herein, we have design and synthesized three triazene-based imine and azine functionalized c

Post-synthetic Modification of Covalent Organic Frameworks through in situ Polymerization of Aniline for Enhanced Capacitive Energy Storage

Covalent organic frameworks (COFs) having layered architecture with open nanochannels and high specific surface area are promising candidates for energy storage. However, the low electrical conductivity of two-dimensional COFs often limits their scope in

A Synergistic Magnetically Retrievable Inorganic-Organic Hybrid Metal Oxide Catalyst for Scalable Selective Oxidation of Alcohols to Aldehydes and Ketones

Herein, we report a synergistic silica coated magnetic Fe3O4 catalyst functionalized with nitrogen rich organic moieties and immobilized with cobalt metal ion (FNP-5) for selective oxidation of alcohols to aldehydes and ketones using tert-butyl hydroperoxide (TBHP) as oxidant. The catalyst was rigorously characterized via several techniques which delineate its core-shell structure, magnetic behavior, phase and crystal structure. The Co(III) acts as the active catalytic center for selective oxidation reaction. The control reactions revealed radical mechanistic pathway assisted by the synergism induced by the inorganic-organic hybrid nature of FNP-5. The other features of current protocol involve neat reaction conditions, high TOF values, scalability of product and low E-factor value (1.92). Moreover, FNP-5 could be effortlessly separated via an external magnet, displays recyclability over eight catalytic cycles and exhibits structural integrity even after rigorous use. Overall, these results manifest the understanding of synergistic architectures as sustainable surrogates for selective oxidation reactions.