3140-75-8

Basic information

• Product Name: Benzaldehyde, 4,4',4''-[1,3,5-triazine-2,4,6-triyltris(oxy)]tris-
• Synonyms: Benzaldehyde, 4,4',4''-[1,3,5-triazine-2,4,6-triyltris(oxy)]tris-;4-[[4,6-bis(4-formylphenoxy)-1,3,5-triazin-2-yl]oxy]benzaldehyde
• CAS NO: 3140-75-8
• Molecular Formula: C₂₄H₁₅N₃O₆
• Molecular Weight: 441.3924
• Mol File: 3140-75-8.mol
• Article Data: 25

Chemical Properties

• Melting Point: 174-176 °C(Solv: ethyl acetate (141-78-6))
• Boiling Point: 700.5±70.0 °C(Predicted)
• Appearance: /
• Density: 1.397±0.06 g/cm3(Predicted)
• PKA: -0.73±0.10(Predicted)
• CAS DataBase Reference: Benzaldehyde, 4,4',4''-[1,3,5-triazine-2,4,6-triyltris(oxy)]tris-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzaldehyde, 4,4',4''-[1,3,5-triazine-2,4,6-triyltris(oxy)]tris-(3140-75-8)
• EPA Substance Registry System: Benzaldehyde, 4,4',4''-[1,3,5-triazine-2,4,6-triyltris(oxy)]tris-(3140-75-8)

Safety Data

• Hazardous Substances Data: 3140-75-8(Hazardous Substances Data)

Usage

General Description

Benzaldehyde, 4,4',4''-[1,3,5-triazine-2,4,6-triyltris(oxy)]tris- is a chemical compound that consists of a benzaldehyde group and a 1,3,5-triazine-2,4,6-triyltris(oxy) group. It is commonly used in the synthesis of various organic compounds, including pharmaceuticals, dyes, and perfumes. Benzaldehyde, 4,4',4''-[1,3,5-triazine-2,4,6-triyltris(oxy)]tris- is known for its aromatic almond-like odor and is often used as a flavoring agent in food products. It also has applications in the manufacturing of polymers and resins. Additionally, it has been studied for its potential medical and biological properties, particularly in the field of cancer treatment and drug delivery systems.

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

• 120971-26-8 tris-[4-(4-oxo-2-thioxo-thiazolidin-5-ylidenemethyl)-phenoxy]-[1,3,5]triazine 
• 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 

Relevant articles and documents

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

Synthesis of a New Trialdehyde Template for Molecular Impriting

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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

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

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

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.