13960-31-1

Basic information

• Product Name: 2,4,6-tribenzyl-1,3,5-triazine
• Synonyms: 1,3,5-triazine, 2,4,6-tris(phenylmethyl)-; 2,4,6-TRIBENZYL-S-TRIAZINE
• CAS NO: 13960-31-1
• Molecular Formula: C₂₄H₂₁N₃
• Molecular Weight: 351.4436
• Mol File: 13960-31-1.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 600.2°C at 760 mmHg
• Flash Point: 266.9°C
• Density: 1.143g/cm³
• Vapor Pressure: 9.94E-14mmHg at 25°C
• Refractive Index: 1.623
• CAS DataBase Reference: 2,4,6-tribenzyl-1,3,5-triazine(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4,6-tribenzyl-1,3,5-triazine(13960-31-1)
• EPA Substance Registry System: 2,4,6-tribenzyl-1,3,5-triazine(13960-31-1)

Safety Data

• Hazardous Substances Data: 13960-31-1(Hazardous Substances Data)

Usage

General Description

2,4,6-tribenzyl-1,3,5-triazine is a chemical compound with the molecular formula C21H18N3. It is a triazine derivative that contains three benzyl groups attached to the triazine ring. 2,4,6-tribenzyl-1,3,5-triazine is commonly used as an intermediate in the synthesis of various pharmaceuticals, dyes, and agrochemicals. It exhibits strong biological activity and has been studied for its potential use as an anticancer agent. Additionally, it is also being researched for its potential use in the development of new materials, such as organic light emitting diodes (OLEDs) and liquid crystal displays (LCDs). Overall, 2,4,6-tribenzyl-1,3,5-triazine is a versatile compound with diverse potential applications in various fields.

Upstream product

• 107-10-8 propylamine 
• 140-29-4 phenylacetonitrile 

Downstream Products

• 150454-60-7 2-benzyl-4,6-bis(1-phenyl-2-morpholinoethen-1-yl)-1,3,5-triazine 
• 150454-63-0 2,4,6-Tris-((E)-1-phenyl-2-piperidin-1-yl-vinyl)-[1,3,5]triazine 
• 150454-75-4 [(E)-2-(4,6-Dibenzyl-[1,3,5]triazin-2-yl)-1,2-diphenyl-vinyl]-dimethyl-amine 
• 150454-68-5 2,4-bis(1-formyl-1-phenylmethylidene)-6-(2-morpholino-1-phenylethen-1-yl)-1,3,5-triazine 
• 150454-67-4 2-benzyl-4-(1-phenyl-2-morpholinoethen-1-yl)-6-(1-formyl-1-phenylmethyl)-1,3,5-triazine 
• 150454-69-6 [4,6-Bis-(2-oxo-1-phenyl-ethylidene)-[1,3,5]triazinan-2-ylidene]-phenyl-acetaldehyde 
• 150454-76-5 2,4-Dibenzyl-6-((E)-2-morpholin-4-yl-1,2-diphenyl-vinyl)-[1,3,5]triazine 

Relevant articles and documents

Samarium diiodide promoted synthesis of N,N′-disubstituted amidines

An efficient one-step preparation of an N,N′-disubstituted amidine by the direct nucleophilic addition of an amine to the parent nitrile using catalytic amounts of SmI2 under relatively mild conditions is developed. Alkyl, benzyl and aryl amidi

Synthesis and antibacterial activity of 2,4,6-tri substituted s-triazines

Various 2,4,6-tri substituted s-triazines were synthesized and screened for antibacterial activity against Gram-positive and Gram-negative organisms. These s-triazine derivatives displayed high in vitro antibacterial activities comparable to penicillin an