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

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

Uses

Used in Pharmaceutical Industry:
2,4,6-tribenzyl-1,3,5-triazine is used as an intermediate in the synthesis of various pharmaceuticals. Its unique structure and properties make it a valuable component in the development of new drugs.
Used in Dye Industry:
In the dye industry, 2,4,6-tribenzyl-1,3,5-triazine is used as a key intermediate for the production of various dyes. Its chemical properties contribute to the color and stability of the dyes.
Used in Agrochemical Industry:
2,4,6-tribenzyl-1,3,5-triazine is utilized as an intermediate in the synthesis of agrochemicals, such as pesticides and herbicides. Its presence in these compounds can enhance their effectiveness and selectivity.
Used in Anticancer Applications:
2,4,6-tribenzyl-1,3,5-triazine is being studied for its potential use as an anticancer agent. Its strong biological activity suggests that it may play a role in inhibiting cancer cell growth and proliferation.
Used in Material Science:
2,4,6-tribenzyl-1,3,5-triazine is being researched for its potential use in the development of new materials, such as organic light emitting diodes (OLEDs) and liquid crystal displays (LCDs). Its chemical properties may contribute to the performance and efficiency of these advanced materials.

Upstream product

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

Downstream Products

• 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 
• 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 

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

Cyclotrimerization of nitriles catalyzed by SmI2/amines: Synthesis of 2,4,6-trisubstituted-s-triazines

SmI2 has been found to catalyze a reaction of cyclotrimerization of nitriles in the presence of amine as cocatalyst to give 2,4,6-trisubstituted- s-triazines effectively under mild reaction conditions. The yield depends on the structure of nitriles.

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