3114-53-2

Basic information

• Product Name: 1,3,5-Triazine, 2,4-bis(4-chlorophenyl)-6-phenyl-
• CAS NO: 3114-53-2
• Molecular Formula: C21H13Cl2N3
• Molecular Weight: 378.26
• Mol File: 3114-53-2.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 1,3,5-Triazine, 2,4-bis(4-chlorophenyl)-6-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3,5-Triazine, 2,4-bis(4-chlorophenyl)-6-phenyl-(3114-53-2)
• EPA Substance Registry System: 1,3,5-Triazine, 2,4-bis(4-chlorophenyl)-6-phenyl-(3114-53-2)

Safety Data

• Hazardous Substances Data: 3114-53-2(Hazardous Substances Data)

Usage

Class

Triazine compounds

Structure

A derivative of triazine with two 4-chlorophenyl groups and one phenyl group attached to the triazine ring

Applications

a. Building block in the synthesis of various organic compounds and materials
b. Research and industrial applications in pharmaceuticals, agrochemicals, and materials science
c. Potential applications in the development of advanced materials and pharmaceuticals

Unique properties

Its structure and properties make it valuable for research and industrial applications

Chemical properties

Interesting chemical properties that may contribute to its potential applications in advanced materials and pharmaceuticals

Upstream product

• 1700-02-3 2,4-dichloro-6-phenyl-1,3,5-triazine 
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• 14401-51-5 4-chlorobenzamidine hydrochloride 
• 100-51-6 benzyl alcohol 
• 108-88-3 toluene 
• 6332-83-8 2-(4-chlorophenyl)-1-phenylethanone 

Relevant articles and documents

BENZAZOLE DERIVATIVE HAVING HETEROARYL GROUP AND ORGANIC ELECTROLUMINESCENCE DEVICE INCLUDING THE SAME

Disclosed is a benzazole derivative having a heteroaryl group, wherein the benzazole derivative having the heteroaryl group is represented by Chemical Formula 1. Also disclosed is an organic electroluminescence device including an organic layer containing

Direct oxidative coupling of amidine hydrochlorides and methylarenes: TBHP-mediated synthesis of substituted 1,3,5-triazines under metal-free conditions

Various 2,4,6-trisubstituted 1,3,5-triazines were smoothly formed via TBHP-mediated direct oxidative coupling of amidine and methylarenes. This tandem oxidation-imination-cyclization transformation exhibits a straightforward protocol to prepare 1,3,5-triazines from easily available starting materials and green oxidants under metal-free conditions.

An efficient ruthenium-catalyzed dehydrogenative synthesis of 2,4,6-triaryl-1,3,5-triazines from aryl methanols and amidines

By using [RuCl2(p-Cymene)]2/Cs2CO 3 as an efficient catalyst system, the readily available, inexpensive aryl methanols were firstly employed for dehydrogenative synthesis of aryl substituted 1,3,5-triazine derivatives. Due to the inherent stability of alcohols in contrast with aldehydes, our synthetic protocol is adaptable to a broad substrate scope, there is no need for stringent protection during the whole operation process, and it has the potential to prepare valuable products that are currently inaccessible or challenging to prepare using conventional methods. It is a significantly important complement to the conventional synthetic methodologies. This journal is the Partner Organisations 2014.