21134-91-8

Usage

Uses

Used in Pharmaceutical Industry:
5,6-DIPHENYL-1,2,4-TRIAZINE is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique structure allows for the development of drug candidates with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, 5,6-DIPHENYL-1,2,4-TRIAZINE serves as a crucial building block for the creation of novel agrochemicals, contributing to the development of more effective and environmentally friendly pesticides and herbicides.
Used in Materials Science:
5,6-DIPHENYL-1,2,4-TRIAZINE is utilized as a component in the synthesis of advanced materials with specific properties, such as high thermal stability and unique optical characteristics, for applications in various industries.
Used as a Fluorescence Probe:
5,6-DIPHENYL-1,2,4-TRIAZINE has been studied for its potential as a fluorescence probe, which can be employed in various analytical techniques to detect and quantify specific substances.
Used as a Photoinitiator:
In the field of polymer chemistry, 5,6-DIPHENYL-1,2,4-TRIAZINE is used as a photoinitiator to trigger the polymerization process upon exposure to light, enabling the fabrication of polymeric materials with tailored properties.
Used as an Electron Transporting Material:
5,6-DIPHENYL-1,2,4-TRIAZINE has been explored for its potential as an electron transporting material in organic electronic devices, such as organic light-emitting diodes (OLEDs) and organic solar cells, due to its unique electronic properties.

InChI:InChI=1/C15H11N3/c1-3-7-12(8-4-1)14-15(18-17-11-16-14)13-9-5-2-6-10-13/h1-11H

Upstream product

• 4512-00-9 5,6-diphenyl-1,2,4-triazin-3(2H)-one 
• 21383-24-4 (5,6-diphenyl-[1,2,4]triazin-3-yl)-hydrazine 
• 103744-55-4 benzenesulfonic acid-[N'-(5,6-diphenyl-[1,2,4]triazin-3-yl)-hydrazide] 
• 4511-99-3 5,6-diphenyl-1,2,4-triazine-3-amine 
• 121733-38-8 2,3-Dihydro-5,6-diphenyl-1,2,4-triazin-4-oxid 
• 116178-10-0 1,6-dihydro-5,6-diphenyl-as-triazine 
• 134-81-6 benzil 
• 18162-28-2 5-phenyl-1,2,4-triazine 
• 831218-38-3 5-Phenyl-2,5-dihydro-[1,2,4]triazine 
• 121754-93-6 Benzil-(Z)-hydrazon-(E)-oxim 
• 34177-11-2 3-chloro-5,6-diphenyl-1,2,4-triazine 
• 35883-52-4 5,6-diphenyl-[1,2,4]triazine-3-carboxylic acid ethyl ester 

Downstream Products

• 390401-03-3 3-(2-Bromo-α-hydroxybenzyl)-5,6-diphenyl-1,2,4-triazine 
• 64494-09-3 3-(4-methoxyphenyl)-5,6-diphenyl-1,2,4-triazine 
• 116089-61-3 N-(2,3-Diphenyl-pyridin-4-yl)-N,N'-dimethyl-ethane-1,2-diamine 
• 116089-62-4 N-(5,6-Diphenyl-pyridin-3-yl)-N,N'-dimethyl-ethane-1,2-diamine 
• 153783-42-7 6-Methoxy-2,3-diphenylpyrrolo<1,2-b><1,2,4>triazin 
• 151724-27-5 3,4-diphenyl-6,7-dihydro-5H-[2]pyrindine 
• 390401-11-3 5,6-Diphenyl-3-[2-(trimethylsilylethynyl)benzoyl]-1,2,4-triazine 
• 390401-15-7 2,3-Diphenyl-4-trimethylsilyl-1-azafluorenone 
• 390401-07-7 3-(2-Bromobenzoyl)-5,6-diphenyl-1,2,4-triazine 

Relevant academic research and scientific papers

Novel one pot synthesis of substituted 1,2,4-triazines

Substituted-1,2,4-triazines were conveniently prepared in one pot by the condensation of amides and 1,2-diketones in presence of base, followed by cyclisation with hydrazine hydrate.

Deamination of 2-aminothiazoles and 3-amino-1,2,4-triazines with nitric oxide in the presence of a catalytic amount of oxygen

2-Aminothiazoles, 2-aminobenzazoles, and 3-amino-1,2,4-triazines were deaminated using nitric oxide (NO) in the presence of a catalytic amount of oxygen to afford corresponding unsubstituted heterocycles in good yields.

Synthesis of Isoquinolines by Cycloaddition of Arynes to 1,2,4-Triazines

Benzyne has been generated from benzenediazonium-2-carboxylate in the presence of several 1,2,4-triazines 1 and isoquinolines 2 have been isolated in moderate yield. 1-Aminobenzotriazole was also used as the source of benzyne and isoquinolines were again isolated in moderate yield from these reactions. 4-Methylbenzyne, which was generated from 5-methylanthranilic acid, reacted unselectively with the triazines to give mixtures of 6- and 7-methylisoquinolines 3 and 4.On the other hand reactions of 3-methylbenzyne with the triazines 1d and 1e proceeded with high regioselectivity, giving only the 5-methylisoquinoline 5a and the 8-methylisoquinoline 6b, respectively.

The Configuration of 1,2-Diketone Hydrazone Oximes

The configuration of 1,2-diketone (Z)-hydrazone (E)-oximes 3a-c was determined by ring closure with formaldehyde to 1,2,4-triazine 4-oxides 5a-c and the tautomeric 4-hydroxy-1,2,4-triazines 6a-c and by Beckmann reaction to 1,2,4 triazoles 8a-c.From benzil

STUDIES ON as-TRIAZINE DERIVATIVES. X. ADDITION REACTION OF PHENYLMAGNESIUM BROMIDE WITH 1,2,4-TRIAZINES

The reaction of 1,2,4-triazine with phenylmagnesium bromide was investigated.Every position 3,5, and 6 in a 1,2,4-triazine ring is active in the addition reaction of Grignard reagents.Since 5-phenyl-1,2,4-triazine, 5,6-diphenyl-1,2,4-triazine, and 3,5,6-t