18162-28-2

Usage

Explanation

1,2,4-Triazine, 5-phenylis composed of 9 carbon atoms, 6 hydrogen atoms, and 4 nitrogen atoms.

Explanation

It has a six-membered ring containing three nitrogen atoms and three carbon atoms.

Explanation

1,2,4-Triazine, 5-phenylis used as a building block in the synthesis of various pharmaceuticals and agrochemicals.

Explanation

The compound is also utilized as a building block in the production of dyes, pigments, and polymers.

Explanation

1,2,4-Triazine, 5-phenylhas been studied for its potential biological activities, including its ability to act as an antiviral, anticancer, and antimicrobial agent.

Explanation

Due to its various applications and potential uses, 1,2,4-Triazine, 5-phenylis considered an important compound in the field of organic chemistry.

Type of Compound

Heterocyclic compound

Common Uses

Pharmaceutical and agrochemical synthesis

Applications

Dyes, pigments, and polymers production

Biological Activities

Antiviral, anticancer, and antimicrobial properties

Importance

Versatility and potential applications in organic chemistry

Upstream product

• 28735-29-7 3-hydrazino-5-phenyl-[1,2,4]triazine 
• 831218-38-3 5-Phenyl-2,5-dihydro-[1,2,4]triazine 
• 942-60-9 5-phenyl-1,2,4-triazin-3-amine 
• 72428-36-5 3-chloro-5-phenyl-1,2,4-triazine 
• 31952-61-1 5-phenyl-1,2,4-triazin-3-one 
• 72428-38-7 3-iodo-5-phenyl-1,2,4-triazine 
• 72428-37-6 3-bromo-5-phenyl-1,2,4-triazine 
• 104-85-8 para-methylbenzonitrile 

Downstream Products

• 473530-11-9 5-phenyl-3-(pyrrolidine-1-sulphonylmethyl)-1,2,4-triazine 
• 473530-09-5 5-phenyl-3-(toluene-4-sulphonylmethyl)-1,2,4-triazine 
• 473530-12-0 N,N-dimethyl-C-(5-phenyl-1,2,4-triazine)-methanesulphonamide 
• 473530-13-1 (5-phenyl-1,2,4-triazin-3-yl)-methanesulphonic acid 2,2-dimethyl-propyl ester 
• 473530-14-2 5-phenyl-3-(1-phenylsulphonyl-hex-5-ynyl)-1,2,4-triazine 
• 473530-10-8 3-(morpholine-4-sulphonylmethyl)-5-phenyl-1,2,4-triazine 
• 473530-18-6 1-(5-phenyl-1,2,4-triazin-3-yl)-hex-5-yne-1-sulphonic acid dimethylamide 
• 473530-19-7 1-(5-phenyl-1,2,4-triazin-3-yl)-hex-5-yne-1-sulphonic acid 2,2-dimethylpropyl ester 
• 473530-15-3 5-phenyl-3-[1-(toluene-4-sulphonyl)-hex-5-ynyl]-1,2,4-triazine 
• 473530-17-5 5-phenyl-3-[1-(pyrrolidine-4-sulphonyl-hexyl)-5-ynyl]-1,2,4-triazine 
• 473530-16-4 3-[1-(morpholine-4-sulphonyl)-hex-5-ynyl]-5-phenyl-1,2,4-triazine 
• 21134-91-8 5,6-diphenyl-1,2,4-triazine 
• 64494-09-3 3-(4-methoxyphenyl)-5,6-diphenyl-1,2,4-triazine 

Relevant academic research and scientific papers

PREPARATION OF METAL-PYRIDINE DERIVATIVE COMPLEXES FOR USE IN MEDICAL IMAGING

The present invention relates to methods of forming metal-pyridine derivative complexes using pericyclic reactions with metal-1,2,4- triazine derivative complexes and a dienophile as the reactants. The reactants are bioorthogonal and the methods are parti

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.

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

Ring Transformations and Amination in Reactions of 3-Halogeno-5-phenyl-1,2,4-triazines with Potassium Amide in Liquid Ammonia

The reactions of 3-X-5-phenyl-1,2,4-triazines (X = fluoro, chloro, bromo, iodo) toward potassium amide/liquid ammonia were studied.Whereas the 3-fluoro compound gives only the 3-amino derivative, the 3-chloro, 3-bromo, and 3-iodo compounds yield a complex mixture containing, besides 3-amino-5-phenyl-1,2,4-triazine and 5-phenyl-1,2,4-triazine, ring transformation products, i.e., 3,5-diphenyl-1,2,4-triazine, 2,4-diphenyl-1,3,5-triazine, 6-amino-2,4-diphenyl-1,3,5-triazine, and 3-X-5-phenyl-1,2,4-triazole.Evidence is found that in the ring transformation of 3-X-5-phenyl-1,2,4-triazines into 2,4-diphenyl-1,3,5-triazines, benzamidine must be an intermediate.The mechanisms of the amination and ring transformation are extensively discussed.