22285-41-2

Upstream product

• 22278-80-4 4-amino-6-benzyl-3-mercapto-1,2,4-triazine-5(4H)-one 
• 74-88-4 methyl iodide 
• 156-06-9 2-oxo-3-(phenyl)propionic acid 
• 67-56-1 methanol 
• 124-41-4 sodium methylate 
• 881-90-3 4-benzylidene-2-methyl-2-oxazolin-5-one 

Downstream Products

• 1373439-72-5 4-amino-6-benzyl-3-(2-benzylidenehydrazinyl)-1,2,4-triazin-5(4H)-one 
• 1373439-74-7 4-amino-6-benzyl-3-(2-(4-methoxybenzylidene)hydrazinyl)-1,2,4-triazin-5(4H)-one 
• 1373440-59-5 4-amino-6-benzyl-3-(2-(3,4,5-trimethoxybenzylidene)hydrazinyl)-1,2,4-triazin-5(4H)-one 
• 1373439-77-0 4-amino-6-benzyl-3-(2-(4-hydroxybenzylidene)hydrazinyl)-1,2,4-triazin-5(4H)-one 
• 1373439-80-5 4-amino-6-benzyl-3-(2-(4-nitrobenzylidene)hydrazinyl)-1,2,4-triazin-5(4H)-one 
• 1373439-83-8 4-amino-6-benzyl-3-(2-(1-phenylethylidene)hydrazinyl)-1,2,4-triazin-5(4H)-one 
• 1373439-89-4 4-amino-6-benzyl-3-(2-(1-(4-chlorophenyl)ethylidene)hydrazinyl)-1,2,4-triazin-5(4H)-one 
• 1373439-94-1 4-amino-6-benzyl-3-(2-(1-p-tolylethylidene)hydrazinyl)-1,2,4-triazin-5(4H)-one 
• 1373439-99-6 4-amino-6-benzyl-3-(2-(1-(pyridin-2-yl)ethylidene)hydrazinyl)-1,2,4-triazin-5(4H)-one 
• 1373440-03-9 4-amino-6-benzyl-3-(2-(1-(furan-2-yl)ethylidene)hydrazinyl)-1,2,4-triazin-5(4H)-one 
• 1373440-08-4 2-acetyl-8-(N,N-diacetylamino)-6-benzyl-7-oxo-3-phenyl-2,3-dihydro-7H-[1,2,4] triazolo[4,3-b][1,2,4]triazine 
• 1373440-13-1 2-acetyl-8-(N,N-diacetylamino)-6-benzyl-3-(4-methoxyphenyl)-7-oxo-2,3-dihydro-7H-[1,2,4]triazolo[4,3-b][1,2,4]triazine 
• 1373440-17-5 2-acetyl-8-(N,N-diacetylamino)-3-(4-chlorophenyl)-6-(4-methoxybenzyl)-3-methyl-7-oxo-2,3-dihydro-7H-[1,2,4]triazolo[4,3-b][1,2,4]triazine 
• 1373440-19-7 2-acetyl-8-(N,N-diacetylamino)-6-(4-methoxybenzyl)-3-methyl-7-oxo-3-p-tolyl-2,3-dihydro-7H-[1,2,4]triazolo[4,3-b][1,2,4]triazine 

Relevant academic research and scientific papers

Synthesis and Acaricidal Activity of Some New 1,2,4-Triazine Derivatives

A new series of 1,2,4-triazine derivatives were designed, synthesized, and identified on the basis of IR, 1H-NMR, 13C-NMR, and EI-MS spectral data. The potent acaricidal activity of 1,2,4-triazine derivatives against eggs and adult female of Tetranychus urticae (Koch) was assessed compared with pyridaben under laboratory conditions. Structure acaricidal activity relationships of the promising 1,2,4-triazine derivatives were analyzed for eggs and adult female; the nature and position of the substituents were important in demonstration of the activities.

Synthesis of some novel 6-benzyl(or substituted benzyl)-2-β-D- glucopyranosyl-1,2,4-triazolo[4,3-b][1,2,4]triazines as potential antimicrobial chemotherapeutics

Glucosidation of the new 8-amino-6-benzyl(or substituted benzyl)-2,8-dihydro-1,2,4-triazolo[4,3-b][1,2,4]triazin-7(3H)-ones (3a-d) with 2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl bromide 4 gave the corresponding N-glucosides 5a-d. Chemical transformations

Derivatives of 1,2,4-Triazin-5-one

3-Mercapto-1,2,4-triazin-5-ones were obtained by the reaction of thiosemicarbazide with α-keto carboxylic acids, 2-cyano-2-propanol, isatin, and 5-furfurylidenethiazolidine-2,4-dione.The first three methods gave high yields.

Herbicidal agents

3-[HYDROGEN-, (UNSUBSTITUTED AND HALO, AMINO, NITRO, ALKYL, ALKANOYL, ALKOXY, ALKYLMERCAPTO, ARYLOXY AND/OR ARYL-MERCAPTO-SUBSTITUTED) ALIPHATIC-, CYCLOALIPHATIC-, ARALIPHATIC-, ARYL-, OR HETEROCYCLIC- -SUBSTITUTED OXY, MERCAPTO OR AMINO]4-[AMINO; MONO AND DI (UNSUBSTITUTED AND CYANO, HYDROXY AND/OR HALO-SUBSTITUTED) ALKYL- AND/OR ALKANOYL-AMINO; N-heterocyclic; or N-(unsubstituted and aryl, haloaryl, alkoxyaryl, nitroaryl and/or heterocyclic- substituted) alkylidene or cycloalkylidene]-6-[(unsubstituted and halo, nitro, carbo lower alkoxy, alkyl, alkoxy, alkylmercapto, aralkylmercapto, aryloxy and/or arylmercapto-substituted) aliphatic, cycloaliphatic, araliphatic, aryl, or heterocyclic]-1,2,4-triazine-5-ones, which possess herbicidal properties, and which may be produced by conventional methods.