94243-24-0

Upstream product

• 24108-40-5 3-phenyl-1,2,4-triazine 
• 94243-20-6 1-(3-phenyl-1,2,4-triazin-5-yl)ethanone oxime 

Downstream Products

• 59576-29-3 methyl(2-phenylpyridin-6-yl)-methanone 
• 496935-66-1 C₁₈H₁₇N₅ 

Relevant academic research and scientific papers

Reinvestigation of the reaction of 3-substituted 1,2,4-triazines with nitronate anions: unexpected behavior of 3-(2-ethoxyphenyl)-1,2,4-triazine in the reaction with anions of nitroalkanes

[Figure not available: see fulltext.] 3-Substituted 1,2,4-triazines easily react with nitronate anions to replace hydrogen atom in the position C-5 according to nucleophilic substitution mechanism and form appropriate oximes of 5-formyl- or 5-acyl-1,2,4-t

Synthesis and biological activity evaluation of Schiff bases of 5-acyl-1,2,4-triazine

A simple and general method has been developed for the synthesis of various Schiff bases (oximes, hydrazones, semicarbazones and thiosemicarbazones) derived from 5-acyl-1,2,4-triazines. Some of the new synthesized Schiff bases were tested for biological a

Antiviral activity evaluation of pyrazolo[4,3-e][1,2,4]triazines

The main purpose of this study is to screen synthesized pyrazolo[4,3- e][1,2,4]triazine derivatives for their antiviral activity against a panel of DNA and RNA viruses. Minimum cytotoxic and minimum virus-inhibitory concentrations of these compounds were

Enantioselective reduction of 5-acyl-1,2,4-triazines and their oximes by baker's yeast [1]

Variously substituted 5-acyl-1,2,4-triazines 4a-d were regioselectively synthesized through a sequence involving nucleophilic acylation of 1,2,4-triazines 1a-b with nitronate anions 2a-c followed by hydrolysis of the oximes 3a-d thus formed, by sodium hyd

REACTION OF 1,2,4-TRIAZINES WITH NITRONATE ANIONS, DIRECT NUCLEOPHILIC ACYLATION OF 1,2,4-TRIAZINES

Nitronate anions replace 5-hydrogen atom in a variety of 3-substituted 1,2,4-triazine derivatives giving oximes of 5-formyl and 5-acyl 1,2,4-triazines.