107943-25-9

Upstream product

• 31633-54-2 6-oxo-3,5-diphenyl-1,6-dihydro-as-triazine 
• 65739-54-0 3,5-diphenyl-[1,2,4]triazine 1-oxide 
• 36993-99-4 5,6-dioxo-3-phenyl-1,2,5,6-tetrahydro-as-triazine 

Downstream Products

• 132256-68-9 (3,5-Diphenyl-[1,2,4]triazin-6-yl)-phenyl-acetonitrile 
• 129190-74-5 3,5-Diphenyl-6-(2-phenylethynyl-phenoxy)-[1,2,4]triazine 
• 129190-58-5 3,5-Diphenyl-6-(2-trimethylsilanylethynyl-phenoxy)-[1,2,4]triazine 
• 129190-73-4 6-(2-Hex-1-ynyl-phenoxy)-3,5-diphenyl-[1,2,4]triazine 
• 129210-22-6 4-Butyl-1,3-diphenyl-benzo[4,5]furo[2,3-c]pyridine 
• 129190-59-6 1,3-Diphenyl-4-trimethylsilanyl-benzo[4,5]furo[2,3-c]pyridine 
• 129190-75-6 1,3,4-Triphenyl-benzo[4,5]furo[2,3-c]pyridine 
• 129190-57-4 6-(2-Iodo-phenoxy)-3,5-diphenyl-[1,2,4]triazine 
• 129190-56-3 6-methylsulfonyl-3,5-diphenyl-1,2,4-triazine 
• 129190-80-3 6-methylthio-3,5-diphenyl-1,2,4-triazine 
• 132256-58-7 6-methoxy-3,6-diphenyl-1,2,4-triazine 

Relevant academic research and scientific papers

Synthesis of 6-Substituted 3,5-diaryl-1,2,4-triazines as Potential Herbicidal Agents

A variety of 6-substituted 3,5-diaryl-1,2,4-triazines were synthesized.These diaryltriazines, which incorporate a triazine nucleus substituted by two aryl moietes, comprise a new class of bleaching herbicides.The structure-activity relationships were prov

STUDIES ON as-TRIAZINE DERIVATIVES. XV. INTRAMOLECULAR REVERSE-ELECTRON DEMAND DIELS-ALDER REACTION OF 1,2,4-TRIAZINE DERIVATIVES

5,6-Diphenyl-1,2,4-triazine-3-carboxylic acid esters which have acetylenic function in the alcoholic moiety of the ester group were converted to the pyridine derivatives condensed with lactone ring by means of intramolecular reverse electron-demand Diels-