1186331-38-3

Upstream product

• 1186331-36-1 5-(2,6-dimethoxyphenyl)-3-(methylsulfanyl)-1,2,4-triazine 

Downstream Products

• 1186331-43-0 benzyl {1-[5-(2,6-dimethoxyphenyl)-1,2,4-triazin-3-yloxy]but-3-yn-2-yl}carbamate 
• 1186331-44-1 benzyl {1-[5-(2,6-dimethoxyphenyl)-1,2,4-triazin-3-yloxy]pent-4-yn-2-yl}carbamate 
• 1222866-80-9 2-(5-(2,6-dimethoxyphenyl)-1,2,4-triazin-3-ylthio)-N,N-dimethylethanamine 
• 1222866-85-4 2-(5-(2,6-dimethoxyphenyl)-1,2,4-triazin-3-yloxy)-N,N-dimethylethanamine 
• 1222866-99-0 5-(2,6-dimethoxyphenyl)-3-vinyl-1,2,4-triazine 

Relevant academic research and scientific papers

SAR studies on new bis-aryls 5-HT7 ligands: Synthesis and molecular modeling

Structure-activity relationships of a series of bis-arylic compounds, investigated as 5-HT7R ligands, are reported. The main structural modifications involved a central aryl moiety (phenyl, pyridine, diazine, triazine) and the nature and positi

Synthesis of 3-amlno-8-azachromans and 3-amino-7-azabenzofurans via inverse electron demand dlels-alder reaction

The synthesis of 3-amino-8-azachromans and 3-amino-7-azabenzofurans derivatives is reported. The synthetic strategy is based on an inverse electron demand Diels-Alder approach, which employs 1,2,4-triazines that are judiciously substituted with amino alkynols. This approach permits the variation of the substituent on the aromatic core and on the amine moiety, as well as of the size of the nonaromatic ring.