83520-54-1

Upstream product

• 41270-66-0 2-chloro-5,6-diphenylpyrazine 
• 1588-89-2 2,3-diphenylpyrazine 
• 1489-06-1 2,3-diphenyl-5,6-dihydropyrazine 
• 61578-13-0 2,6-diphenylpyrazine 1-oxide 
• 134-81-6 benzil 

Downstream Products

• 61578-13-0 2,6-diphenylpyrazine 1-oxide 
• 106861-09-0 2,5,6-triphenylpyrazine 4-oxide 
• 109192-10-1 3-(4-Oxy-5,6-diphenyl-pyrazin-2-yl)-prop-2-yn-1-ol 
• 109192-00-9 2,3-Diphenyl-5-phenylethynyl-pyrazine 1-oxide 
• 475086-66-9 2,3-diphenyl-5-(methylamino)pyrazine 1-oxide 
• 34121-90-9 5-Methoxy-2,3-diphenyl-1,4-diazabenzene 
• 109192-06-5 5-Hex-1-ynyl-2,3-diphenyl-pyrazine 1-oxide 
• 57038-62-7 5,6-Dichloro-2,3-diphenylpyrazine 
• 96549-13-2 2,3-diphenyl-6-methylpyrazine 4-oxide 
• 156331-24-7 2,3-diphenyl-5-methoxypyrazine 1-oxide 

Relevant academic research and scientific papers

Studies on Pyrazines. Part 27. A New Deoxidative Nucleophilic Substitution of Pyrazine N-Oxides; Synthesis of Azidopyrazines with Trimethylsilyl Azide

Azidopyrazines bearing amino, methoxy and/or phenylgroups have been synthesized by reaction of pyrazine N-oxides with trimethylsilyl azide in the presence of diethylcarbamoyl chloride in refluxing acetonitrile.In most cases, the azidation occurs only at t

Syntheses and Reactions of Some 2,3-Disubstituted Pyrazine Monoxides

The reactions of 2,3-dimethyl- (4), 2,3-diphenyl- (6), and 2-methyl-3-phenyl-pyrazine monoxides (8 and 9) with phosphoryl chloride and acetic anhydride resulted in giving monochloro- and monoacetoxy-pyrazines in almost all cases.However, the reaction of 6 with acetic anhydride afforded exceptionally a diacetoxydihydropyrazine.These products were converted further to hydroxy or dichloro derivatives.