119426-64-1

Upstream product

• 2835-06-5 phenylglycin 
• 131705-96-9 N-(2-nitro-4-acetylphenyl)phenylglycine 
• 131705-97-0 1,2-dihydro-2-phenyl-6-acetylquinoxalin-3(4H)one 
• 131705-99-2 6-acetyl-3-chloro-2-phenylquinoxaline 
• 131705-98-1 6-acetyl-2-phenylquinoxalin-3(4H)one 
• 18640-58-9 3-nitro-4-bromoacetophenone 
• 131706-00-8 6-acetyl-2-phenyl-1,2,3,4-tetrahydroquinoxaline 
• 1074-12-0 phenylglyoxal hydrate 
• 21304-39-2 1-(3,4-diaminophenyl)ethanone 

Downstream Products

• 131706-06-4 1-(4-Oxy-2-phenyl-quinoxalin-6-yl)-ethanone oxime 
• 119426-39-0 5-Methyl-5-(2'-phenyl-quinoxalin-6'-yl)-imidazolidine-2,4-dione 
• 131706-00-8 6-acetyl-2-phenyl-1,2,3,4-tetrahydroquinoxaline 
• 131706-05-3 1-(4-Oxy-2-phenyl-quinoxalin-6-yl)-ethanone 
• 131706-01-9 methyl-(2-phenylquinoxalin-6-yl)ketoxime 

Relevant academic research and scientific papers

2-Phenyl-(6(7)-R-substituted quinoxalines N-oxides. Synthesis, structure elucidation and antimicrobial activity

A certain number of isomeric 2-phenylquinoxalines N-oxides bearing substituents at position 6/7 were prepared in order to investigate anti-microbial activity. The effect of some electron-withdrawing groups seem to increase an anti-Trichomonas vaginalis ac