130879-25-3

Upstream product

• 79-37-8 oxalyl dichloride 

Downstream Products

• 106718-99-4 Dimethyl 2,6-dichloro-pyridine-3,4-dicarboxylate 
• 130879-34-4 Dimethyl 3-chloro-1-paramethoxyphenyl-2(1H)-pyridone-4,5-dicarboxylate 
• 130879-36-6 Dimethyl 3-methoxy-1-paramethoxyphenyl-2(1H)-pyridone-4,5-dicarboxylate 
• 1380294-86-9 5-chloro-3-((2-iodophenyl)amino)-1-(4-methoxyphenyl)pyrazin-2(1H)-one 
• 1380294-85-8 1-benzyl-5-chloro-3-((4-chloro-2-iodophenyl)amino)pyrazin-2(1H)-one 
• 1380294-88-1 5-chloro-3-((2-iodo-4-methylphenyl)amino)-1-(4-methoxyphenyl)pyrazin-2(1H)-one 
• 1380295-07-7 5-chloro-1-(4-methoxyphenyl)-3-((2-(p-tolylethynyl)phenyl)amino)pyrazin-2(1H)-one 
• 1380294-90-5 5-chloro-3-(2-iodo-4-(trifluoromethyl)phenylamino)-1-(4-methoxyphenyl)pyrazin-2(1H)-one 
• 1394231-15-2 dimethyl 2-(6-chloro-4-(4-methoxyphenyl)-3-oxo-3,4-dihydropyrazin-2-yl)malonate 
• 1394231-07-2 diethyl 2-(6-chloro-4-(4-methoxyphenyl)-3-oxo-3,4-dihydropyrazin-2-yl)malonate 
• 1415565-55-7 5-chloro-7-(4-methoxyphenyl)-3-methylimidazo[1,2-a]pyrazin-8(7H)-one 
• 1415565-74-0 C₁₄H₁₂ClN₃O₂ 
• 1415565-75-1 7-(4-methoxyphenyl)-3-methyl-5-p-tolylimidazo[1,2-a]pyrazin-8(7H)-one 
• 1415565-76-2 7-(4-methoxyphenyl)-3-methyl-5-phenylimidazo[1,2-a]pyrazin-8(7H)-one 

Relevant academic research and scientific papers

Synthesis and fungicidal activity of 3,5-dichloropyrazin-2(1H)-one derivatives

We synthesized a family of 3,5-dichloropyrazin-2(1H)-one derivatives and assessed their in vitro fungicidal activity against Candida albicans. Compounds 11 and 20 were most active against C. albicans and induced accumulation of reactive oxygen species in