87486-36-0

Upstream product

• 79-37-8 oxalyl dichloride 
• 87486-27-9 2-cyclohexylaminoacetonitrile hydrochloride 

Downstream Products

• 98078-02-5 5-Chloro-1-cyclohexyl-3-hydrazino-1H-pyrazin-2-one 
• 98078-34-3 5-Chloro-1-cyclohexyl-3-[5-(4-methoxy-phenyl)-3-methyl-pyrazol-1-yl]-1H-pyrazin-2-one 
• 98078-33-2 3-[5-(4-Bromo-phenyl)-3-methyl-pyrazol-1-yl]-5-chloro-1-cyclohexyl-1H-pyrazin-2-one 
• 98078-32-1 5-Chloro-3-[5-(4-chloro-phenyl)-3-methyl-pyrazol-1-yl]-1-cyclohexyl-1H-pyrazin-2-one 
• 98078-31-0 5-Chloro-1-cyclohexyl-3-(3-methyl-5-phenyl-pyrazol-1-yl)-1H-pyrazin-2-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

A new synthesis of substituted 2(1H)-pyrazinones

The hydrohalides of 2-sec-aminoalkanenitriles on treatment with oxalyl halides in o-dichlorobenzene at 80-100° give 3,5-dihalo-2(1H)-pyrazinones, of which the 3-halo substituent is easily replaced by nucleophiles. A reaction mechanism for the pyrazinone s