109854-55-9

Upstream product

• 60855-47-2 3-Chloro-4-methyl-6-p-tolyl-pyridazine 
• 17356-08-0 thiourea 
• 70420-98-3 6-p-Tolyl-3(2H)-pyridazinethione 
• 74-88-4 methyl iodide 
• 21004-61-5 4-methyl-6-p-tolyl-2H-pyridazin-3-one 

Downstream Products

• 109854-60-6 4-Methyl-2-piperidin-1-ylmethyl-6-p-tolyl-2H-pyridazine-3-thione 
• 120317-60-4 4-Methyl-4-phenyl-6-p-tolyl-4,5-dihydro-2H-pyridazine-3-thione 
• 120317-61-5 4-Methyl-4,6-di-p-tolyl-4,5-dihydro-2H-pyridazine-3-thione 
• 120317-59-1 4,4-Dimethyl-6-p-tolyl-4,5-dihydro-2H-pyridazine-3-thione 
• 109854-68-4 4-Methyl-3-methylsulfanyl-6-p-tolyl-pyridazine 
• 109854-66-2 C₂₄H₂₂N₄S₂ 
• 109854-69-5 3-ethylthio-4-methyl-6-p-tolylpyridazine 

Relevant academic research and scientific papers

Action of Grignard Reagents on 6-Arylpyridazin-3(2H)-thiones

6-Arylpyridazin-3(2H)-thiones (1a-c) react with Grignard reagents by 1,4-addition to give either 4-substituted 6-aryl-4,5-dihydropyridazin-3(2H)-thiones (2a-c) or their dehydrogenated products, namely 4-substituted 6-arylpyridazin-3(2H)-thiones (3d-k).The

Tautomerism in 6-Arylpyridazin-3(2H)-thiones and Some of Their Reactions

6-Arylpyridazin-3(2H)-thiones exist mainly, if not entirely, in the thione form (1).This was shown by spectroscopic studies on some of these compounds and their substitution products either on the nitrogen or on the sulphur in the mercaptopyridazine form