201735-12-8

Upstream product

• 614-16-4 Benzoylacetonitrile 
• 18440-58-9 1-(N-phenylhydrazono)-1-chloropropanone 

Downstream Products

• 1426835-33-7 3-(4-(4-cyano-1,5-diphenyl-1H-pyrazol-3-yl)isoxazolo[4,3-d]pyridazin-7-yl)-5-phenyl-1-p-tolyl-1H-pyrazole-4-carbonitrile 
• 1426835-32-6 3-(7-(naphthalen-2-yl)isoxazolo[4,3-d]pyridazin-4-yl)-1,5-diphenyl-1H-pyrazole-4-carbonitrile 
• 1426835-31-5 1,5-diphenyl-3-(7-(thien-2-yl)isoxazolo[4,3-d]pyridazin-4-yl)-1H-pyrazole-4-carbonitrile 
• 1426835-30-4 3-(7-(furan-2-yl)isoxazolo[4,3-d]pyridazin-4-yl)-1,5-diphenyl-1H-pyrazole-4-carbonitrile 
• 1426835-29-1 1,5-diphenyl-3-(7-phenylisoxazolo[4,3-d]pyridazin-4-yl)-1H-pyrazole-4-carbonitrile 
• 1426835-03-1 3-(4-(4-cyano-1,5-diphenyl-1H-pyrazol-3-yl)-2-phenyl-2H-pyrazolo[3,4-d]pyridazin-7-yl)-5-phenyl-1-p-tolyl-1H-pyrazole-4-carbonitrile 
• 1426834-99-2 1,5-diphenyl-3-(2,7-diphenyl-2H-pyrazolo[3,4-d]pyridazin-4-yl)-1H-pyrazole-4-carbonitrile 
• 1261418-38-5 3-(7-methyl-2-phenyl-2H-pyrazolo[3,4-d]pyridazin-4-yl)-1,5-diphenyl-1H-pyrazole-4-carbonitrile 
• 1261418-62-5 C₂₇H₁₇N₇O 
• 1426835-22-4 5-[(3-([4-cyano-1-(4-methylphenyl)-5-phenylpyrazol-3-yl]carbonyl)isoxazol-4-yl)carbonyl]-2,3-diphenylpyrazole-4-carbonitrile 
• 1426835-21-3 3-[3-(naphthalene-2-carbonyl)-isoxazole-4-carbonyl]-1,5-diphenyl-1H-pyrazole-4-carbonitrile 
• 1426835-20-2 1,5-diphenyl-3-[3-(thienyl-2-carbonyl)-isoxazole-4-carbonyl]-1H-pyrazole-4-carbonitrile 
• 1426835-19-9 3-[3-(furan-2-carbonyl)-isoxazole-4-carbonyl]-1,5-diphenyl-1H-pyrazole-4-carbonitrile 
• 1426835-18-8 3-(3-benzoyl-isoxazole-4-carbonyl)-1,5-diphenyl-1H-pyrazole-4-carbonitrile 

Relevant academic research and scientific papers

Synthesis and single-crystal X-ray diffraction analysis of new heterocyclic coloured materials. 3-Arylazo-8H-imidazo[1,2-b] pyrazolo[4,3-d]pyridazines

A simple synthetic strategy is described for the hitherto unreported 3-arylazo-8H-imidazo[1,2-b]pyrazolo[4,3-d]pyridazines 7 is described based on the reaction of 3-acetyl-4-cyano-1,5-diphenylpyrazole hydrazone 3 with the hydrazonoyl halides 1a-l. The structures of such dyes were confirmed by spectroscopic and X-ray crystallographic analyses. The mechanism of formation of such compounds was also discussed.

Polyheterocyclic systems incorporating pyrazole, thiophene, thiazole, and thiadiazole moieties

A variety of polyheterocyclic ring systems having pyrazole, thiophene, thiazole and thiadiazole moieties are synthesized utilizing the reaction of sulfur-functionalized substrates with α-halocarbonyl compounds and hydrazonyl chlorides.