1503-68-0

Usage

Uses

Used in Pharmaceutical Development:
1-(5-chloro-6-oxo-1-phenyl-1,6-dihydropyridazin-4-yl)triaza-1,2-dien-2-ium is used as a potential drug candidate for [application reason] due to its dihydropyridazine structure and the presence of the chloro and phenyl groups, which may enhance its biological activities.
Further research and investigation are required to fully understand the properties and potential applications of this chemical compound in various industries.

Upstream product

• 1698-63-1 5-bromo-4-chloro-2-phenyl-2H-pyridazin-3-one 
• 1698-53-9 4,5-dichloro-1-phenylpyridazin-6-one 
• 40175-80-2 5-azido-4-chloropyridazin-3(2H)-one 
• 71-43-2 benzene 

Downstream Products

• 1588523-07-2 C₁₅H₁₂ClN₅O₃ 
• 1549706-61-7 ethyl 1-(6-oxo-1-phenyl-5-(2-oxa-6-azaspiro[3.3]heptan-6-yl)-1,6-dihydropyridazin-4-yl)-1H-1,2,3-triazole-4-carboxylate 
• 40376-58-7 5-(4-acetyl-5-methyl-1H-1,2,3-triazol-1-yl)-4-chloro-2-phenylpyridazin-3(2H)-one 
• 1353166-68-3 C₂₂H₂₄N₆O₄ 
• 1353166-67-2 C₂₃H₂₄N₆O₄ 
• 1353166-66-1 C₂₀H₂₀N₆O₄ 
• 1353166-65-0 C₁₇H₁₄N₆O₄ 
• 1353166-77-4 C₂₆H₂₅N₇O₄ 
• 1353166-75-2 C₂₂H₂₆N₆O₅ 
• 1353166-70-7 C₂₄H₂₀N₆O₅ 
• 1353166-69-4 C₂₀H₂₀N₆O₆ 

Relevant academic research and scientific papers

Targeting the Warburg Effect in cancer; Relationships for 2-arylpyridazinones as inhibitors of the key glycolytic enzyme 6-phosphofructo-2-kinase/2,6-bisphosphatase 3 (PFKFB3)

High-throughput screening of a small-molecule library identified a 5-triazolo-2-arylpyridazinone as a novel inhibitor of the important glycolytic enzyme 6-phosphofructo-2-kinase/2,6-bisphosphatase 3 (PFKFB3) Such inhibitors are of interest due to PFKFB3's

One-pot synthesis of [1,2,3]triazole-fused pyrazinopyridazindione tricycles by a 'click and activate' approach

Substituted [1,2,3]triazole-fused pyrazinopyridazindione tricycles were synthesized in a four-component, stepwise condensation. The key step in this one-pot process was a thermal [3+2] triazole formation which activated the adjacent position and set the s

A "click and activate" Approach in one-pot synthesis of a triazolyl-pyridazinone library

A "click and activate" strategy was designed and executed in a four-component, stepwise condensation that led to a trisubstituted triazolyl-pyridazinone library. This one-pot process included regioselective azide substitution at 2-substituted-4,5-dichloro

Efficient N-arylation of pyridazin-3(2H)-ones

A variety of substituted pyridazin-3(2H)-ones are directly N-arylated in good yield using lead tetraacetate/zinc chloride in benzene or in substituted benzenes including chloro- and bromobenzene. A variety of substituted pyridazin-3(2H)-ones are directly N-arylated in good yield using lead tetraacetate/zinc chloride in benzene or in substituted benzenes including chloro- and bromobenzene.