1503-68-0

Basic information

• Product Name: 1-(5-chloro-6-oxo-1-phenyl-1,6-dihydropyridazin-4-yl)triaza-1,2-dien-2-ium
• CAS NO: 1503-68-0
• Molecular Formula: C₁₀H₇ClN₅O
• Molecular Weight: 248.6479
• Mol File: 1503-68-0.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1-(5-chloro-6-oxo-1-phenyl-1,6-dihydropyridazin-4-yl)triaza-1,2-dien-2-ium(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(5-chloro-6-oxo-1-phenyl-1,6-dihydropyridazin-4-yl)triaza-1,2-dien-2-ium(1503-68-0)
• EPA Substance Registry System: 1-(5-chloro-6-oxo-1-phenyl-1,6-dihydropyridazin-4-yl)triaza-1,2-dien-2-ium(1503-68-0)

Safety Data

• Hazardous Substances Data: 1503-68-0(Hazardous Substances Data)

Usage

General Description

1-(5-chloro-6-oxo-1-phenyl-1,6-dihydropyridazin-4-yl) triaza-1,2-dien-2-ium is a chemical compound that belongs to the category of dihydropyridazines. It contains a triaza-dien-ium group and a chloro-oxo-phenyl substituent. Dihydropyridazines are heterocyclic compounds that have potential pharmacological activities and are often used in the development of pharmaceutical drugs. The presence of the chloro and phenyl groups in this compound may contribute to its biological activities and potential as a drug candidate. Further research and investigation are needed to fully understand the properties and potential applications of this chemical compound.

Upstream product

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

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 articles and documents

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

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