76426-56-7

Basic information

• Product Name: 5.7-Dimethyl-2-(p-chlorphenyl)-1-oxo-1H-pyrazol<1.2-a>pyrazol-4-ium-3-olat
• CAS NO: 76426-56-7
• Molecular Weight: 274.707
• Mol File: 76426-56-7.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 5.7-Dimethyl-2-(p-chlorphenyl)-1-oxo-1H-pyrazol<1.2-a>pyrazol-4-ium-3-olat(CAS DataBase Reference)
• NIST Chemistry Reference: 5.7-Dimethyl-2-(p-chlorphenyl)-1-oxo-1H-pyrazol<1.2-a>pyrazol-4-ium-3-olat(76426-56-7)
• EPA Substance Registry System: 5.7-Dimethyl-2-(p-chlorphenyl)-1-oxo-1H-pyrazol<1.2-a>pyrazol-4-ium-3-olat(76426-56-7)

Safety Data

• Hazardous Substances Data: 76426-56-7(Hazardous Substances Data)

Upstream product

• 19677-37-3 diethyl 2-(p-chlorophenyl)malonate 
• 67-51-6 3,5-dimethyl-1H-pyrazole 
• 68823-00-7 (4-chloro-phenyl)-malonyl dichloride 
• 106367-56-0 4-(p-methoxyphenyl)-3,5-dihydroxypyrazole 
• 123-54-6 acetylacetone 

Relevant articles and documents

Studies on Paraionic Compounds. Anhydro-1-hydroxy-3-oxopyrazolopyrazolium Hydroxides. Formation and Stability of a Novel Series of 4n? Heterocyclic Betaines.

Different substituted anhydro-1-hydroxy-3-oxopyrazolopyrazolium hydroxides were prepared by the reaction of 1,3-dicarbonyl compounds with derivatives of 4-phenyl-3,5-dihydroxypyrazole.These diazapentalene derivatives belong to new series of 4n? cyclic betaines which are named "paraionic" heterocycles.The effects of substituents on the stability of both the anionic and the cationic rings were kinetically studied.Selective cleavage of either the anionic or the cationic ring was achieved by varying the conditions of the reaction with morpholine.Electron releasing groups on the cationic ring and electron attracting groups on the anionic ring enhance the stability of the bicyclic system.They also cause a hypsochromic shift of the visible light absorption.