79815-71-7

Upstream product

• 106367-54-8 3,5-dihydroxy-4-phenylpyrazole 
• 83-13-6 diethyl 2-phenylmalonate 
• 110-91-8 morpholine 
• 79815-55-7 anhydro-1-hydroxy-3-oxo-2,5,7-triphenylpyrazolo<1,2-a>pyrazolium hydroxide 
• 79815-56-8 C₂₁H₁₈N₂O₂ 
• 79815-57-9 anhydro-1-hydroxy-5-methyl-3-oxo-2-phenyl-6,7,8,9-tetrahydropyrazolo<1,2-a>indazolium hydroxide 
• 79815-54-6 anhydro-2,6-diphenyl-1-hydroxy-5-methyl-3-oxopyrazolo<1,2-a>pyrazolium hydroxide 
• 79815-53-5 anhydro-2,5-diphenyl-1-hydroxy-7-methyl-3-oxopyrazolo<1,2-a>pyrazolium hydroxide 
• 76434-58-7 anhydro-5,7-dimethyl-1-hydroxy-3-oxo-2-phenylpyrazolo<1,2-a>pyrazolium hydroxide 
• 79815-52-4 C₁₃H₁₀N₂O₂ 
• 75526-82-8 anhydro-1-hydroxy-3-oxo-2-phenylpyrazolo<1,2-a>pyrazolium hydroxide 

Relevant academic research and scientific papers

2-Phenylmalonpiperadide and 2-phenylmalonmorpholide

The structures of 2-phenylmalonpiperadide (I) and 2-phenylmalonmorpholide (II) was analyzed. The molecular conformations and the packing arrangements of both the compounds were compared. Although chemically similar, the compounds exhibited different molecular conformations. The only conformational similarities were that their respective carbonyl groups were oriented in the same direction and the heterocyclic rings existed in the chair arrangement. The similarities arose due to the same space group and a similar alignment of their phenyl-substituted backbone with respect to the c axis.

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.