64360-25-4

Upstream product

• 4173-74-4 1-Phenyl-3-methyl-4-acetyl-5-pyrazolon 
• 93-89-0 benzoic acid ethyl ester 
• 139396-12-6 1-(3-Methyl-5-oxo-1-phenyl-4,5-dihydro-1H-pyrazol-4-yl)-3-phenyl-propane-1,3-dione 
• 210099-61-9 5-methyl-2-phenyl-4-<(E)-3-phenyl-2-propenoyl>-1,2-dihydro-3H-pyrazol-3-one 
• 87100-77-4 1-(5-Hydroxy-3-methyl-1-phenyl-1H-pyrazol-4-yl)-3-phenyl-propane-1,3-dione 
• 7299-58-3 phenylpropiolyl chloride 
• 89-25-8 edaravone 
• 637-44-5 phenylpropyolic acid 
• 37703-59-6 1-phenyl-3-methyl-4-acetylpyrazol-5-one 
• 102-92-1 Cinnamoyl chloride 
• 942-32-5 5-methyl-2-phenyl-2H-pyrazol-3-ol 
• 17313-50-7 3-acetyl-4-hydroxy-6-phenyl-2H-pyran-2-one 
• 87100-59-2 4-Hydroxy-6-phenyl-3-[1-(phenyl-hydrazono)-ethyl]-pyran-2-one 
• 100-63-0 phenylhydrazine 

Relevant academic research and scientific papers

A simple synthesis of 6-phenylpyrano[2,3-c]pyrazol-4(1H)-ones

A novel synthesis of substituted 6-phenylpyrano[2,3-c]pyrazol-4(1H)-ones via reaction of various 2-substituted or 2,5-disubstituted 2,4-dihydro-3H- pyrazol-3-ones with phenylpropynoyl chloride using calcium hydroxide in refluxing 1,4-dioxane is described.

Pyranopyrazoles III synthesis of 1H-pyrano[2,3-c]pyrazol-4-ones [1]

Various derivatives of title ring system were synthesized by Claisen condensation of 4 acetyl-5-hydroxypyrazoles with appropriate esters, followed by acid-catalyzed ring closure.

Synthesis and A1 and A(2A) adenosine binding activity of some pyrano[2,3-c]pyrazol-4-ones

A series of pyrano[2,3-c]pyrazol-4-ones was synthesized and evaluated for bovine brain adenosine A1 and A(2A) receptor binding affinity. Substituents at positions 5 and/or 6 were varied in order to define the structure-activity relationships in

Synthesis of 4-(Acylacetyl)-1-phenyl-2-pyrazolin-5-ones from 3-Acyl-2H-pyran-2,4(3H)-diones. Their Synthetic Applications to Functionalized 4-Oxopyranopyrazole Derivatives.

The phenylhydrazones of 3-acyl-2H-pyran-2,4(3H)-diones (2), in refluxing acetic acid, underwent rearrangement to 4-(acylacetyl)-1-phenyl-2-pyrazolin-5-ones (6), from which some functionalized 4-oxopyranopyrazole derivatives were synthesized.This fi