114967-61-2

Basic information

• Product Name: 3H-Pyrazol-3-one, 2,4-dihydro-5-(2-hydroxyphenyl)-2-phenyl-
• CAS NO: 114967-61-2
• Molecular Formula: C15H12N2O2
• Molecular Weight: 252.272
• Mol File: 114967-61-2.mol

Chemical Properties

• CAS DataBase Reference: 3H-Pyrazol-3-one, 2,4-dihydro-5-(2-hydroxyphenyl)-2-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 3H-Pyrazol-3-one, 2,4-dihydro-5-(2-hydroxyphenyl)-2-phenyl-(114967-61-2)
• EPA Substance Registry System: 3H-Pyrazol-3-one, 2,4-dihydro-5-(2-hydroxyphenyl)-2-phenyl-(114967-61-2)

Safety Data

• Hazardous Substances Data: 114967-61-2(Hazardous Substances Data)

Upstream product

• 114953-95-6 5-(2-Benzyloxy-phenyl)-2-phenyl-2,4-dihydro-pyrazol-3-one 
• 100-63-0 phenylhydrazine 
• 1076-38-6 4-hydroxy[1]benzopyran-2-one 
• 59-88-1 phenylhydrazine hydrochloride 
• 39208-08-7 ethyl 3-<2-(benzyloxy)phenyl>-3-oxopropanoate 

Downstream Products

• 1373432-06-4 (Z)-4-((4-chlorophenyl)hydrazino)-3-(2-hydroxyphenyl)-1-phenyl-2-pyrazolin-5-one 
• 1373432-05-3 (Z)-4-((4-methoxyphenyl)hydrazino)-3-(2-hydroxyphenyl)-1-phenyl-2-pyrazolin-5-one 
• 5186-55-0 (Z)-4-(2-phenylhydrazino)-3-(2-hydroxyphenyl)-1-phenyl-2-pyrazolin-5-one 
• 1373432-07-5 (Z)-4-((4-bromophenyl)hydrazino)-3-(2-hydroxyphenyl)-1-phenyl-2-pyrazolin-5-one 
• 114954-06-2 1-phenyl-3-(2-hydroxyphenyl)-4-formylpyrazole-5-one 
• 107089-95-2 2-phenyl-4-methyl<1>benzopyrano<4,3-c>pyrazol-3(2H)-one 
• 68723-74-0 2-phenyl-2H-chromeno[4,3-c]pyrazol-3-one 
• 114953-98-9 5-(2-Hydroxy-phenyl)-2-phenyl-4-[1-phenylamino-meth-(E)-ylidene]-2,4-dihydro-pyrazol-3-one 
• 114954-00-6 Acetic acid 5-(2-acetoxy-phenyl)-2-phenyl-2H-pyrazol-3-yl ester 

Relevant articles and documents

Synthesis, tautomeric structure, dyeing characteristics, and antimicrobial activity of Novel 4-(2-arylazophenyl)-3-(2-hydroxyphenyl)-1-phenyl-2-pyrazolin- 5-ones

Novel azopyrazolin-5-one dyes 4a-f were synthesized by the regioselective reaction of phenylhydrazine with 2,3,4-chromantrione-3-arylhydrazones 2a-f. The acid dissociation constants pKa for the series prepared were determined and correlated by the Hammett equation. The results of such correlation together with the spectral data indicated that the studied compounds exist predominantly in the hydrazone keto structure, (D) as the Z-configuration. The dyes were applied to polyester fabrics, affording orange-yellow shades and assessments of their dyeing performance are considered. Further, the compounds 4a-f were screened for their antimicrobial activity against various microorganisms.

Tricyclic heteroaromatic systems: Synthesis, [3H]flunitrazepam brain membrane binding inhibition, and structure-activity relationships of 2,3-dihydro-2-aryl-4-R-[1]benzopyrano[4,3-c]pyrazole-3-ones

We report the synthesis and binding activity to the central benzodiazepine receptors of some 2,3-dihydro-2-ary-4-R-[1]benzopyrano[4,3-c]pyrazole-3-ones, which are isosteres of the CGS series. Although the compounds of the CGS series are potent ligands of

THE CORRECT SYNTHESIS OF 2,3-DIHYDRO-2-ARYL-4-R-BENZOPYRANOPYRAZOLE-3-ONES.

The correct synthesis of the title compounds 1a-b and 2a-b is described.The claimed synthesis of 2a from 2-methyl-3-chromonecarbonitrile is shown not to lead to 2a, as previously reported but to 1,4-dihydro-1-phenyl-3-methylbenzopyranopyrazole-4