19726-12-6

Basic information

• Product Name: Phenol, 2-(5-phenyl-1H-pyrazol-3-yl)-
• CAS NO: 19726-12-6
• Molecular Formula: C15H12N2O
• Molecular Weight: 236.273
• Mol File: 19726-12-6.mol
• Article Data: 14

Chemical Properties

• CAS DataBase Reference: Phenol, 2-(5-phenyl-1H-pyrazol-3-yl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Phenol, 2-(5-phenyl-1H-pyrazol-3-yl)-(19726-12-6)
• EPA Substance Registry System: Phenol, 2-(5-phenyl-1H-pyrazol-3-yl)-(19726-12-6)

Safety Data

• Hazardous Substances Data: 19726-12-6(Hazardous Substances Data)

Upstream product

• 39729-11-8 2'-hydroxychalcone dibromides 
• 4010-33-7 2-acetylphenyl benzoate 
• 39103-33-8 3-hydroxy-1-(2-hydroxyphenyl)-3-phenylprop-2-en-1-one 
• 525-82-6 FLAVONE 
• 1469-94-9 1-(2-hydroxyphenyl)-3-phenyl-1,3-propanedione 
• 49615-93-2 (3-aminobenzo[b]furan-2-yl)phenylmethanone 
• 107095-39-6 2-(3-phenyl-4,5-dihydro-1H-pyrazol-5-yl)phenol 
• 94511-13-4 2-benzoyl-3-p-toluenesulfonylamidobenzofuran 
• 98-88-4 benzoyl chloride 
• 118-93-4 o-hydroxyacetophenone 
• 100-52-7 benzaldehyde 
• 888-12-0 (E)-2'-hydroxy-chalcone 
• 644-78-0 2-hydroxychalcone 
• 1214-47-7 1-(2-hydroxyphenyl)-3-phenylprop-2-en-1-one 

Downstream Products

• 95855-09-7 2-Phenyl-5-oxa-3,3a-diaza-cyclopenta[a]naphthalen-4-one 
• 1394369-72-2 [(manganese(III)(3-(2-hydroxyphenyl)-5-phenyl-pyrazole(-2H))(3-(2-hydroxyphenyl)-5-phenyl-pyrazole(-H))(methanol)2)2(sodium)(formate)] 
• 1394369-76-6 [manganes(III)(3-(2-hydroxyphenyl)-5-phenyl-pyrazole(-H))2(azide)] 

Relevant articles and documents

Synthesis, structure and acetylcholinesterase inhibition activity of new diarylpyrazoles

A variety of diarylpyrazole derivatives III-VI were synthesized and structurally characterized using FTIR, 1H and 13C NMR spectroscopy, and in case of compound VIb by X-ray single crystal analysis. The in vitro biological studies rev

Aurones and Analogues: Promising Heterocyclic Scaffolds for Development of Antioxidant and Antimicrobial Agents

Synthesis of some new multi-functional analogues of 2′-hydroxy chalcone containing isoxazole and pyrazole functions were synthesized, and their pharmacological activity was tested. Chalcone derivatives were synthesized by the reaction of 2′-hydroxy acetophenone with various substituted benzaldehydes in a basic medium. Aurones were isolated upon treatment with mercuric acetate. Synthesized chalcones and aurones were converted into the corresponding isoxazole and pyrazole derivatives upon their reaction with hydroxylamine hydrochloride or hydrazine hydrate, respectively. Structures of the compounds were confirmed by spectroscopic methods. All synthesized compounds were tested for antioxidant and antibacterial potential. Some of those demonstrated excellent antioxidant activity, and one product was identified as a promising antimicrobial candidate.

ESIPT-active organic compounds with white luminescence based on crystallization-induced keto emission (CIKE)

Structurally simple pyrazole derivatives that exhibit excited-state intramolecular proton transfer (ESIPT) were synthesized. While these compounds displayed deep violet fluorescence in solution, in the crystalline state they showed white emission from the