82301-52-8

Basic information

• Product Name: 5(4H)-Oxazolone, 4-[(4-hydroxyphenyl)methylene]-2-phenyl-, (4Z)-
• CAS NO: 82301-52-8
• Molecular Formula: C16H11NO3
• Molecular Weight: 265.268
• Mol File: 82301-52-8.mol
• Article Data: 31

Chemical Properties

• CAS DataBase Reference: 5(4H)-Oxazolone, 4-[(4-hydroxyphenyl)methylene]-2-phenyl-, (4Z)-(CAS DataBase Reference)
• NIST Chemistry Reference: 5(4H)-Oxazolone, 4-[(4-hydroxyphenyl)methylene]-2-phenyl-, (4Z)-(82301-52-8)
• EPA Substance Registry System: 5(4H)-Oxazolone, 4-[(4-hydroxyphenyl)methylene]-2-phenyl-, (4Z)-(82301-52-8)

Safety Data

• Hazardous Substances Data: 82301-52-8(Hazardous Substances Data)

Upstream product

• 32089-82-0 2-benzoylamino-3-(4-hydroxy-phenyl)-acrylic acid 
• 495-69-2 Hippuric Acid 
• 108-24-7 acetic anhydride 
• 123-08-0 4-hydroxy-benzaldehyde 
• 98-88-4 benzoyl chloride 
• 1199-01-5 2-phenylazlactone 
• 6515-21-5 4-methoxymethoxy-benzaldehyde 

Downstream Products

• 64896-32-8 (Z)-2-benzamido-3-(p-hydroxyphenyl)-2-propenic acid 
• 136712-94-2 3-(Benzothiazol-2-ylamino)-5-[1-(4-hydroxy-phenyl)-meth-(Z)-ylidene]-2-phenyl-3,5-dihydro-imidazol-4-one 
• 1304503-92-1 1-[2''-[1',3'-dioxo-1',3'-dihyro-(2'H)-isoindole-2'-ylmethyl]-1'',3'',4''-thiadiazol-5''-yl]-4-(4'''-hydroxybenzylidiene)-4,5-dihydro-2-phenylimidazol-5-one 
• 1276667-51-6 N-[(E)-2-(4-hydroxyphenyl)-1-(6-methyl-1H-benzimidazol-2-yl)vinyl]benzamide 
• 1276667-39-0 N-[(E)-1-(1H-benzimidazol-2-yl)-2-(4-hydroxyphenyl)vinyl]benzamide 
• 1276667-45-8 N-[(E)-2-(4-hydroxyphenyl)-1-(6-nitro-1H-benzimidazol-2-yl)vinyl]benzamide 
• 342382-71-2 N-[1-(1H-benzimidazol-2-yl)-2-(4-hydroxyphenyl)vinyl]benzamide 
• 138973-08-7 1,4-Bis(5'-(4-hydroxybenzylidene)-2'-phenyl-4'-imidazolinone-3'-ylamino)phthalazine 
• 136713-09-2 3-(Benzooxazol-2-ylamino)-5-[1-(4-hydroxy-phenyl)-meth-(Z)-ylidene]-2-phenyl-3,5-dihydro-imidazol-4-one 
• 136713-01-4 3-(1H-Benzoimidazol-2-ylamino)-5-[1-(4-hydroxy-phenyl)-meth-(Z)-ylidene]-2-phenyl-3,5-dihydro-imidazol-4-one 
• 139596-94-4 N-{4-[1-(4-Hydroxy-phenyl)-meth-(Z)-ylidene]-5-oxo-2-phenyl-4,5-dihydro-imidazol-1-yl}-isonicotinamide 

Relevant articles and documents

Design, Synthesis, and Antimicrobial Activity of Novel Fluorine-Containing Imidazolones

Abstract: A simple synthetic protocol have been developed for the preparation of novelN-(4-benzylidene-5-oxo-2-phenyl-4,5-dihydro-1H-imidazol-1-yl)-N′-phenylthiourea derivatives by the reaction of4-benzylidene-2-phenyl-4,5-dihydro-1,3-oxazol-5-ones with N

Sulfanilic acid-catalyzed green synthesis of 4-Arylidene-2-phenyl-5(4H)-Oxazolones

This study is focused on the catalytic activity of sulfanilic acid (SA) in the straightforward synthesis of 4-Arylidene-2-phenyl-5(4H)-oxazolones via condensation of aromatic aldehydes, hippuric acid, and acetic anhydride under green experimental conditio

An ionic liquid gel: A heterogeneous catalyst for Erlenmeyer-Plochl and Henry reactions

An ionic liquid gel has been prepared by entrapping 1-butyl-3-methylimidazolium hydroxide ([Bmim]OH) in an aqueous agar gel. The ionic liquid gel has been characterized by Fourier transform infrared (FT-IR), Fourier transform Raman (FT-Raman) spectroscopy, scanning electron microscopy (SEM), thermogravimetric analysis (TGA) and energy dispersive X-ray analysis (EDX). The ionic liquid gel has been successfully employed as a heterogeneous catalyst in the Erlenmeyer-Plochl reaction involving aldehydes, hippuric acid and acetic anhydride as well as in the Henry reaction between aldehydes and nitromethane in ethanol at room temperature. The heterogeneity of the ionic liquid gel has been confirmed by conducting hot filtration tests and leaching studies. Additionally, the ionic liquid gel could be easily recovered by simple filtration and reused five times without significant loss in catalytic activity.