58202-26-9

Basic information

• Product Name: 3(2H)-Benzofuranone, 2-(phenylmethyl)-
• CAS NO: 58202-26-9
• Molecular Formula: C15H12O2
• Molecular Weight: 224.259
• Mol File: 58202-26-9.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 3(2H)-Benzofuranone, 2-(phenylmethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 3(2H)-Benzofuranone, 2-(phenylmethyl)-(58202-26-9)
• EPA Substance Registry System: 3(2H)-Benzofuranone, 2-(phenylmethyl)-(58202-26-9)

Safety Data

• Hazardous Substances Data: 58202-26-9(Hazardous Substances Data)

Upstream product

• 37542-14-6 aurone 
• 7169-34-8 3-oxo-2,3-dihydrobenzo[b]furan 
• 100-52-7 benzaldehyde 
• 582-04-7 aurone 
• 4349-62-6 2-benzyloxybenzoyl chloride 
• 14389-86-7 2-benzyloxybenzoic acid 
• 75318-34-2 3-oxo-2-phenylmethylidene-2,3-dihydrobenzo[b]furan 
• 139914-39-9 o-benzyloxy-ω-diazo-acetophenone 

Downstream Products

• 440633-77-2 2-(2-benzylbenzo[b]furan-3-yl)acetonitrile 

Relevant articles and documents

Design, synthesis and biological activities of dihydroaurones

To widen aurones applicability in achromatic food and cosmetic applications, a series of dihydroaurones were designed to mimic natural aurones as well as synthetic aurones. Dihydroaurones have been synthesized from the corresponding aurones by hydrogenation. These dihydroaurones and their corresponding aurones were screened for antioxidant, anti-inflammatory and tyrosinase enzyme inhibitory activity. Synthesized dihydroaurones (3b-f) displayed superior antioxidant activity in superoxide free radical scavenging assay than the standard gallic acid. Dihydroaurones (3b-f) also exhibited significant tyrosinase enzyme inhibitory activity and two dihydroaurones (3h, 3j) showed promising 5-lipoxygenase inhibitory activity.

Synthesis and structure-affinity-activity relationships of novel benzofuran derivatives as MT2 melatonin receptor selective ligands

A series of N-(2-phenylbenzofuran-3-yl) ethyl amide and N-(2-arylalkylbenzofuran-3-yl) ethyl amide derivatives were synthesized and evaluated as melatonin receptor ligands. The affinity of each compound for the two MT1 and MT2 melato

The Stevens -Shift of Oxonium Ylides: A Route to Substituted Tetrahydrofuranones

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