5219-16-9

Basic information

• Product Name: 7-hydroxy-3-(4-methoxyphenyl)-4-methyl-2H-chromen-2-one
• Synonyms: 2H-1-benzopyran-2-one, 7-hydroxy-3-(4-methoxyphenyl)-4-methyl-; 5219-16-9; 7-Hydroxy-3-(4-methoxyphenyl)-4-methylcoumarin
• CAS NO: 5219-16-9
• Molecular Formula: C₁₇H₁₄O₄
• Molecular Weight: 282.2907
• Mol File: 5219-16-9.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 500.6°C at 760 mmHg
• Flash Point: 188.7°C
• Density: 1.284g/cm³
• Vapor Pressure: 1.21E-10mmHg at 25°C
• Refractive Index: 1.623
• CAS DataBase Reference: 7-hydroxy-3-(4-methoxyphenyl)-4-methyl-2H-chromen-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: 7-hydroxy-3-(4-methoxyphenyl)-4-methyl-2H-chromen-2-one(5219-16-9)
• EPA Substance Registry System: 7-hydroxy-3-(4-methoxyphenyl)-4-methyl-2H-chromen-2-one(5219-16-9)

Safety Data

• Hazardous Substances Data: 5219-16-9(Hazardous Substances Data)

Usage

General Description

7-hydroxy-3-(4-methoxyphenyl)-4-methyl-2H-chromen-2-one is a chemical compound that belongs to the class of flavonoids, which are natural compounds found in various fruits, vegetables, and herbs. This specific compound has a complex chemical structure that includes a chromen-2-one backbone with hydroxy, methoxy, and methyl functional groups. It has been found to possess antioxidant, anti-inflammatory, and anti-cancer properties, making it a potential candidate for pharmaceutical and nutraceutical applications. Additionally, it has also shown potential in promoting cardiovascular health and reducing the risk of chronic diseases. The compound's unique structure and beneficial properties make it an interesting target for further research and development.

Upstream product

• 23226-88-2 7-acetoxy-3-(4-methoxy-phenyl)-4-methyl-coumarin 
• 63895-78-3 2-(4-methoxyphenyl)-3-oxobutanenitrile 
• 108-46-3 recorcinol 
• 5219-08-9 2-(4-methoxyphenyl)acetoacetic acid ethyl ester 
• 104-01-8 4-Methoxyphenylacetic acid 
• 89-84-9 2',4'-dihydroxy-4-acetophenone 
• 108-24-7 acetic anhydride 
• 7664-93-9 sulfuric acid 
• 104-47-2 p-methoxybenzylnitrile 
• 81685-26-9 (Z)-3-hydroxy-2-(4-methoxyphenyl)but-2-enenitrile 

Downstream Products

• 5217-88-9 7-methoxy-3-(4-methoxy-phenyl)-4-methyl-coumarin 
• 75256-61-0 7-O-Desyl-3-p-methoxyphenyl-4-methylcoumarin 
• 75256-65-4 2,3-Diphenyl-6-(p-hydroxyphenyl)-5-methyl-7(H)-oxofuro<3,2-g><1>benzopyran 
• 75256-63-2 2,3-Diphenyl-6-p-methoxyphenyl-5-methyl-7(H)-oxofuro<3,2-g><1>benzopyran 
• 75256-70-1 2,3-Diphenyl-6--5-methyl-7(H)-oxofuro<3,2-g><1>benzopyran 
• 75256-74-5 5-Methyl-2,3-diphenyl-6-[4-(2-pyrrolidin-1-yl-ethoxy)-phenyl]-furo[3,2-g]chromen-7-one 
• 75256-71-2 5-Methyl-2,3-diphenyl-6-[4-(3-piperidin-1-yl-propoxy)-phenyl]-furo[3,2-g]chromen-7-one 
• 75256-72-3 5-Methyl-2,3-diphenyl-6-[4-(2-piperazin-1-yl-ethoxy)-phenyl]-furo[3,2-g]chromen-7-one 
• 75256-73-4 5-Methyl-6-[4-(2-morpholin-4-yl-ethoxy)-phenyl]-2,3-diphenyl-furo[3,2-g]chromen-7-one 

Relevant articles and documents

Photocatalytic surface patterning of cellulose using diazonium salts and visible light

Coumarin-functionalized cellulose sheets were chemically modified using a visible light catalyzed "Photo-Meerwein" arylation. Use of a photomask to pattern the surface resulted in directly visible images.

Synthesis of 2,3-Diphenyl-6-(p-substituted phenyl)-5H/methyl-7(H)-oxofurobenzopyrans as Possible Antifertility Agents

Synthesis and antiimplantation activity of some 2,3-diphenyl-6--5H/methyl-7(H)-oxofurobenzopyrans (Va-d and VIa-e) are reported.Of these 2,3-diphenyl-6--5-methyl-7(H)-oxofurobenzopyran (VIa) shows significant activity.