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5219-16-9 Usage


7-hydroxy-3-(4-methoxyphenyl)-4-methyl-2H-chromen-2-one is a flavonoid compound characterized by a chromen-2-one backbone with hydroxy, methoxy, and methyl functional groups. It is naturally found in various fruits, vegetables, and herbs and has been identified for its antioxidant, anti-inflammatory, and anti-cancer properties. 7-hydroxy-3-(4-methoxyphenyl)-4-methyl-2H-chromen-2-one also shows promise in promoting cardiovascular health and reducing the risk of chronic diseases, making it a valuable candidate for pharmaceutical and nutraceutical applications.


Used in Pharmaceutical Applications:
7-hydroxy-3-(4-methoxyphenyl)-4-methyl-2H-chromen-2-one is used as a therapeutic agent for its antioxidant, anti-inflammatory, and anti-cancer properties. It can potentially be developed into a pharmaceutical product to treat various diseases and conditions, including cancer and chronic inflammatory disorders.
Used in Nutraceutical Applications:
In the nutraceutical industry, 7-hydroxy-3-(4-methoxyphenyl)-4-methyl-2H-chromen-2-one is used as a dietary supplement or functional food ingredient to promote overall health and well-being. Its antioxidant and anti-inflammatory properties can contribute to the prevention of chronic diseases and support a healthy immune system.
Used in Cardiovascular Health Applications:
7-hydroxy-3-(4-methoxyphenyl)-4-methyl-2H-chromen-2-one is used as a cardiovascular health promoter due to its potential to improve heart function and reduce the risk of cardiovascular diseases. Its antioxidant properties can help protect the heart from oxidative stress and inflammation, contributing to better cardiovascular health.
Used in Cosmetic Applications:
In the cosmetic industry, 7-hydroxy-3-(4-methoxyphenyl)-4-methyl-2H-chromen-2-one can be used as an active ingredient in skincare products for its antioxidant and anti-inflammatory properties. It may help protect the skin from environmental damage, reduce inflammation, and promote a healthier, more youthful appearance.
Used in Agricultural Applications:
7-hydroxy-3-(4-methoxyphenyl)-4-methyl-2H-chromen-2-one can be used in agriculture as a natural pesticide or growth promoter due to its antioxidant and anti-inflammatory properties. It may help protect plants from oxidative stress and promote healthy growth, reducing the need for synthetic chemicals in agriculture.
Overall, the diverse applications of 7-hydroxy-3-(4-methoxyphenyl)-4-methyl-2H-chromen-2-one highlight its potential as a versatile compound with significant health and wellness benefits. Further research and development are needed to fully explore its potential and optimize its use in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 5219-16-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,1 and 9 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5219-16:
79 % 10 = 9
So 5219-16-9 is a valid CAS Registry Number.



According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017


1.1 GHS Product identifier

Product name 7-hydroxy-3-(4-methoxyphenyl)-4-methylchromen-2-one

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5219-16-9 SDS

5219-16-9Relevant articles and documents

Photocatalytic surface patterning of cellulose using diazonium salts and visible light

Schroll, Peter,Fehl, Charlie,Dankesreiter, Stephan,Koenig, Burkhard

supporting information, p. 6510 - 6514 (2013/09/24)

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

Rao, B. Vittal,Somayajulu, V. V.

, p. 232 - 234 (2007/10/02)

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.

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