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[2-(4-methoxyphenyl)-4-oxo-4H-chromen-8-yl]acetic acid is a chemical compound belonging to the class of organic compounds known as coumarins and derivatives. It is a derivative of coumarin, a naturally occurring compound found in various plants. This specific compound features a chromen-8-one core with a 4-methoxyphenyl group at the 2-position and an acetic acid group at the 8-position. Its structure suggests potential biological activities and pharmacological properties, such as anti-inflammatory, antioxidant, and anticancer effects, making it a compound of interest for pharmaceutical and medicinal applications.

87627-10-9

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87627-10-9 Usage

Uses

Used in Pharmaceutical Applications:
[2-(4-methoxyphenyl)-4-oxo-4H-chromen-8-yl]acetic acid is used as a pharmaceutical compound for its potential anti-inflammatory, antioxidant, and anticancer effects. [2-(4-methoxyphenyl)-4-oxo-4H-chromen-8-yl]acetic acid's structure and properties make it a promising candidate for the development of new drugs targeting various diseases and conditions.
Used in Medicinal Applications:
In the field of medicine, [2-(4-methoxyphenyl)-4-oxo-4H-chromen-8-yl]acetic acid is used as a therapeutic agent due to its potential to exhibit anti-inflammatory, antioxidant, and anticancer properties. Its pharmacological activities suggest that it could be utilized in the treatment of various illnesses, including those related to inflammation, oxidative stress, and cancer.
Used in Research and Development:
[2-(4-methoxyphenyl)-4-oxo-4H-chromen-8-yl]acetic acid is also used as a research compound in the scientific community. Its unique structure and potential biological activities make it an interesting subject for further study, with the aim of understanding its mechanisms of action and exploring its potential applications in drug discovery and development.
Used in Drug Delivery Systems:
Similar to gallotannin, [2-(4-methoxyphenyl)-4-oxo-4H-chromen-8-yl]acetic acid could be employed in drug delivery systems to enhance its applications and efficacy against specific conditions. Various organic and metallic nanoparticles could be used as carriers for [2-(4-methoxyphenyl)-4-oxo-4H-chromen-8-yl]acetic acid, aiming to improve its delivery, bioavailability, and therapeutic outcomes in targeted treatments.

Check Digit Verification of cas no

The CAS Registry Mumber 87627-10-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,6,2 and 7 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 87627-10:
(7*8)+(6*7)+(5*6)+(4*2)+(3*7)+(2*1)+(1*0)=159
159 % 10 = 9
So 87627-10-9 is a valid CAS Registry Number.

87627-10-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[2-(4-methoxyphenyl)-4-oxochromen-8-yl]acetic acid

1.2 Other means of identification

Product number -
Other names 4H-1-Benzopyran-8-acetic acid,2-(4-methoxyphenyl)-4-oxo

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:87627-10-9 SDS

87627-10-9Relevant academic research and scientific papers

Synthesis and antitumour activity of new derivatives of flavone-8-acetic acid (FAA). Part 2: Ring-substituted derivatives

Aitken, R. Alan,Bibby, Michael C.,Double, John A.,Laws, Andrea L.,Ritchie, Robert B.,Wilson, David W. J.

, p. 215 - 224 (2007/10/03)

A range of 18 derivatives of flavone-8-acetic acid (FAA) with substituents on the 2-phenyl group have been prepared and their anti-tumour activity evaluated in vitro against a panel of human and murine tumour cell lines and in vitro against MAC 15A. There was no clear-cut relationship between in vitro and in vitro activity but the activity in each situation was found to be very sensitive to the precise substitution pattern with closely related isomers giving widely different activities. Some of the compounds, notably l0b,c,j, and r, were active in vitro and these require further studies in order to evaluate their potential for development.

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