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[2-(3,4-dimethoxyphenyl)-4-oxo-4H-chromen-8-yl]acetic acid is a complex chemical compound that belongs to the class of chromone derivatives. It features a chromen ring system and an acetic acid group, which are characteristic of flavone, a type of natural phenolic compound found in various plants. [2-(3,4-dimethoxyphenyl)-4-oxo-4H-chromen-8-yl]acetic acid's structural features suggest potential pharmacological activities and possible therapeutic applications. The presence of the acetic acid group also indicates its potential for chemical modification and derivatization to create novel compounds with improved properties.

87626-98-0

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87626-98-0 Usage

Uses

Used in Pharmaceutical Applications:
[2-(3,4-dimethoxyphenyl)-4-oxo-4H-chromen-8-yl]acetic acid is used as a pharmaceutical compound for its potential pharmacological activities. Its structural features, including the chromen ring system and the acetic acid group, suggest that it may have therapeutic applications in various areas of medicine.
Used in Chemical Modification and Derivatization:
[2-(3,4-dimethoxyphenyl)-4-oxo-4H-chromen-8-yl]acetic acid is used as a starting material for chemical modification and derivatization. The presence of the acetic acid group allows for the creation of novel compounds with potentially improved properties, which could be beneficial in various industries, including pharmaceuticals, agrochemicals, and materials science.
Used in Research and Development:
[2-(3,4-dimethoxyphenyl)-4-oxo-4H-chromen-8-yl]acetic acid is used as a research compound for further studies and exploration of its potential uses and properties. [2-(3,4-dimethoxyphenyl)-4-oxo-4H-chromen-8-yl]acetic acid's unique structure and potential pharmacological activities make it an interesting candidate for research in various scientific fields.
Used in Drug Delivery Systems:
In the pharmaceutical industry, [2-(3,4-dimethoxyphenyl)-4-oxo-4H-chromen-8-yl]acetic acid could be used as a component in drug delivery systems. Its structural features may allow for the development of novel drug delivery platforms, potentially improving the bioavailability and therapeutic outcomes of various medications.

Check Digit Verification of cas no

The CAS Registry Mumber 87626-98-0 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 6 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 87626-98:
(7*8)+(6*7)+(5*6)+(4*2)+(3*6)+(2*9)+(1*8)=180
180 % 10 = 0
So 87626-98-0 is a valid CAS Registry Number.

87626-98-0SDS

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-(3,4-dimethoxyphenyl)-4-oxochromen-8-yl]acetic acid

1.2 Other means of identification

Product number -
Other names 2-[2-(3,4-dimethoxyphenyl)-4-oxo-chromen-8-yl]acetic acid

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:87626-98-0 SDS

87626-98-0Downstream Products

87626-98-0Relevant 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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