87626-92-4 Usage
Uses
Used in Pharmaceutical Applications:
[2-(3-methoxyphenyl)-4-oxo-4H-chromen-8-yl]acetic acid is used as a potential pharmaceutical agent for its structural resemblance to coumarin. [2-(3-methoxyphenyl)-4-oxo-4H-chromen-8-yl]acetic acid may exhibit anti-inflammatory, anti-coagulant, and anti-cancer properties, similar to its parent compound, coumarin.
Used in Research and Development:
In the field of scientific research, [2-(3-methoxyphenyl)-4-oxo-4H-chromen-8-yl]acetic acid serves as a valuable compound for further investigation into its potential applications and effects. This may include exploring its use in drug development, understanding its interactions with biological systems, and identifying any possible side effects or limitations.
Used in Chemical Synthesis:
[2-(3-methoxyphenyl)-4-oxo-4H-chromen-8-yl]acetic acid may also be utilized as a key intermediate in the synthesis of other complex organic compounds, particularly those with potential pharmaceutical or chemical applications. Its unique structure and functional groups make it a promising candidate for use in the development of novel molecules with specific properties and functions.
Check Digit Verification of cas no
The CAS Registry Mumber 87626-92-4 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 2 respectively.
Calculate Digit Verification of CAS Registry Number 87626-92:
(7*8)+(6*7)+(5*6)+(4*2)+(3*6)+(2*9)+(1*2)=174
174 % 10 = 4
So 87626-92-4 is a valid CAS Registry Number.
87626-92-4Relevant 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.
