87627-20-1 Usage
Uses
Used in Medicinal Chemistry:
(4-oxo-2,3-diphenyl-4H-chromen-8-yl)acetic acid is used as a compound with potential biological activities for anti-inflammatory and antioxidant purposes. Its unique structure and functional groups make it a promising candidate in the field of medicinal chemistry for drug development and pharmaceutical research.
Used in Drug Development:
In the pharmaceutical industry, (4-oxo-2,3-diphenyl-4H-chromen-8-yl)acetic acid is used as a starting material or a structural component in the design and synthesis of new drugs. Its diverse biological activities and structural features allow for the exploration of various therapeutic applications.
Further studies are necessary to fully understand the mechanism of action and potential therapeutic applications of (4-oxo-2,3-diphenyl-4H-chromen-8-yl)acetic acid, which could lead to its use in additional applications across different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 87627-20-1 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, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 87627-20:
(7*8)+(6*7)+(5*6)+(4*2)+(3*7)+(2*2)+(1*0)=161
161 % 10 = 1
So 87627-20-1 is a valid CAS Registry Number.
87627-20-1Relevant academic research and scientific papers
Synthesis and anticancer activities of 3-arylflavone-8-acetic acid derivatives
Yan, Guang-Hua,Li, Xiao-Fang,Ge, Bing-Chen,Shi, Xiu-Dong,Chen, Yu-Fang,Yang, Xue-Mei,Xu, Jiang-Ping,Liu, Shu-Wen,Zhao, Pei-Liang,Zhou, Zhong-Zhen,Zhou, Chun-Qiong,Chen, Wen-Hua
, p. 251 - 257 (2015/01/08)
This paper describes the synthesis and the antiproliferative activities of compounds 9a-r, 3-aryl analogs of flavone-8-acetic acid that bear diverse substituents on the benzene rings at the 2- and 3-positions of the flavone nucleus. Their direct and indir
