39685-86-4 Usage
Uses
Used in Pharmaceutical Research:
2-Benzofurylglyoxylic acid is utilized as a research compound for its enzyme-inhibiting properties, which can be crucial in the development of new drugs targeting specific biological pathways.
Used in Organic Synthesis:
In the field of organic chemistry, 2-Benzofurylglyoxylic acid is employed as a precursor in the synthesis of other organic compounds, contributing to the creation of novel molecules with potential applications in various industries.
Used in Enzyme Inhibition Studies:
2-Benzofurylglyoxylic acid is used as an enzyme inhibitor in biological and medical research, helping to understand and potentially control the activity of enzymes that may be implicated in diseases or other conditions.
If further applications are identified in specific industries based on additional materials or research, they can be listed as follows:
Used in [Specific Application Industry]:
2-Benzofurylglyoxylic acid is used as [specific application type] for [reason for its application in that industry], highlighting its diverse utility across different scientific and industrial domains.
Check Digit Verification of cas no
The CAS Registry Mumber 39685-86-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,6,8 and 5 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 39685-86:
(7*3)+(6*9)+(5*6)+(4*8)+(3*5)+(2*8)+(1*6)=174
174 % 10 = 4
So 39685-86-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H6O4/c11-9(10(12)13)8-5-6-3-1-2-4-7(6)14-8/h1-5H,(H,12,13)
39685-86-4Relevant academic research and scientific papers
Zheng, Changge,Zhai, Wenji,Hong, Jianquan,Zhang, Xiaoxiao,Zhu, Zhenhua,Wang, Ling
, p. 3008 - 3013 (2017)
Two fluorescent nucleosides were synthesized via incorporating benzothiophene and benzofuran into position 5 of 6-aza-uridines. With more intensive push-pull interactions between electron-deficient uridine core and electron-rich extended aromatic moieties
Reaction of 2-(halogenomethyl)-quinoxalines and -quinoline with hydroxybenzoic acids and their esters
Sarodnick,Hilfert,Kempter,Kleinpeter
, p. 714 - 720 (2007/10/03)
In the presence of a base the title compounds react to products with ether structure (4, 6), or with ester structure (3), or to structure 5 containing both functionalities in dependence on the mole ratio of the starting substances, on reaction conditions
