215868-24-9 Usage
Uses
Used in Medicinal Chemistry and Pharmaceuticals:
6,8-Difluoro-7-ethoxy-4-methylcoumarin is used as a therapeutic agent for various diseases due to its antioxidant, anti-inflammatory, and anti-cancer properties. Its potential as a biologically active compound has been studied extensively, highlighting its promise in treating a range of health conditions.
Used in Biochemical and Cellular Studies:
In the field of biochemical and cellular research, 6,8-difluoro-7-ethoxy-4-methylcoumarin serves as a fluorescent probe. It exhibits strong blue fluorescence upon excitation, making it a valuable tool for tracking and visualizing cellular processes and interactions. Its fluorescence properties contribute to its utility in various research applications, enhancing the understanding of biological systems and mechanisms.
Check Digit Verification of cas no
The CAS Registry Mumber 215868-24-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,5,8,6 and 8 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 215868-24:
(8*2)+(7*1)+(6*5)+(5*8)+(4*6)+(3*8)+(2*2)+(1*4)=149
149 % 10 = 9
So 215868-24-9 is a valid CAS Registry Number.
InChI:InChI=1/C12H10F2O3/c1-3-16-12-8(13)5-7-6(2)4-9(15)17-11(7)10(12)14/h4-5H,3H2,1-2H3
215868-24-9Relevant academic research and scientific papers
Derivatives of 6,8-difluoro-7-hydroxycoumarin
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, (2008/06/13)
The present invention comprises 6,8-difluoro-7-hydroxycoumarins and derivatives of 6,8-difluoro-7-hydroxycoumarins, including reactive dyes, dye-conjugates and enzyme substrates. These fluorine-substituted fluorescent dyes typically possess greater photostability and lower pH sensitivity in the physiological pH range than their nonfluorinated analogs, exhibit less fluorescence quenching when conjugated to a substance, possess absorption and emission spectra that closely match those of their nonfluorinated analogs, and also exhibit higher quantum yields than their nonfluorinated analogs.
