215868-24-9 Usage
General Description
6,8-Difluoro-7-ethoxy-4-methylcoumarin is a chemical compound that belongs to the coumarin family. It is a derivative of coumarin, containing two fluorine atoms at positions 6 and 8, an ethoxy group at position 7, and a methyl group at position 4. 6,8-DIFLUORO-7-ETHOXY-4-METHYLCOUMARIN is commonly used in the field of medicinal chemistry and pharmaceuticals due to its potential biological and pharmacological activities. It has been studied for its antioxidant, anti-inflammatory, and anti-cancer properties, and it shows potential as a therapeutic agent for various diseases. Additionally, it is used as a fluorescent probe in biochemical and cellular studies, as it emits a strong blue fluorescence upon excitation. Therefore, 6,8-difluoro-7-ethoxy-4-methylcoumarin is a versatile compound with promising applications in both research and industry.
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 articles and documents
Derivatives of 6,8-difluoro-7-hydroxycoumarin
-
, (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.
