215868-47-6 Usage
Uses
Used in Medicinal Chemistry:
6,8-DIFLUORO-4-HEPTADECYL-7-HYDROXYCOUMARIN is used as a potential pharmaceutical compound for its unique structural features, which may contribute to novel therapeutic agents or drug delivery systems. Its fluorinated and alkylated nature could enhance bioavailability, lipophilicity, and target specificity in drug development.
Used in Materials Science:
In the field of materials science, 6,8-DIFLUORO-4-HEPTADECYL-7-HYDROXYCOUMARIN is utilized for its potential to create new materials with specific properties, such as improved stability, reactivity, or selectivity in chemical processes. Its structural attributes may also be leveraged in the development of sensors, catalysts, or other functional materials.
Used in Agrochemicals:
6,8-DIFLUORO-4-HEPTADECYL-7-HYDROXYCOUMARIN is employed in agrochemical research for its potential as a novel active ingredient in pesticides or herbicides. Its unique structure may offer new modes of action or enhanced selectivity and efficacy against pests and weeds, contributing to more sustainable agricultural practices.
Further research and studies are necessary to fully understand the specific properties and potential uses of 6,8-DIFLUORO-4-HEPTADECYL-7-HYDROXYCOUMARIN in these and other fields.
Check Digit Verification of cas no
The CAS Registry Mumber 215868-47-6 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, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 215868-47:
(8*2)+(7*1)+(6*5)+(5*8)+(4*6)+(3*8)+(2*4)+(1*7)=156
156 % 10 = 6
So 215868-47-6 is a valid CAS Registry Number.
InChI:InChI=1/C26H38F2O3/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-20-18-23(29)31-26-21(20)19-22(27)25(30)24(26)28/h18-19,30H,2-17H2,1H3
215868-47-6Relevant 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.
