4439-68-3 Usage
Uses
Used in Pharmaceutical Industry:
4-Hydroxy-7-(hydroxymethyl)-5H-furo[3,2-g][1]benzopyran-5-one is used as a potential therapeutic agent for various conditions due to its anti-inflammatory, anti-cancer, and anti-oxidative effects. Its pharmacological properties make it a candidate for the development of new drugs to treat inflammation, cancer, and oxidative stress-related disorders.
Used in Cosmetic Industry:
Despite its phototoxic properties, 4-Hydroxy-7-(hydroxymethyl)-5H-furo[3,2-g][1]benzopyran-5-one can be used in cosmetic formulations with proper precautions and formulations to minimize skin irritation and reactions when exposed to sunlight. Its anti-inflammatory and anti-oxidative properties may contribute to the development of skincare products with beneficial effects on the skin.
Used in Research and Development:
4-Hydroxy-7-(hydroxymethyl)-5H-furo[3,2-g][1]benzopyran-5-one serves as a valuable compound for scientific research and development in the field of chemistry, biology, and pharmacology. Its unique structure and properties allow researchers to study its mechanisms of action, potential applications, and ways to mitigate its phototoxic effects.
Check Digit Verification of cas no
The CAS Registry Mumber 4439-68-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,3 and 9 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4439-68:
(6*4)+(5*4)+(4*3)+(3*9)+(2*6)+(1*8)=103
103 % 10 = 3
So 4439-68-3 is a valid CAS Registry Number.
4439-68-3Relevant academic research and scientific papers
Chromones from the tubers of Eranthis cilicica and their antioxidant activity
Kuroda, Minpei,Uchida, Singo,Watanabe, Kazuki,Mimaki, Yoshihiro
experimental part, p. 288 - 293 (2009/09/08)
Chemical studies on the constituents of Eranthis cilicica led to isolation of ten chromone derivatives, two of which were previously known. Comprehensive spectroscopic analysis, including extensive 1D and 2D NMR data, and the results of enzymatic hydrolys