53377-61-0 Usage
General Description
1,3,5-Trihydroxy-4-prenylxanthone is a chemical compound which belongs to the group of xanthones, a class of polyphenolic compounds. Xanthones, and specifically prenylated xanthones such as 1,3,5-Trihydroxy-4-prenylxanthone, are commonly found in many plants and have been heavily researched for their antimicrobial, antimutagenic, anti-inflammatory, and antiviral properties. Among their numerous pharmacological benefits, they are also known to exhibit anti-cancer activities. Despite its potential health benefits, the safe and effective therapeutic dosing of 1,3,5-Trihydroxy-4-prenylxanthone has yet to be fully researched and established.
Check Digit Verification of cas no
The CAS Registry Mumber 53377-61-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,3,7 and 7 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 53377-61:
(7*5)+(6*3)+(5*3)+(4*7)+(3*7)+(2*6)+(1*1)=130
130 % 10 = 0
So 53377-61-0 is a valid CAS Registry Number.
53377-61-0Relevant articles and documents
Synthesis of 2-hydroxy-3-methylbut-3-enyl substituted coumarins and xanthones as natural products. Application of the Schenck ene reaction of singlet oxygen with ortho-prenylphenol precursors
Helesbeux, Jean-Jacques,Duval, Olivier,Dartiguelongue, Caroline,Séraphin, Denis,Oger, Jean-Michel,Richomme, Pascal
, p. 2293 - 2300 (2004)
Application of our original photooxidation-reduction methodology to prenylated dihydroxycoumarin and trihydroxyxanthone compounds led to the corresponding ortho-(2-hydroxy-3-methylbut-3-enyl)phenol derivatives with yields ranging from 8 to 65%. In most of the reported experiments, the oxidation products distribution, after the photooxygenation step, was controlled by the competition between the large group effect and the stabilising phenolic assistance effect. We also showed that ortho-(3-hydroxy-3- methylbut-1-enyl)phenol derivatives could be considered as biogenetic precursors of 2,2-dimethylbenzopyranic structures.
