54785-44-3 Usage
Molecular structure
A complex and specific arrangement of atoms, featuring two methoxy groups and a methyl group attached to a benzodioxole ring system.
Classification
Belongs to the class of benzophenanthridine alkaloids, which are naturally occurring compounds found in various plants.
Biological activity
The compound's structure and features contribute to its potential biological activity, making it a subject of interest for further research.
Medicinal properties
Research suggests that 2,3-dimethoxy-13-methyl[1,3]benzodioxolo[5,6-c]phenanthridine may possess antimicrobial, antifungal, and anticancer properties.
Pharmaceutical development
Due to its potential medicinal properties, 2,3-dimethoxy-13-methyl[1,3]benzodioxolo[5,6-c]phenanthridine is considered for possible pharmaceutical development and application in the treatment of various diseases and conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 54785-44-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,7,8 and 5 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 54785-44:
(7*5)+(6*4)+(5*7)+(4*8)+(3*5)+(2*4)+(1*4)=153
153 % 10 = 3
So 54785-44-3 is a valid CAS Registry Number.
54785-44-3Relevant academic research and scientific papers
A formal new access to the benzo[c]phenanthridine alkaloids, synthesis of Nitidine and O-Methyl Fagaronine analogues
Janin,Bisagni
, p. 10305 - 10316 (2007/10/02)
Previously unreported 2-aryl-1-naphthylamines were obtained in good yields from 2-aryl-1-tetraloneoximes by using the Semmler-Wolf reaction but omitting the acetic anhydride usually present in the reaction mixture. From these amines, through the thermal cyclization of their corresponding ethyl carbamates, a new access to the benzo[c]phenanthridin-6(5H)-ones was found. Preparation of water-soluble Nitidine and O-Methyl Fagaronine analogues bearing an alkylamino side chain on the C-6 position was achieved from these compounds.
