125455-90-5 Usage
General Description
2,3,8,9-tetramethoxy-6,11-dimethyl-6,11-dihydro-5H-indeno[1,2-c]isoquinolin-5-one is a chemical compound with a complex structure. It contains four methoxy groups and two methyl groups attached to a central indeno[1,2-c]isoquinolin-5-one ring system. 2,3,8,9-tetramethoxy-6,11-dimethyl-6,11-dihydro-5H-indeno[1,2-c]isoquinolin-5-one belongs to the class of isoquinoline alkaloids and is known for its potential biological activities. The compound has been studied for its potential pharmacological properties, including anti-inflammatory, antioxidant, and anticancer effects. Due to its unique structure and potential medicinal properties, 2,3,8,9-tetramethoxy-6,11-dimethyl-6,11-dihydro-5H-indeno[1,2-c]isoquinolin-5-one is of interest to researchers in the fields of medicinal chemistry and pharmacology.
Check Digit Verification of cas no
The CAS Registry Mumber 125455-90-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,4,5 and 5 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 125455-90:
(8*1)+(7*2)+(6*5)+(5*4)+(4*5)+(3*5)+(2*9)+(1*0)=125
125 % 10 = 5
So 125455-90-5 is a valid CAS Registry Number.
125455-90-5Relevant articles and documents
BENZOPHENANTHRIDINES. IX. SYNTHESIS OF 11-METHYL-C-NORFAGARONINE METHYL ETHER CHLORIDE FROM (+/-)-13α-HYDROXYXYLOPININE
Sazanova, N. M.,Sladkov, V. I.,Suvorov, N. N.
, p. 1167 - 1169 (2007/10/02)
The previously unknown chloride of 11-methyl-C-norfagaronine methyl ether was synthesized from (+/-)-13α-hydroxyxylopinine in four stages.A reduction in the number of stages in the biometic synthesis of the analog of benzophenanthridine alkaloids was achieved by the Hofmann degradation of α-N-methyl-(+/-)-13α-hydroxyxylopinine p-toluenesulfonate, accompanied by dehydration and oxidation.