19775-47-4 Usage
Chemical class
Dibenzoquinoline alkaloids
1,2,3,9,10-pentamethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline belongs to a class of alkaloids that are derived from the dibenzoquinoline ring system.
Natural occurrence
Plant species
It is a naturally occurring compound found in certain plant species.
Pharmaceutical properties
Potential medicinal applications
The compound is known for its potential pharmaceutical properties, making it an interesting target for further research and development in the field of medicine and pharmacology.
Structure
Unique with five methoxy groups and a methyl group
The compound has a unique structure, featuring five methoxy groups and a methyl group attached to a tetrahydrodibenzquinoline ring system.
Biological activities
Antiproliferative and antitumor effects
It has been studied for its potential biological activities, including antiproliferative (inhibiting cell growth) and antitumor effects.
Research focus
Further investigation into medicinal properties
Due to its complex structure and potential medicinal properties, the compound is a subject of interest for additional research in the fields of medicine and pharmacology.
Check Digit Verification of cas no
The CAS Registry Mumber 19775-47-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,7,7 and 5 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 19775-47:
(7*1)+(6*9)+(5*7)+(4*7)+(3*5)+(2*4)+(1*7)=154
154 % 10 = 4
So 19775-47-4 is a valid CAS Registry Number.
19775-47-4Relevant academic research and scientific papers
Structure Elucidation and Carbon-13 NMR of the New Aporphine Alkaloid 3-Hydroxyglaucine
Roensch, Hasso,Preiss, Alfred,Schreiber, Klaus,Cordoba, Hilda Fernandez de
, p. 744 - 752 (2007/10/02)
From the Lauraceae Ocotea bucherii has been isolated the 3-hydroxy-1,2,9,10-tetramethoxyaporphine (1, 3-hydroxyglaucine) whose structure was determined using spectroscopic methods.Application of various techniques in 13 C NMR led to the spectral assignment of each skeletal carbon in 6>DMSO as well as 6>DMSO/NaOD.- The phenolate anion corresponding to 1 gave rise to pronounced, but opposite variations of the chemical shifts of the ipso and ortho carbons on the one hand or the para carbon on the other.This method proved to be decisive in confirming C-3 as thecarbon bearing the hydroxy group, whereas the alternative C-2 was excluded.
