34647-65-9 Usage
Uses
Used in Pharmaceutical Industry:
6-Methyl-1,2,9,10-tetramethoxy-4H-dibenzo[de,g]quinoline-4,5(6H)-dione is used as a pharmaceutical compound for its potential therapeutic applications. 6-Methyl-1,2,9,10-tetramethoxy-4H-dibenzo[de,g]quinoline-4,5(6H)-dione's unique structure and spectral properties suggest that it may have various biological activities, making it a promising candidate for the development of new drugs.
Used in Chemical Research:
In the field of chemical research, 6-Methyl-1,2,9,10-tetramethoxy-4H-dibenzo[de,g]quinoline-4,5(6H)-dione serves as a valuable compound for studying the properties and reactivity of alkaloids, as well as their potential applications in various chemical processes.
Used in Material Science:
The unique spectral properties and structural features of 6-Methyl-1,2,9,10-tetramethoxy-4H-dibenzo[de,g]quinoline-4,5(6H)-dione make it a candidate for potential applications in material science, such as the development of new materials with specific optical, electronic, or mechanical properties.
Used in Analytical Chemistry:
6-Methyl-1,2,9,10-tetramethoxy-4H-dibenzo[de,g]quinoline-4,5(6H)-dione's distinct absorption maxima in the ultraviolet spectrum make it a useful reference material for analytical chemistry, particularly in the development and calibration of spectroscopic instruments and methods.
Used in Environmental Science:
6-Methyl-1,2,9,10-tetramethoxy-4H-dibenzo[de,g]quinoline-4,5(6H)-dione may also find applications in environmental science, where its unique properties could be utilized for the detection, monitoring, or remediation of environmental contaminants.
Used in Forensic Science:
6-Methyl-1,2,9,10-tetramethoxy-4H-dibenzo[de,g]quinoline-4,5(6H)-dione's distinctive spectral characteristics can be employed in forensic science for the identification and analysis of trace evidence, potentially aiding in the investigation of criminal cases.
References
Ribas, Sueiras, Castedo., Tetrahedron Lett., 3093 (1971)
Check Digit Verification of cas no
The CAS Registry Mumber 34647-65-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,6,4 and 7 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 34647-65:
(7*3)+(6*4)+(5*6)+(4*4)+(3*7)+(2*6)+(1*5)=129
129 % 10 = 9
So 34647-65-9 is a valid CAS Registry Number.
34647-65-9Relevant academic research and scientific papers
FREMY'S SALT OXIDATION OF SOME ISOQUINOLINE ALKALOIDS. BIOGENETIC CONSIDERATIONS
Castedo, Luis,Puga, Alberto,Saa, Jose M.,Suau, Rafael
, p. 2233 - 2236 (2007/10/02)
Fremy's salt oxidation of benzylisoquinoline and aporphine alkaloids to isoquinolones and oxoaporphines is described.Aminium radicals are suggested to account for the observed results.Their possible involvement in alkaloid biosynthesis is considered.
SOURCE OF SOME MINOR ALKALOIDS IN GLAUCIUM FLAVUM
Chervenkova, Violeta B.,Mollov, Nikola M.,Paszyc, Stefan
, p. 2285 - 2288 (2007/10/02)
Air oxidation of glaucine leads to 7,6'-dehydroglaucine and 1,2,9,10-tetramethoxyoxoaporphine, and UV irradiation gives dihydropontevedrine, pontevedrine, glaucine-N-oxide and corunine.These results support the view that glaucine, the main alkaloid in Glaucium flavum, may produce all the more oxidized minor alkaloids present in the plant.Key Word Index-Glaucium flavum; Papaveraceae; alkaloids; glaucine; air oxidation; UV irradiation; dihydropontevedrine.
