82157-89-9 Usage
Uses
Used in Pharmaceutical Industry:
1-(2-methyl-1-phenyl-1H-pyrrolo[3,2-c]cinnolin-3-yl)ethanone is used as a potential pharmaceutical compound for its unique molecular structure. The presence of the pyrrolo[3,2-c]cinnoline ring system, along with the methyl and phenyl groups, may contribute to its potential therapeutic effects. Further research is required to explore its specific applications in drug development.
Used in Chemical Research:
1-(2-methyl-1-phenyl-1H-pyrrolo[3,2-c]cinnolin-3-yl)ethanone is used as a subject of study in chemical research for its complex molecular structure. 1-(2-methyl-1-phenyl-1H-pyrrolo[3,2-c]cinnolin-3-yl)ethanone's unique features may provide insights into new chemical reactions, synthesis methods, or potential applications in various fields, including materials science and drug discovery.
Used in Industrial Applications:
1-(2-methyl-1-phenyl-1H-pyrrolo[3,2-c]cinnolin-3-yl)ethanone may be utilized in industrial applications due to its unique structure. 1-(2-methyl-1-phenyl-1H-pyrrolo[3,2-c]cinnolin-3-yl)ethanone's properties, once fully understood, could be harnessed for specific uses in material development, chemical processes, or other industrial sectors. Further investigation is needed to determine its suitability and potential benefits in these areas.
Check Digit Verification of cas no
The CAS Registry Mumber 82157-89-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,1,5 and 7 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 82157-89:
(7*8)+(6*2)+(5*1)+(4*5)+(3*7)+(2*8)+(1*9)=139
139 % 10 = 9
So 82157-89-9 is a valid CAS Registry Number.
82157-89-9Relevant academic research and scientific papers
Polycondensed Nitrogen Heterocycles. Part 23. Pyrrolocinnolines by a Japp-Klingemann Type Reaction
Cirrincione, Girolamo,Almerico, Anna Maria,Aiello, Enrico,Dattolo, Gaetano
, p. 983 - 985 (2007/10/02)
Pyrrolocinnoline derivatives were obtained by an unusual Japp-Klingemann reaction involving an intramolecular azadehalogenation on the pyrrole nucleus.Such an azadehalogenation represents the first example of Japp-Klingemann reaction in which the e
POLYCONDENSED NITROGEN HETEROCYCLES. PART XI. 1,3-DISUBSTITUTED 2-METHYLPYRROLOCINNOLINE AND 2-ACETYL-3-METHYLPYRROLOBENZOTRIAZINE
Dattolo, Gaetano,Cirrincione, Girolamo,Almerico, Anna Maria,D'Asdia, Isabella,Aiello, Enrico
, p. 681 - 686 (2007/10/02)
The diazotization of 1,3-disubstituted 2-methyl-5-(2-aminophenyl)pyrroles (2) and the intramolecular coupling reaction of the resulting diazonium salts lead to pyrrolobenzotriazine 4 when R = H.Compound 3d inhibited the germination of seeds
