69737-11-7 Usage
Uses
Used in Pharmaceutical Research:
1-(2-chlorophenyl)-2-(3-phenylquinoxalin-2-yl)ethenamine is used as a research compound for its potential therapeutic effects. 1-(2-chlorophenyl)-2-(3-phenylquinoxalin-2-yl)ethenamine's specific properties and potential hazards would need to be determined through further research and testing.
Used in Chemical Synthesis:
1-(2-chlorophenyl)-2-(3-phenylquinoxalin-2-yl)ethenamine can be used as a building block or intermediate in the synthesis of more complex molecules, particularly in the field of medicinal chemistry. Its unique structure may allow for the development of new drugs with novel mechanisms of action.
Used in Drug Design:
In the field of drug design, 1-(2-chlorophenyl)-2-(3-phenylquinoxalin-2-yl)ethenamine may be used as a starting point for the development of new pharmaceuticals. Its structure can be modified and optimized to target specific biological pathways or receptors, potentially leading to the discovery of new treatments for various diseases.
Check Digit Verification of cas no
The CAS Registry Mumber 69737-11-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,7,3 and 7 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 69737-11:
(7*6)+(6*9)+(5*7)+(4*3)+(3*7)+(2*1)+(1*1)=167
167 % 10 = 7
So 69737-11-7 is a valid CAS Registry Number.
69737-11-7Relevant academic research and scientific papers
Action d'organolithiens sur la methyl-2 quinoxaline. Etude de la reactivite des adduits
Mettey, Yvette,Vierfond, Jean-Michel,Thal, Claude,Miocque, Marcel
, p. 133 - 137 (2007/10/02)
The action of organolithium reagents such as phenyllithium or n-butyllithium on 2-methylquinoxaline gave lithiation of the methyl group which upon reaction with electrophiles produce side chain alkenyl derivatives.On the other hand organolithium reagents react with the quinoxaline azomethine bond to give 1-lithio-2-alkyl(or aryl)-3-methylquinoxalines which can be further lithiated on the methyl group to give 2-alkyl(or aryl)-3-alkenylquinoxaline derivatives.The adducts can be condensed with electrophiles such as benzonitrile or methyl benzoate but only methyl benzoate leads to N condensed derivatives.Furthermore substituted 1,2,3,4-tetraquinoxalines are available via the above lithio intermediates.
