77411-92-8 Usage
Uses
Used in Pharmaceutical Industry:
1-(2-methyl-1-phenyl-1,4-dihydropyrrolo[3,2-b]indol-3-yl)ethanone is used as a potential therapeutic agent for various medical conditions due to its structural resemblance to known bioactive molecules. Its application in this industry is based on the hypothesis that it may exhibit pharmacological effects similar to those of related compounds, which could be beneficial in treating specific diseases or conditions.
Used in Chemical Research:
In the field of chemical research, 1-(2-methyl-1-phenyl-1,4-dihydropyrrolo[3,2-b]indol-3-yl)ethanone serves as a subject for further investigation to understand its chemical properties, reactivity, and potential for synthesis of new compounds. Its complex structure and the presence of a pyrroloindole core make it an interesting candidate for exploring novel chemical reactions and mechanisms.
Check Digit Verification of cas no
The CAS Registry Mumber 77411-92-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,4,1 and 1 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 77411-92:
(7*7)+(6*7)+(5*4)+(4*1)+(3*1)+(2*9)+(1*2)=138
138 % 10 = 8
So 77411-92-8 is a valid CAS Registry Number.
77411-92-8Relevant academic research and scientific papers
Polycondensed Nitrogen Heterocycles. Part 13 . Pyrroloindole by Intramolecular Nucleophilic Substitution Reaction in the Pyrrole Series
Aiello, E.,Dattolo, G.,Cirrincione, G.,Almerico, A. M.
, p. 721 - 724 (2007/10/02)
An intramolecular nucleophilic substitution in the pyrrole series has been generalized.The behaviour of nitro, chlorine, bromine and iodine as leaving groups towards the nucleophilic amino group was observed.An acid catalyzed mechanism has been proposed.
Polycondensed Nitrogen Heterocycles. Part 8. Pyrroloindole
Aiello, Enrico,Dattolo, Gaetano,Cirrincione, Girolamo
, p. 1 - 3 (2007/10/02)
The reduction of the nitro-derivatives (4a-c) with iron-acetic acid leads to the pyrroloindoles (7a-c).This unusual indolization, in which displacement of the heterocycle amino-group occurs, is regarded as a nucleophilic attack by the 2-aminophenyl
