122379-63-9 Usage
Uses
Used in Pharmaceutical Industry:
4-Methoxy-7-azaindole is used as a key intermediate in the synthesis of various pharmaceuticals and organic compounds. Its unique structure and properties make it a valuable component in the development of new drugs and therapeutic agents.
Used in Medicinal Applications:
4-Methoxy-7-azaindole is used as a potential antiviral and anticancer agent. Its medicinal properties have been studied, and it has shown promise in inhibiting the growth of viruses and cancer cells, offering a new avenue for the treatment of viral infections and cancer.
Used in Organic Light-Emitting Diodes (OLEDs):
4-Methoxy-7-azaindole is used in the development of organic light-emitting diodes and other electronic applications. Its unique electronic properties make it a promising candidate for improving the performance and efficiency of OLEDs and other electronic devices.
Check Digit Verification of cas no
The CAS Registry Mumber 122379-63-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,3,7 and 9 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 122379-63:
(8*1)+(7*2)+(6*2)+(5*3)+(4*7)+(3*9)+(2*6)+(1*3)=119
119 % 10 = 9
So 122379-63-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H8N2O/c1-11-7-3-5-10-8-6(7)2-4-9-8/h2-5H,1H3,(H,9,10)
122379-63-9Relevant academic research and scientific papers
PYRIMIDINE AND TRIAZINE DERIVATIVES AND THEIR USE AS AXL INHIBITORS
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Page/Page column 91, (2016/07/05)
Compounds of the general formula(I): (I) processes for the preparation of these compounds, compositions containing these compounds, and the uses of these compounds.
The Synthesis of 5-Azaindoles by Substitution-Rearrangement of 7-Azaindoles upon Treatment with Certain Primary Amines
Girgis, Nabih S.,Larson, Steven B.,Robins, Roland K.,Cottam, Howard B.
, p. 317 - 325 (2007/10/02)
Certain 4-substituted 1H-pyrrolopyridines (7-azaindoles) undergo a nucleophilic substitution-rearrangement upon treatment with various primary amines at elevated temperatures to yield N-1-substituted 4-amino-1H-pyrrolopyridines (5-azaindoles).Treatment of the same 7-azaindoles with secondary amines under the same reaction conditions led to simple nucleophilic substitution products.