150454-83-4 Usage
Uses
Used in Pharmaceutical Industry:
[1,2,4]Triazolo[1,5-a]quinoxalin-4(5H)-one(9CI) is used as a chemical scaffold for the development of novel drugs and biologically active compounds due to its unique structure and potential pharmacological properties.
Used in Antimicrobial Applications:
In the field of antimicrobial research, [1,2,4]Triazolo[1,5-a]quinoxalin-4(5H)-one(9CI) is utilized for its potential to combat various microorganisms, contributing to the development of new antibiotics and antifungal agents.
Used in Anti-inflammatory Applications:
[1,2,4]Triazolo[1,5-a]quinoxalin-4(5H)-one(9CI) is also used as a starting point for the development of anti-inflammatory drugs, targeting the reduction of inflammation and associated symptoms.
Used in Antitumor Applications:
[1,2,4]Triazolo[1,5-a]quinoxalin-4(5H)-one(9CI) is employed in the search for new antineoplastic agents, with the aim of developing treatments for various types of cancer.
Used in Medicinal Chemistry Research:
[1,2,4]Triazolo[1,5-a]quinoxalin-4(5H)-one(9CI) is used as a valuable molecule for further research in the fields of medicinal chemistry, where it can be modified and optimized to enhance its biological activities and therapeutic potential.
Check Digit Verification of cas no
The CAS Registry Mumber 150454-83-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,0,4,5 and 4 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 150454-83:
(8*1)+(7*5)+(6*0)+(5*4)+(4*5)+(3*4)+(2*8)+(1*3)=114
114 % 10 = 4
So 150454-83-4 is a valid CAS Registry Number.
150454-83-4Relevant academic research and scientific papers
Tricyclic Heteroaromatic Systems. 1,2,4-Triazoloquinoxaline
Catarzi, Daniela,Cecchi, Lucia,Colotta, Vittoria,Filacchioni, Guido,Melani, Fabrizio
, p. 1161 - 1163 (2007/10/02)
The parent 1,2,4-triazoloquinoxaline was prepared by a few-step reaction from N1-(2-nitrophenyl)-N3-ethoxalyloxamidrazonate, which afforded the key intermediate diethyl 1-(2-nitrophenyl)-1,2,4-triazole-3,5-dicarboxylate in sat