71630-83-6 Usage
Description
[1,2,5]Oxadiazolo[3,4-f]quinoxaline (9CI) is a heterocyclic compound with the molecular formula C12H6N4O. It belongs to the class of organic compounds known as quinoxalines and is characterized by its nitrogen-rich structure, containing two nitrogen atoms and two oxygen atoms. This unique chemical has potential applications in various fields due to its distinctive properties and structural features.
Uses
Used in Pharmaceutical Synthesis:
[1,2,5]Oxadiazolo[3,4-f]quinoxaline (9CI) is used as a building block in the synthesis of pharmaceuticals for its potential to contribute to the development of new drugs with enhanced efficacy and selectivity. Its unique structure allows for the creation of diverse bioactive compounds that can target specific biological pathways.
Used in Agrochemical Synthesis:
In the agrochemical industry, [1,2,5]Oxadiazolo[3,4-f]quinoxaline (9CI) is used as a building block for the synthesis of various agrochemicals, such as pesticides and herbicides. Its incorporation into these compounds can lead to improved performance and selectivity, ultimately benefiting agricultural productivity and crop protection.
Used in Optoelectronic and Electronic Materials:
[1,2,5]Oxadiazolo[3,4-f]quinoxaline (9CI) is also utilized in the manufacture of optoelectronic and electronic materials, thanks to its unique properties that make it suitable for various industrial applications. Its use in these materials can contribute to the development of advanced technologies and improve the performance of electronic devices.
Check Digit Verification of cas no
The CAS Registry Mumber 71630-83-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,6,3 and 0 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 71630-83:
(7*7)+(6*1)+(5*6)+(4*3)+(3*0)+(2*8)+(1*3)=116
116 % 10 = 6
So 71630-83-6 is a valid CAS Registry Number.
71630-83-6Relevant articles and documents
Furazan ring opening upon treatment of benzofurazan with ethanolamine to yield quinoxalines
Samsonov
experimental part, p. 2510 - 2512 (2009/02/05)
Heating of benzofurazans with ethanolamine in the presence of catalytic amount of p-toluenesulfonic acid leads to quinoxalines.