7483-33-2 Usage
Uses
Used in Pharmaceutical Industry:
2-Quinoxalinecarbonitrile(7CI,8CI,9CI) is used as a potential active pharmaceutical ingredient for its potential biological activities. Due to its quinoxaline structure, it may exhibit properties such as antibacterial, antifungal, antiviral, anti-inflammatory, and anticancer effects, making it a candidate for further research and development in the pharmaceutical field.
Used in Chemical Research:
2-Quinoxalinecarbonitrile(7CI,8CI,9CI) is used as a research compound for understanding its exact properties, characteristics, and potential applications. 2-Quinoxalinecarbonitrile(7CI,8CI,9CI)'s structure and potential reactivity with other molecules make it an interesting subject for chemical research, which could lead to the discovery of new applications and uses in various industries.
Used in Material Science:
2-Quinoxalinecarbonitrile(7CI,8CI,9CI) may be used as a building block or intermediate in the synthesis of more complex molecules with potential applications in material science. Its unique structure and properties could contribute to the development of new materials with specific characteristics, such as improved stability, conductivity, or other desirable properties.
Check Digit Verification of cas no
The CAS Registry Mumber 7483-33-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,8 and 3 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7483-33:
(6*7)+(5*4)+(4*8)+(3*3)+(2*3)+(1*3)=112
112 % 10 = 2
So 7483-33-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H5N3/c10-5-7-6-11-8-3-1-2-4-9(8)12-7/h1-4,6H
7483-33-2Relevant academic research and scientific papers
Oxidative ammonolysis of 2-methylquinoxaline on vanadium-titanium oxide catalyst
Postnikov,Korovina,Kagarlitskii,Krichevskii
, p. 320 - 322 (2008/09/19)
The behavior of 2-methylquinoxaline in the course of oxidative ammonolysis on V-Ti oxide catalyst in a wide range of conditions was studied, and this reaction was examined as a route to 2-quinoxalinecarbonitrile.
AN UNEXPECTED RING-OPENING IN THE REISSERT REACTION ON 2,3-DIPHENYLQUINOXALINE-N-OXIDE.
Nasielski, J.,Heilporn, S.,Nasielski-Hinkens, R.,Tinant, B.,Declercq, J. P.
, p. 7795 - 7804 (2007/10/02)
When quinoxaline-N-oxide 1 is reacted with KCN and benzoyl chloride in water (the Reissert reaction) or methanol, the products are 2-, 5- and 6- chloroquinoxaline (the latter being the major product: 42+/-6percent) and small amounts of 2-cyanoquinoxaline.Using three equivalents of trimethylsilyl cyanide instead of KCN, and dichloromethane as the solvent, leads to a 72percent yield of 2-cyanoquinoxaline.The reaction of trimethylsilyl cyanide and benzoyl chloride with 2,3-diphenylquinoxaline-N-oxide 2 leads to an unexpected ring-opening product 13; its structure is based on spectroscopic data and on an X-ray crystallographic analysis.
