6639-82-3 Usage
Uses
Used in Pharmaceutical Research:
6-Methoxyquinoxaline is used as a building block in pharmaceutical research for its potential biological activities. Its anti-inflammatory and anti-cancer properties make it a valuable component in the development of new drugs and therapeutic agents.
Used in Organic Synthesis:
In the field of organic synthesis, 6-Methoxyquinoxaline is utilized as a key intermediate for the synthesis of various complex organic molecules. Its unique structure allows for the formation of diverse chemical entities, contributing to the advancement of chemical research and the creation of novel compounds with potential applications.
Used in Drug Development:
6-Methoxyquinoxaline is employed in drug development as a promising candidate for the creation of new therapeutic agents. Its potential biological activities, such as anti-inflammatory and anti-cancer effects, make it an attractive starting point for the design and synthesis of innovative pharmaceuticals aimed at treating various diseases and conditions.
Used in Medicinal Chemistry:
In medicinal chemistry, 6-Methoxyquinoxaline serves as a versatile compound for the exploration of structure-activity relationships and the optimization of drug candidates. Its unique chemical properties and potential biological activities enable researchers to investigate its interactions with biological targets and develop more effective and selective therapeutic agents.
Overall, 6-Methoxyquinoxaline's diverse applications in pharmaceutical research, organic synthesis, drug development, and medicinal chemistry underscore its importance and potential in the field of chemistry and drug discovery.
Check Digit Verification of cas no
The CAS Registry Mumber 6639-82-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,3 and 9 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6639-82:
(6*6)+(5*6)+(4*3)+(3*9)+(2*8)+(1*2)=123
123 % 10 = 3
So 6639-82-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H8N2O/c1-12-7-2-3-8-9(6-7)11-5-4-10-8/h2-6H,1H3
6639-82-3Relevant academic research and scientific papers
Ag-TiO2/clay composite photocatalyst for the oxidation-cyclization of 1,2-diamine compounds with propylene glycol or alcohols
Selvam, Kaliyamoorthy,Annadhasan, Mari,Velmurugan, Rengasamy,Swaminathan, Meenakshisundaram
experimental part, p. 831 - 837 (2010/09/06)
Silver-loaded TiO2 (Ag-TiO2) and acidic clay (K10 montmorillonite) composite photocatalyst has been successfully applied for the light-induced conversion of o-phenylenediamine (OPD) and its derivatives to substituted benzimidazoles with various alcohols in acetonitrile using UV-A and solar light. The influence of the various photocatalysts, solvents, and substituents on the yield and selectivity of the products has been investigated. The mechanism of photocatalysis is proposed. Loading silver on TiO2 enhances product yield and selectivity both in UV and solar light. In the presence of primary alcohols, 2-aminothiophenol forms only disulfide and hence Ag-TiO2/ clay can be used as a green catalyst for the synthesis of disulfides.
The Thermolysis of Polyazapentadienes. Part 2. Formation of Quinoxalines from 5-Aryl-1-phenyl-1,2,5-triazapentadienes
McNab, Hamish
, p. 1941 - 1946 (2007/10/02)
Thermolysis in the gas phase of 5-(p-substituted phenyl)-1-phenyl-1,2,5-triazapentadienes at 600 deg C and 10-2 Torr gives 6-substituted quinoxalines.The yield is ca. 30 percent, and is independent of the electronic nature of the substituent.The corresponding 5-(o-substituted) derivatives give 5-substituted quinoxalines, though the yield is lower, and quinoxaline itself is a major contaminant, due to ipso attack and ejection of the substituent. 5-(m-Substituted) derivatives give mixtures of 5- and 6-substituted quinoxalines on pyrolysis.The 5-isomer is dominant for compounds with m-alkyl substituents, while the 6-isomer is the major product for those with electron-withdrawing or electron-donating m-substituents.
