532934-94-4 Usage
Uses
Used in Pharmaceutical Industry:
Quinoxaline, 7-chloro-5-methyl(9CI) is used as a key intermediate in the development of new drugs and therapies. Its unique structure and properties make it a promising candidate for creating innovative pharmaceutical compounds.
Used in Organic Synthesis:
In the field of organic synthesis, Quinoxaline, 7-chloro-5-methyl(9CI) serves as a valuable building block for the synthesis of more complex organic molecules, contributing to the advancement of chemical research and development.
Used in Materials Science:
Quinoxaline, 7-chloro-5-methyl(9CI) also finds applications in materials science, where its chemical and physical properties can be utilized to create new materials with specific characteristics for various applications.
Used in Research and Development:
Due to its unique structure and properties, Quinoxaline, 7-chloro-5-methyl(9CI) is suitable for research and development purposes, where it can be explored for potential new uses and applications across different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 532934-94-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,3,2,9,3 and 4 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 532934-94:
(8*5)+(7*3)+(6*2)+(5*9)+(4*3)+(3*4)+(2*9)+(1*4)=164
164 % 10 = 4
So 532934-94-4 is a valid CAS Registry Number.
532934-94-4Relevant academic research and scientific papers
Broad spectrum chemistry as practised by Novartis process research
Mickel, Stuart J.,Fischer, Reto,Marterer, Wolfgang
, p. 640 - 648 (2007/10/03)
Three actual examples from the current product palette within Novartis Process Research will demonstrate the some of the variety and challenges encountered in modern chemical development.
The nitration of 8-methylquinoxalines in mixed acid
Marterer, Wolfgang,Prikoszovich, Walter,Wiss, Jacques,Prashad, Mahavir
, p. 318 - 323 (2013/09/06)
8-Methylquinoxalines are nitrated surprisingly efficiently at C-5 following a simple nitration protocol with mixed acid at 40-50°C. The implications of halogen functionalisation at C-6 and modification of the mixed acid conditions on the relative rates of conversion and process safety are discussed. Competing side reactions for 6-halo-8-methylquinoxalines involve hydrolysis at C-6 and halogenation at C-7 or C-5.
