61522-57-4 Usage
Uses
Used in Pharmaceutical Synthesis:
Ethanone, 1-(3-methyl-1-oxido-2-quinoxalinyl)is utilized as an intermediate in the synthesis of pharmaceuticals, contributing to the development of new drugs. Its chemical structure allows for the creation of complex molecules with potential therapeutic applications.
Used in Agrochemical Production:
Ethanone, 1-(3-methyl-1-oxido-2-quinoxalinyl)is also employed in the production of agrochemicals, where it may serve as a key component in the formulation of pesticides or other agricultural products. Its role in these applications is to enhance the effectiveness of the final product, ensuring better crop protection and yield.
Used in Chemical Research:
Ethanone, 1-(3-methyl-1-oxido-2-quinoxalinyl)is used as a research tool in the field of chemistry, particularly in studies focused on the synthesis and properties of quinoxaline-based compounds. Its unique structure provides a platform for exploring new reaction pathways and understanding the behavior of similar molecules.
Potential Biological Activities:
While not yet fully understood, Ethanone, 1-(3-methyl-1-oxido-2-quinoxalinyl)may exhibit biological activities that could be harnessed for various applications. Ongoing research aims to uncover these potential properties, which could lead to new uses in medicine, agriculture, or other industries.
Check Digit Verification of cas no
The CAS Registry Mumber 61522-57-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,5,2 and 2 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 61522-57:
(7*6)+(6*1)+(5*5)+(4*2)+(3*2)+(2*5)+(1*7)=104
104 % 10 = 4
So 61522-57-4 is a valid CAS Registry Number.
61522-57-4Relevant academic research and scientific papers
REACTIONS OF 2-ACETYL-3-METHYLQUINOXALINE 1,4-DIOXIDE AND ITS DERIVATIVES
Matoba, Katsuhide,Terada, Takashi,Sugiura, Masaru
, p. 55 - 58 (2007/10/02)
2-Cinnamoyl-3-methylquinoxaline 1,4-dioxide (2) was inert to hydrochloric acid in refluxing ethanol.When a xylene solution of 2-acetyl-3-methylquinoxaline 1,4-dioxide (1-dioxide) was refluxed overnight, the dioxide was reduced mainly to 1,4-oxide and the oxidative products from xylene were also obtained. 2-Cinnamoyl-3-methylquinoxaline 4-oxide (4a) and 3-methyl-4-oxido-2-quinoxalyl 4-phenyl-1,3-butadienyl ketone (4b) were quantitatively cyclized into 4-methyl-3-oxo-1-phenyl- and 4-methyl-3-oxo-1-styryl-3H-pyrroloquinoxalin-10-ium chloride (6a and 6 b), respectively , when the ethanolic solution were refluxed in the presence of hydrochloric acid.
