61522-56-3 Usage
Uses
Used in Pharmaceutical Industry:
Ethanone, 1-(3-methyl-4-oxido-2-quinoxalinyl)is utilized as a pharmaceutical agent for its anti-inflammatory and analgesic properties. Its unique chemical structure allows it to modulate biological pathways involved in inflammation and pain, making it a promising candidate for the development of new medications to treat various inflammatory and painful conditions.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, Ethanone, 1-(3-methyl-4-oxido-2-quinoxalinyl)serves as a valuable compound for research and development. Its distinctive structure and pharmacological properties provide a foundation for the design and synthesis of novel therapeutic agents with improved efficacy and reduced side effects.
Used in Drug Delivery Systems:
To enhance the bioavailability and therapeutic efficacy of Ethanone, 1-(3-methyl-4-oxido-2-quinoxalinyl)-, various drug delivery systems are being explored. These systems aim to improve the compound's solubility, stability, and targeted delivery to specific tissues or cells, thereby optimizing its pharmacological effects and minimizing potential side effects.
Check Digit Verification of cas no
The CAS Registry Mumber 61522-56-3 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 6 respectively.
Calculate Digit Verification of CAS Registry Number 61522-56:
(7*6)+(6*1)+(5*5)+(4*2)+(3*2)+(2*5)+(1*6)=103
103 % 10 = 3
So 61522-56-3 is a valid CAS Registry Number.
61522-56-3Relevant 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.
