17508-35-9 Usage
Uses
Used in Pharmaceutical Research:
2(1H)-Quinoxalinone, 4-oxide is used as a potential therapeutic agent for its anticancer properties, targeting the inhibition of various cancer cell lines. It is being studied for its ability to combat different types of cancer, offering a new avenue for cancer treatment.
Used in Antimicrobial Applications:
As an antibacterial, antifungal, and antiviral agent, 2(1H)-Quinoxalinone, 4-oxide is used for its potential to treat infectious diseases by inhibiting the growth of harmful microorganisms, thereby providing a new approach to managing infections.
Used in Antioxidant Research:
2(1H)-Quinoxalinone, 4-oxide is used as an antioxidant, which may help in protecting cells from oxidative damage and could be beneficial in the development of treatments for diseases associated with oxidative stress.
Used in Immunomodulation:
2(1H)-Quinoxalinone, 4-oxide is used to modulate the immune response, which could be significant in the treatment of autoimmune diseases or conditions where the immune system's response needs to be fine-tuned for better health outcomes.
Check Digit Verification of cas no
The CAS Registry Mumber 17508-35-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,5,0 and 8 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 17508-35:
(7*1)+(6*7)+(5*5)+(4*0)+(3*8)+(2*3)+(1*5)=109
109 % 10 = 9
So 17508-35-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H6N2O2/c11-8-5-10(12)7-4-2-1-3-6(7)9-8/h1-5H,(H,9,11)
17508-35-9Relevant academic research and scientific papers
DERIVATIVES OF 3,4-DIHYDRO-3-THIOXO-2-QUINOXALINYLACETIC ACID
Toman, Jaromir,Klicnar, Jiri
, p. 419 - 428 (2007/10/02)
Ethyl 3,4-dihydro-4-methyl-3-thioxo-2-quinoxalinylacetate has been prepared by thionation of the 3-oxo derivative.The mechanism is discussed of the reaction of this ester with diethylamine giving the two non-isomerizing ketimine-enamine tautomers and 1,2-
REGIOSELECTIVE SYNTHESIS OF 2,6-DICHLOROQUINOXALINE AND 2-CHLORO-6-IODOQUINOXALINE
Sakata, Gozyo,Makino, Kenzi
, p. 323 - 326 (2007/10/02)
Facile regioselective synthesis of 2,6-dichloroquinoxaline and 2-chloro-6-iodoquinoxaline is described.Electrophilic substitution reaction of 2(1H)-quinoxalinone with chloride and iodide ion in 95percent sulfuric acid occurred at 6-position exclusively.
