73148-21-7 Usage
Uses
Used in Organic Synthesis:
8-Nitroquinoxalin-2(1H)-one is used as a key intermediate in the synthesis of various organic compounds and pharmaceuticals. Its unique structure and reactivity make it a valuable building block for the development of new molecules with potential applications in various industries.
Used in Medicinal Chemistry:
8-Nitroquinoxalin-2(1H)-one is used as a starting material for the development of new drugs and pharmaceutical agents. Its biological activities and potential as an antibacterial and antifungal agent make it a promising candidate for the treatment of various diseases and infections.
Used in Antibacterial Applications:
8-Nitroquinoxalin-2(1H)-one is used as an antibacterial agent for the treatment of bacterial infections. Its ability to inhibit the growth of bacteria makes it a valuable compound in the development of new antibiotics to combat drug-resistant strains.
Used in Antifungal Applications:
8-Nitroquinoxalin-2(1H)-one is used as an antifungal agent for the treatment of fungal infections. Its potential to inhibit the growth of fungi makes it a promising compound for the development of new antifungal drugs to address the increasing prevalence of drug-resistant fungal strains.
Used in Pharmaceutical Research:
8-Nitroquinoxalin-2(1H)-one is used as a research compound in the field of pharmaceuticals. Its unique properties and potential applications make it an important tool for studying the mechanisms of action, structure-activity relationships, and drug discovery.
Check Digit Verification of cas no
The CAS Registry Mumber 73148-21-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,1,4 and 8 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 73148-21:
(7*7)+(6*3)+(5*1)+(4*4)+(3*8)+(2*2)+(1*1)=117
117 % 10 = 7
So 73148-21-7 is a valid CAS Registry Number.
73148-21-7Relevant academic research and scientific papers
Synthesis and SAR of novel imidazoquinoxaline-based Lck inhibitors: Improvement of cell potency
Chen, Ping,Iwanowicz, Edwin J.,Norris, Derek,Gu, Henry H.,Lin, James,Moquin, Robert V.,Das, Jagabandhu,Wityak, John,Spergel, Steven H.,De Fex, Henry,Pang, Suhong,Pitt, Sydney,Shen, Ding Ren,Schieven, Gary L.,Barrish, Joel C.
, p. 3153 - 3156 (2007/10/03)
A series of anilino(imidazoquinoxaline) analogues bearing solubilizing side chains at the 6- and 7-positions of the fused phenyl ring has been prepared and evaluated for inhibition against Lck enzyme and of T-cell proliferation. Significant improvement of the cellular activity was achieved over the initial lead, compound 2.
o-Nitroaniline derivatives - 13. Reactions of N-(o-nitroaryl)sarcosine esters with bases
Collins,McFarlane,Mackie,Smith
, p. 7887 - 7898 (2007/10/02)
The title reactions give 1-hydroxy-4-methylquinoxaline-2,3-diones (4) together with a variety of mono- and bi-cyclic byproducts. All of these may result from a common intermediate, viz. a 1-hydroxy-4-methyl-3,4-dihydro-1H-2,1,4-benzoxadiazine-3-carboxylat
