719-86-8 Usage
Uses
Used in Chemical Research:
2,4-Pyrrolidinedione, 3-acetyl-1-phenylis used as a research compound for exploring its chemical properties and potential applications in the field of chemistry. Its unique structure allows scientists to study its reactivity and interactions with other chemical entities.
Used in Synthetic Applications:
In the synthetic industry, 2,4-Pyrrolidinedione, 3-acetyl-1-phenylis employed as a synthetic intermediate for the production of various chemical compounds. Its specific functional groups and structural features make it a valuable building block in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Development:
2,4-Pyrrolidinedione, 3-acetyl-1-phenylis utilized as a key component in the development of new pharmaceuticals. Its unique structure and properties can be exploited to design and synthesize novel drug candidates with potential therapeutic applications.
Used in Material Science:
In the field of material science, 2,4-Pyrrolidinedione, 3-acetyl-1-phenylis employed as a component in the development of new materials with specific properties. Its chemical and physical characteristics can be harnessed to create materials with tailored properties for various applications, such as sensors, catalysts, or advanced materials for electronics and energy storage.
Check Digit Verification of cas no
The CAS Registry Mumber 719-86-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,1 and 9 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 719-86:
(5*7)+(4*1)+(3*9)+(2*8)+(1*6)=88
88 % 10 = 8
So 719-86-8 is a valid CAS Registry Number.
719-86-8Relevant academic research and scientific papers
Han, Chao,Guo, Yan-Chun,Wang, Dan-Dan,Dai, Xing-Jie,Wu, Feng-Juan,Liu, Huan-Fei,Dai, Gui-Fu,Tao, Jing-Chao
, p. 534 - 538 (2015)
A series of novel pyrazole fused heterocyclic derivatives were synthesized via a two-step procedure or a one-pot two step method, and their catalytic DNA cleavage abilities and anti-BVDV activities were also evaluated. The results obtained indicated that compounds 3b-3c could catalyze the cleavage of supercoiled DNA (pUC 19 plasmid DNA) to nicked DNA under physiological conditions with high yields via a hydrolytic mechanism. The studies on anti-viral activities against bovine viral diarrhea virus (BVDV) demonstrated that some of the pyrazole derivatives showed pronounced anti-BVDV activity with interesting EC50 values and no significant cytotoxicity. Among them, compound 3l showed the highest antiviral activity (EC50 = 0.12 μmol/L) and was 10 fold more than that of the positive control ribavirin (EC50 = 1.3 μmol/L), which provided a potential candidate for the development of anti-BVDV agents.
