90556-95-9 Usage
Uses
Used in Pharmaceutical Industry:
2-(pyridin-2-yl)-1,2-thiazinane 1,1-dioxide is used as a pharmaceutical compound for its potential therapeutic applications in treating various medical conditions. Its unique structure and properties make it a candidate for further research and development in drug discovery.
Used in Antimicrobial Applications:
In the field of antimicrobial research, 2-(pyridin-2-yl)-1,2-thiazinane 1,1-dioxide is utilized for its potential to combat microbial infections. Its antimicrobial properties are being studied to understand its effectiveness against different types of pathogens, which could lead to the development of new antimicrobial agents.
Used in Anticancer Applications:
2-(pyridin-2-yl)-1,2-thiazinane 1,1-dioxide is also being explored for its potential as an anticancer agent. Its biological activities are under investigation to determine its impact on cancer cells and its ability to inhibit tumor growth, which could contribute to the development of novel cancer therapies.
Used in Medicinal Chemistry Research:
In the realm of medicinal chemistry, 2-(pyridin-2-yl)-1,2-thiazinane 1,1-dioxide serves as a versatile compound for research. Its unique structure and potential biological activities make it a valuable subject for studies aimed at understanding its mechanisms of action and optimizing its properties for various therapeutic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 90556-95-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,5,5 and 6 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 90556-95:
(7*9)+(6*0)+(5*5)+(4*5)+(3*6)+(2*9)+(1*5)=149
149 % 10 = 9
So 90556-95-9 is a valid CAS Registry Number.
90556-95-9Relevant academic research and scientific papers
Cross coupling of 3-bromopyridine and sulfonamides (R1NHSO2R2·R1 = H, Me, alkyl; R2 = alkyl and aryl) catalyzed by CuI/1,3-di(pyridin-2-yl)propane-1,3-dione
Han, Xiaojun
experimental part, p. 360 - 362 (2010/03/24)
N-(3-Pyridinyl)-substituted secondary and tertiary sulfonamides have been synthesized in good to excellent yields by the reaction of 3-bromopyridine with primary and secondary alkyl and aryl sulfonamides (MeSO2NH2, MeSO2NHMe, TolSO2NH2, TolSO2NHMe, 1,3-propanesultam, and 1,4-butanesultam), catalyzed by CuI (20 mol %) and 1,3-di(pyridin-2-yl)propane-1,3-dione (20 mol %) with K2CO3 (200 mol %) in DMF (0.17 M for ArBr) at 110-120 °C over 36-40 h. 2-Bromopyridine, 4-bromopyridine, and a wide variety of substituted phenyl bromides can also be successfully coupled with sulfonamides under these reaction conditions.
Synthesis of N-arylated sultams: Palladium- and copper-catalyzed cross coupling of aryl halides with 1,4-butane and 1,3-propanesultams
Steinhuebel, Dietrich,Palucki, Michael,Askin, David,Dolling, Ulf
, p. 3305 - 3307 (2007/10/03)
Palladium-catalyzed cross coupling of 1,4-butanesultam and 1,3-propanesultam with a variety of aryl halides was found to provide the desired products in 62-93% isolated yield using Xantphos as ligand. The Pd-catalyzed reaction was found to be superior to the analogous Cu-catalyzed reaction based on product yields, reaction rates, and substrate scope.
