22865-62-9 Usage
Description
4-(Methylsulfinyl)aniline is an aniline derivative with the molecular formula C8H9NO, featuring a methylsulfinyl group attached to the fourth position of the aromatic ring. It is a chemical compound that can be found in certain plant species and is known for its potential pharmacological properties, such as antioxidant and anti-inflammatory effects. 4-(Methylsulfinyl)aniline is commonly utilized in the synthesis of pharmaceuticals and organic compounds, and it may also contribute to the development of new drugs for various medical conditions. However, further research is necessary to fully comprehend its biological activities and potential therapeutic applications.
Uses
Used in Pharmaceutical Synthesis:
4-(Methylsulfinyl)aniline is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to be incorporated into the molecular structures of different drugs. Its presence in these compounds can potentially enhance their therapeutic effects and properties.
Used in Organic Compounds Synthesis:
As an aniline derivative, 4-(Methylsulfinyl)aniline is used as a building block in the synthesis of a range of organic compounds, contributing to the development of new chemical entities with diverse applications.
Used in Antioxidant and Anti-Inflammatory Research:
4-(Methylsulfinyl)aniline is used as a subject of study in research aimed at understanding its antioxidant and anti-inflammatory properties. These studies are crucial for exploring its potential use in the development of treatments for conditions associated with oxidative stress and inflammation.
Used in Drug Development:
4-(Methylsulfinyl)aniline is utilized in the development of new drugs for various medical conditions due to its potential pharmacological properties. Its role in this process is to provide a foundation for the creation of novel therapeutic agents that can address unmet medical needs.
Check Digit Verification of cas no
The CAS Registry Mumber 22865-62-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,8,6 and 5 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 22865-62:
(7*2)+(6*2)+(5*8)+(4*6)+(3*5)+(2*6)+(1*2)=119
119 % 10 = 9
So 22865-62-9 is a valid CAS Registry Number.
22865-62-9Relevant articles and documents
Catalyst-free visible light-mediated selective oxidation of sulfides into sulfoxides under clean conditions
Fan, Qiangwen,Zhu, Longwei,Li, Xuhuai,Ren, Huijun,Wu, Guorong,Zhu, Haibo,Sun, Wuji
supporting information, p. 7945 - 7949 (2021/11/01)
A facile and efficient visible-light-mediated method for directly converting sulfides into sulfoxides under clean conditions without using any photocatalysts is reported. This method exhibited favourable compatibility with functional groups and afforded a series of sulfoxides with high selectivity and yields. Moreover, in order to shed more light on such a transformation, detailed mechanism studies were carried out both experimentally and theoretically. The readily accessible, low-cost and eco-friendly nature of the developed method will endow it with attractive applications in chemical synthesis.
Alloxan-catalyzed biomimetic oxidations with hydrogen peroxide or molecular oxygen
Zhang, Shiqi,Li, Guangxun,Li, Ling,Deng, Xiongfei,Zhao, Gang,Cui, Xin,Tang, Zhuo
, p. 245 - 252 (2019/12/24)
Inspired by biological flavin catalysis, the nonionic alloxan derivatives were applied as the biomimetic catalysts for various oxidations, catalyzing oxidations of sulfides and amines with hydrogen peroxide or molecular oxygen under mild conditions with high yields in a short time. The whole catalytic cycle has been verified to be a biomimetic approach through the formation of the alloxan hydroperoxide reactive intermediate. Additionally, encouraging asymmetric catalytic results have been obtained with an easily prepared chiral alloxan in a sulfoxidation reaction.
Thioether Oxidation with H2O2 Catalyzed by Nb-Substituted Polyoxotungstates: Mechanistic Insights
Zalomaeva, Olga V.,Maksimchuk, Nataliya V.,Maksimov, Gennadii M.,Kholdeeva, Oxana A.
, p. 410 - 416 (2018/12/13)
Nb-monosubstituted polyoxotungstates of the Lindqvist and Keggin structures, (Bu4N)3[Nb(O)W5O18] (1) and (Bu4N)4[PW11NbO40] (2), respectively, catalyze oxidation of or
