22865-62-9

Basic information

• Product Name: 4-(Methylsulfinyl)aniline
• Synonyms: 4-(Methylsulfinyl)aniline;4-(methylsulfinyl)benzenamine
• CAS NO: 22865-62-9
• Molecular Formula: C₇H₉NOS
• Molecular Weight: 155.21746
• Mol File: 22865-62-9.mol
• Article Data: 43

Chemical Properties

• Boiling Point: 353.9±25.0 °C(Predicted)
• Appearance: /
• Density: 1.28±0.1 g/cm3(Predicted)
• PKA: 2.73±0.10(Predicted)
• CAS DataBase Reference: 4-(Methylsulfinyl)aniline(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(Methylsulfinyl)aniline(22865-62-9)
• EPA Substance Registry System: 4-(Methylsulfinyl)aniline(22865-62-9)

Safety Data

• Hazardous Substances Data: 22865-62-9(Hazardous Substances Data)

Usage

General Description

4-(Methylsulfinyl)aniline is a chemical compound with the molecular formula C8H9NO. It is an aniline derivative with a methylsulfinyl group attached to the fourth position of the aromatic ring. 4-(Methylsulfinyl)aniline can be found in certain plant species and is commonly used in the synthesis of pharmaceuticals and organic compounds. It has been studied for its potential pharmacological properties, including its antioxidant and anti-inflammatory effects. 4-(Methylsulfinyl)aniline may also have applications in the development of new drugs for various medical conditions. However, further research is needed to fully understand its biological activities and potential therapeutic uses.

Upstream product

• 104-96-1 4-methylsulfanylaniline 
• 540-37-4 p-aminoiodobenzene 
• 124-43-6 urea hydrogen peroxide adduct 
• 940-12-5 p-nitrophenyl methyl sulfoxide 
• 73475-07-7 isoaalloxazine hydroperoxide 
• 2976-30-9 1-methanesulfonyl-4-nitrobenzene 

Downstream Products

• 265114-14-5 N-(4-Fluorobenzyliden)-4-methylsulfinylaniline 
• 361486-22-8 N-(4-fluoro-3-methoxybenzyliden)-4-methylsulfinylaniline 
• 51791-02-7 2-Chlor-3-p-methylsulfinylphenylpropionitril 
• 104-96-1 4-methylsulfanylaniline 
• 1586823-26-8 3-(N-(5-chloropyridin-2-yl)-N-methylsulfamoyl)-N-(4-(methylsulfinyl)phenyl)benzamide 
• 1586823-21-3 3-(N-(4-cyanophenyl)-N-methylsulfamoyl)-4-methoxy-N-(4-(methylsulfinyl)phenyl)benzamide 
• 1586823-17-7 3-(N-methyl-N-(4-(methylsulfonyl)phenyl)sulfamoyl)-N-(4-(methylsulfinyl)phenyl)benzamide 
• 1586823-13-3 3-(N-methyl-N-(4-(methylsulfinyl)phenyl)sulfamoyl)-N-(4-(methylsulfinyl)phenyl)benzamide 
• 1586823-06-4 3-(N-(4-acetylphenyl)-N-methylsulfamoyl)-N-(4-(methylsulfinyl)phenyl)benzamide 
• 1586822-97-0 3-(N-(4-cyanophenyl)-N-methylsulfamoyl)-N-(4-(methylsulfinyl)phenyl)benzamide 
• 1586822-63-0 3-(N-(4-chlorophenyl)-N-methylsulfamoyl)-N-(4-(methylsulfinyl)phenyl)benzamide 
• 1586822-49-2 3-(N-(4-fluorophenyl)-N-methylsulfamoyl)-N-(4-(methylsulfinyl)phenyl)benzamide 
• 51791-04-9 trans-p-Methylsulphinylcinnamamidoxime 
• 51791-03-8 trans-p-Methylsulfinylcinnamonitril 

Relevant articles and documents

Catalyst-free visible light-mediated selective oxidation of sulfides into sulfoxides under clean conditions

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

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

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