32361-73-2

Basic information

• Product Name: Ethanone, 1-[4-(methylsulfinyl)phenyl]-
• Synonyms: (4-acetophenyl) methylsulfoxide;4'-(methylsulfinyl)acetophenone;4-(methylsulfinyl)-acetophenone;1-(4-methansulfinylphenyl)ethanon;1-(4-methansulfinylphenyl)ethanone;1-(4-methansulfinylphenyl)-ethanone
• CAS NO: 32361-73-2
• Molecular Formula: C9H10O2S
• Molecular Weight: 182.243
• Mol File: 32361-73-2.mol
• Article Data: 92

Chemical Properties

• CAS DataBase Reference: Ethanone, 1-[4-(methylsulfinyl)phenyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 1-[4-(methylsulfinyl)phenyl]-(32361-73-2)
• EPA Substance Registry System: Ethanone, 1-[4-(methylsulfinyl)phenyl]-(32361-73-2)

Safety Data

• Hazardous Substances Data: 32361-73-2(Hazardous Substances Data)

Usage

General Description

Ethanone, 1-[4-(methylsulfinyl)phenyl]-, also known as sulfoxide, is an organic compound with the molecular formula C9H10O2S. It is a derivative of the organic group methylsulfinyl phenyl and is commonly used in the production of pharmaceuticals and agrochemicals. This chemical compound is known for its strong odor and is used in the manufacturing of perfumes and fragrances. It is also used as a solvent in various industries and has potential applications in the field of medicinal chemistry due to its unique chemical properties.

Upstream product

• 99-92-3 p-aminobenzophenone 
• 67-68-5 dimethyl sulfoxide 
• 3446-89-7 4-(Methylthio)benzaldehyde 
• 1778-09-2 4-(Methylthio)acetophenone 
• 144-86-5 N-chloro-4-methylbenzenesulfonamide 

Downstream Products

• 92017-04-4 (4-acetyl-phenylsulfanyl)-acetic acid methyl ester 
• 1330184-65-0 N-[(4-acetylphenyl)(methyl)(oxo)-λ⁶-sulfanylidene]cyanamide 
• 1620443-54-0 (4-acetylphenyl)(imino)(methyl)-λ⁶-sulfanone 
• 1778-09-2 4-(Methylthio)acetophenone 
• 126937-17-5 Acetic acid [1-(4-methanesulfinyl-phenyl)-eth-(E)-ylidene]-hydrazide 
• 10297-73-1 4-(methanesulfonyl)acetophenone 

Relevant articles and documents

The sulfoxidation reaction catalyzed by CoBr2 complexes, under the magnifying glass of green parameters

Different cobalt (II) and nickel (II) species were used as catalysts in sulfoxidation reactions giving excellent yields and high chemoselectivity. Among the cobalt (II) species, both γ-cyclodextrin complexes synthesized in ethyl acetate or dichloromethane solvents were very good catalysts, while γCDNiBr2 synthesized in ethyl acetate was the best of Ni (II) species. Sulfoxidation takes place with high chemoselectivity in the presence of other groups such as aldehyde. Good results were obtained when these reactions were analyzed using green chemistry metrics. Techniques as FT-IR, UV–vis Diffuse Reflectance, colorimetry, TGA, flame atomic absorption, potentiometric halide titration, and elemental analysis were used to characterize novel complexes. The change of solvent in the synthesis of complexes produces positive effects in holistic green metrics.

Borate-catalyzed reactions of hydrogen peroxide: Kinetics and mechanism of the oxidation of organic sulfides by peroxoborates

The kinetics of the oxidation of substituted phenyl methyl sulfides by hydrogen peroxide in borate/boric acid buffers were investigated as a function of pH, total peroxide concentration, and total boron concentration. Second-order rate constants at 25°C f

An efficient and selective photocatalytic system for the oxidation of sulfides to sulfoxides

A heterogenous nation membrane containing lead ruthenate pyrochlore (Pyc) and [Ru(bpy)3]2+ (designated as | NPyc-Ru(bpy)|) photochemically catalyzes the selective oxidation of organic sulfide to sulfoxide in the presence o

Synergistic cooperative effect of CF3SO2Na and bis(2-butoxyethyl)ether towards selective oxygenation of sulfides with molecular oxygen under visible-light irradiation

A safe, practical and eco-friendly method for the switchable synthesis of sulfoxides and sulfones through visible-light-initiated oxygenation of sulfides at ambient temperature under transition-metal-, additives-free and minimal solvent conditions. The synergistic catalytic efforts between CF3SO2Na and 2-butoxyethyl ether represents the key promoting factor for the reaction. This journal is

Electrochemical oxygenation of sulfides with molecular oxygen or water: Switchable preparation of sulfoxides and sulfones

A practical and eco-friendly method for the controllable aerobic oxygenation of sulfides by electrochemical catalysis was developed. The switchable preparation of sulfoxides and sulfones was effectively controlled by reaction time, in which both molecular oxygen and water can be used as the oxygen source under catalyst and external oxidant-free conditions. The electrochemical protocol features a broad substrate scope and excellent site selectivity and is successfully applied to the modification of some sulfide-containing pharmaceuticals and their derivatives. This journal is

Electrochemical Scalable Sulfoxidation of Sulfides with Molecular Oxygen and Water

An efficient and chemoselective synthesis of sulfoxides through the electrooxidation of sulfides has been well developed. This protocol takes advantage of electricity as the terminal oxidant and of molecular oxygen and water as the oxygen atom sources. A variety of structurally diverse sulfoxide compounds are assembled in moderate to excellent yields. The scaled-up reactions at 6–20 mmol show the good practicability and application potential of this methodology. A possible free radical mechanism has been proposed to rationalize the reaction procedure.