67963-06-8

Usage

Uses

Used in Pharmaceutical Industry:
1-(Cyclohexylsulfonyl)-4-methylbenzene is used as a starting material for the synthesis of various pharmaceuticals. Its unique structure allows for the creation of a wide range of medicinal compounds, contributing to the development of new drugs and therapies.
Used in Agrochemical Industry:
In the agrochemical sector, 1-(cyclohexylsulfonyl)-4-methylbenzene serves as a key component in the production of various agrochemicals. Its versatility in chemical reactions enables the synthesis of compounds that can be used in pesticides, herbicides, and other agricultural products to enhance crop protection and yield.
Used in Material Science:
1-(Cyclohexylsulfonyl)-4-methylbenzene is also utilized in the field of materials science. Its chemical properties make it suitable for the development of new materials with specific characteristics, such as improved strength, durability, or chemical resistance.
Used in Dye and Pigment Production:
This versatile chemical compound is used in the production of dyes and pigments. Its ability to form a variety of chemical structures allows for the creation of a wide array of colors and shades, making it an essential component in the dye and pigment industry.
Used in Polymer Chemistry:
1-(Cyclohexylsulfonyl)-4-methylbenzene has applications in polymer chemistry, where it is used to synthesize polymers with specific properties. These polymers can be employed in various industries, such as plastics, coatings, and adhesives, due to their tailored characteristics.

Upstream product

• 59693-93-5 (4-methylphenyl)cyclohexyl sulfane 
• 824-79-3 sodium 4-methylbenzenesulfinate 
• 108-93-0 cyclohexanol 
• 126812-30-4 1,3-dioxoisoindolin-2-yl cyclohexanecarboxylate 
• 110-82-7 cyclohexane 
• 1576-35-8 toluene-4-sulfonic acid hydrazide 
• 106-45-6 para-thiocresol 
• 108-85-0 1-bromocyclohexane 
• 542-18-7 cyclohexyl chloride 
• 455-16-3 p-toluenesulfonyl fluoride 
• 931-51-1 cyclohexylmagnesiumchloride 
• 1146-49-2 <2-(p-tolylsulfonyl)hydrazino>cyclohexane 
• 14195-09-6 2-tosylcyclohexanone 

Downstream Products

• 106588-37-8 (1-deuterio-cyclohexyl)-p-tolyl sulfone 

Relevant academic research and scientific papers

Kinetic investigation on the highly efficient and selective oxidation of sulfides to sulfoxides and sulfones with t-BuOOH catalyzed by La2O3

The selective oxidation of various sulfides to sulfoxides by a simple, efficient, and environmentally benign method is of prime focus. In this paper, we have explored a highly efficient protocol for the oxidation of alkyl aryl sulfides to sulfoxides with high selectivities catalyzed by La2O3 in the presence of 70% t-BuOOH solution (water). We obtained predominantly the monooxygenated product. The over oxidation of sulfides to sulfones was not observed under these conditions. The resulting products are obtained in good to excellent yields within a reasonable time without the use of ligands and other additives. The epoxidation of the double bond as well as allylic oxidation are not observed with allyl sulfides. Sulfones can be obtained quantitatively by altering the reaction conditions. The surface morphology and the catalyst reusability were verified by XRD, AFM and SEM techniques. The surface area of the La2O3 was measured using BET isotherms.

Iron (III) chloride-catalyzed direct sulfonylation of alcohols with sodium arenesulfinates

A new protocol for the direct sulfonylation of benzylic, allylic and homoallylic alcohols with sodium arenesulfinates is described by using iron (III) chloride as a catalyst and chlorotrimethylsilane as an additive. This method requires no preactivation o

Organic reactions in ionic liquids: A new method for the synthesis of alkyl aryl sulfones by alkylation of sodium arenesulfinates with unactivated alkyl chlorides

A new method is reported for the synthesis of alkyl aryl sulfones by alkylation of sodium arenesulfinates with unactivated alkyl chlorides using ionic liquid based on 1-butyl-3-methylimidazolium tetrafluoroborate (BmimBF 4) mixed with water (2:1) as reaction media. The ionic liquid can be reused and the procedure gives the sulfones in moderate yields.

Sulfonylation of Organometallic Reagents with Arenesulfonyl Fluorides: A Simple One-Step Synthesis of Sulfones

Sulfonylation of organometallic reagents was accomplished with arenesulfonyl fluorides to provide a wide variety of alkylaryl- and diaryl sulfones.Organolithium and diorganocopper lithium reagents react smoothly with arenesulfonyl fluorides to give sulfones in high yields.Alkyl Grignard reagents often lead to mixtures of monosulfonylated and disulfonylated products.However, allylmagnesium chloride and phenylmagnesium chloride provide the corresponding sulfones in excellent yields.Organocopper reagents were also found to yield sulfones upon treatment with arenesulfonyl fluorides.By utilizing this methodology, synthetically useful alkyl, (trimethylsilyl)methyl, and allyl sulfones are easily prepared in high yields.