13736-79-3

Basic information

• Product Name: 1-Methoxy-2-(Methylsulfonyl)benzene
• Synonyms: 1-Methoxy-2-(Methylsulfonyl)benzene
• CAS NO: 13736-79-3
• Molecular Formula: C₈H₁₀O₃S
• Molecular Weight: 186.2282
• Mol File: 13736-79-3.mol
• Article Data: 29

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-Methoxy-2-(Methylsulfonyl)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Methoxy-2-(Methylsulfonyl)benzene(13736-79-3)
• EPA Substance Registry System: 1-Methoxy-2-(Methylsulfonyl)benzene(13736-79-3)

Safety Data

• Hazardous Substances Data: 13736-79-3(Hazardous Substances Data)

Usage

Structure

A chemical compound consisting of a methoxy group (-OCH3) and a methylsulfonyl group (-SO2CH3) attached to a benzene ring.

Usage

Commonly used as a fragrance ingredient in perfumes and personal care products.

Odor

Possesses a sweet, floral, and slightly fruity odor.

Biological activities

Studied for its potential antimicrobial and anti-inflammatory properties.

Industrial application

Used as an intermediate in the production of other organic compounds and pharmaceuticals.

Stability

Considered to be relatively stable and non-reactive under normal conditions.

Versatility

Due to its stability and various properties, 1-Methoxy-2-(Methylsulfonyl)benzene is a useful chemical in different industries.

Upstream product

• 59057-32-8 Lithium 2-methoxybenzenesulfinate 
• 2388-73-0 1-methoxy-2-(methylsulfanyl)benzene 
• 36331-56-3 methoxybenzenesulfonyl hydrazide 
• 868-85-9 Dimethyl phosphite 
• 5896-95-7 5-Acetamino-2-methoxy-benzolsulfinsaeure 
• 7217-59-6 2-Methoxybenzenethiol 
• 75-75-2 methanesulfonic acid 
• 100-66-3 methoxybenzene 
• 13165-78-1 ortho-methoxybenzenesulfinic acid 
• 77-78-1 dimethyl sulfate 
• 38452-13-0 1-methylsulfinyl-2-methoxybenzene 
• 74-88-4 methyl iodide 
• 13736-78-2 4-methoxy-3-(methylsulfonyl)aniline 
• 17482-05-2 o-chlorophenyl methyl sulfone 

Downstream Products

• 75259-57-3 2-((2-methoxyphenyl)sulfonyl)ethanol 
• 56490-42-7 2-acetoxyphenyl methyl sulfone 
• 38063-41-1 1-methoxy-2-(methylsulfonyl)-4-nitrobenzene 
• 68276-74-4 3-(2-Methoxy-benzenesulfonyl)-propan-1-ol 
• 27489-33-4 2-hydroxyphenyl methyl sulfone 

Relevant articles and documents

Hydrophilic phase transfer catalyst based on the sulfoacid group and polyoxometalate for the selective oxidation of sulfides in water with hydrogen peroxide

A hybrid catalyst, based on SO3H-fuctionalized quaternary ammonium and polyoxovanadometalate, was synthesized and used for the selective oxidation of sulfides in water at room temperature. The highest turnover numbers (TON) can reach up to 1536. The organic products with high yields can be easily separated and the catalytic system can be used several times with the retention of catalytic activity.

High Chemoselectivity in the Construction of Aryl Methyl Sulfones via an Unexpected C-S Bond Formation between Sulfonylhydrazides and Dimethyl Phosphite

A highly chemoselective route to aryl methyl sulfones via an unexpected C S bond formation between sulfonylhydrazides and dimethyl phosphite catalyzed by NaI under mild conditions has been established. This transformation provides an alternative and metal-free pathway to acquire various aryl methyl sulfones in good to excellent yields. Notably, dimethyl phosphite was employed as a stable and readily available alkyl source.

A {Ti6W4}-Cluster-Substituted Polyoxotungstate: Synthesis, Structure, and Catalytic Oxidation Properties

A novel Ti-W-O-cluster-substituted tungstoantimonate (TA), [H2N(CH3)2]3Na4H9[{Ti6W4O18(OH)(H2O)3}(B-α-SbW9O33)3]·20H2O (1), has been made by hydrothermal reactions of trivacant [B-α-SbW9O33]9- units, Ti4+ cations, and WO42- anions in the presence of [H2N(CH3)2]·Cl and structurally characterized. Intriguingly, the polyoxoanion of 1 is constructed from three [B-α-SbW9O33]9- units and a previously unobserved decanuclear heterometallic Ti-W-O cluster [Ti6W4O18(OH)(H2O)3]11+ ({Ti6W4}) that is comprised of an octahedral [Ti6WO6(H2O)3]18+ cluster and an edge-sharing [W3O12(OH)]7- fragment via six W-O-Ti/W linkers. Furthermore, studies on the catalytic oxidation properties reveal that 1 possesses good catalytic activity toward the oxidation reactions of various sulfides and cyclooctene based on the environmentally friendly oxidant H2O2.