Production Method 1

96088-58-3

3112-85-4

96088-61-8

80-18-2

Reaction Conditions

Reference

Mesylhydroxylamines. VI. Oxidation of N-mesylhydroxylamines - vibrational spectra and crystal structure of 1,2-dimesyl-1,2-dimethoxyhydrazine

Brink, Klaus; et al, Chemische Berichte, 1985, 118(2), 564-73

Production Method 2

3729-53-1

3112-85-4

96088-61-8

80-18-2

Reaction Conditions

1.1 Reagents: Lead dioxide Solvents: Dichloromethane
2.1 -

Reference

Mesylhydroxylamines. VI. Oxidation of N-mesylhydroxylamines - vibrational spectra and crystal structure of 1,2-dimesyl-1,2-dimethoxyhydrazine

Brink, Klaus; et al, Chemische Berichte, 1985, 118(2), 564-73

Methyl phenyl sulfone Raw materials

• Benzenesulfonamide,N-methoxy-
• Benzenesulfonamide, N-methoxy-N-[methoxy(phenylsulfonyl)amino]-

Methyl phenyl sulfone Preparation Products

• Benzenesulfonamide, N-methoxy-N-(phenylsulfonyl)- (96088-61-8)
• Methyl benzenesulfonate (80-18-2)
• Methyl phenyl sulfone (3112-85-4)

• 1. Enantioselective sulfoxidation using Streptomyces glaucescens GLA.0
  Sara Salama,Tarek Dishisha,Mohamed H. Habib,Ahmed Z. Abdelazem,Walid Bakeer,Mahmoud Abdel-Latif,Yasser Gaber RSC Adv. 2020 10 32335
• 2. Ti(iv)-amino triphenolate complexes as effective catalysts for sulfoxidation
  Miriam Mba,Leonard J. Prins,Cristiano Zonta,Massimo Cametti,Arto Valkonen,Kari Rissanen,Giulia Licini Dalton Trans. 2010 39 7384
• 3. Highly efficient oxidation of various thioethers catalyzed by organic ligand-modified polyoxomolybdates
  Haiyan An,Yujiao Hou,Shenzhen Chang,Jie Zhang,Qingshan Zhu Inorg. Chem. Front. 2020 7 169
• 4. Enantioselective copper catalysed intramolecular C–H insertion reactions of α-diazo-β-keto sulfones, α-diazo-β-keto phosphine oxides and 2-diazo-1,3-diketones; the influence of the carbene substituent
  Amy E. Shiely,Catherine N. Slattery,Alan Ford,Kevin S. Eccles,Simon E. Lawrence,Anita R. Maguire Org. Biomol. Chem. 2017 15 2609
• 5. A comparative evaluation of the voltammetric behaviour of phenyl methyl sulfone, phenyl methyl sulfide and phenyl methyl sulfoxide in N, N-dimethylformamide on a glassy carbon electrode
  Subbiah Chellammal,Michael Noel,Payyallar Narayanan Anantharaman J. Chem. Soc. Perkin Trans. 2 1993 993

• Solvents and Organic Chemicals Organic Compounds Benzenoids Benzene and substituted derivatives Benzenesulfonyl compounds
• Solvents and Organic Chemicals Organic Compounds

Methyl phenyl sulfone (CAS No. 3112-85-4): A Comprehensive Overview

Methyl phenyl sulfone, chemically identified by the CAS number 3112-85-4, is a significant compound in the realm of chemical and pharmaceutical research. This organosulfur compound, characterized by its methyl and phenyl sulfone functional groups, has garnered considerable attention due to its versatile applications and emerging roles in medicinal chemistry. The molecular structure of methyl phenyl sulfone consists of a sulfone moiety linked to a phenyl ring, with a methyl group attached, making it a valuable intermediate in synthetic chemistry and drug development.

The< strong>methyl phenyl sulfone molecule exhibits unique chemical properties that make it a promising candidate for various industrial and pharmaceutical applications. Its stability under different conditions and reactivity with other compounds have positioned it as a key player in the synthesis of complex molecules. Recent studies have highlighted its potential in the development of novel therapeutic agents, particularly in the treatment of inflammatory diseases and cancer.

In the context of pharmaceutical research, methyl phenyl sulfone has been extensively studied for its anti-inflammatory and antioxidant properties. The sulfone group is known to exhibit significant biological activity, making it an attractive scaffold for drug design. Researchers have leveraged this property to develop derivatives of methyl phenyl sulfone that exhibit enhanced efficacy and reduced side effects compared to existing treatments. For instance, studies have shown that certain derivatives of this compound can modulate inflammatory pathways by inhibiting key enzymes such as COX-2 and LOX.

The< strong>CAS No. 3112-85-4 identifier ensures that researchers worldwide can accurately reference and utilize this compound in their experiments. The systematic naming convention provided by CAS numbers is crucial for maintaining consistency and clarity in scientific literature. This standardization allows for seamless communication among scientists, facilitating collaborative research and accelerating the discovery of new therapeutic strategies.

Recent advancements in computational chemistry have further enhanced the understanding of methyl phenyl sulfone's interactions with biological targets. Molecular modeling techniques have been employed to predict how this compound binds to specific proteins and enzymes, providing insights into its mechanism of action. These computational studies have complemented experimental approaches, leading to a more comprehensive understanding of its pharmacological properties.

The< strong>methyl phenyl sulfone market has seen significant growth due to its increasing applications in pharmaceuticals and agrochemicals. Manufacturers specializing in fine chemicals have expanded their production capabilities to meet the growing demand for this compound. The synthesis of methyl phenyl sulfone has been optimized through various chemical pathways, ensuring high yield and purity levels suitable for industrial use.

In addition to its therapeutic potential, methyl phenyl sulfone has been explored for its role in material science. Its unique chemical structure makes it a suitable candidate for developing advanced materials with specific properties such as conductivity and biodegradability. Researchers are investigating its incorporation into polymers and coatings to enhance their performance under various environmental conditions.

The< strong>CAS No. 3112-85-4 classification ensures that all regulatory requirements are met when handling and distributing this compound. Compliance with safety guidelines is paramount to ensure the well-being of researchers and industrial workers involved in its production and application.

The future prospects of methyl phenyl sulfone look promising, with ongoing research aimed at uncovering new applications and improving existing formulations. The integration of artificial intelligence (AI) into drug discovery processes has expedited the identification of novel derivatives with enhanced pharmacological properties. AI-driven platforms can analyze vast datasets to predict the efficacy of compounds like methyl phenyl sulfone, thereby reducing the time required for drug development.

In conclusion, methyl phenyl sulfone (CAS No. 3112-85-4) is a multifaceted compound with significant implications in pharmaceuticals, material science, and beyond. Its unique chemical properties and biological activities make it a valuable asset in modern research and industry. As scientific understanding continues to evolve, the applications of this compound are expected to expand, contributing to advancements in medicine and technology.

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