21383-00-6

Basic information

• Product Name: 3-CHLOROPHENYLMETHYLSULFONE
• Synonyms: 3-CHLOROPHENYLMETHYLSULFONE
• CAS NO: 21383-00-6
• Molecular Formula: C₇H₇ClO₂S
• Molecular Weight: 190.65
• Mol File: 21383-00-6.mol
• Article Data: 28

Chemical Properties

• Melting Point: 108-109°C
• Appearance: /
• CAS DataBase Reference: 3-CHLOROPHENYLMETHYLSULFONE(CAS DataBase Reference)
• NIST Chemistry Reference: 3-CHLOROPHENYLMETHYLSULFONE(21383-00-6)
• EPA Substance Registry System: 3-CHLOROPHENYLMETHYLSULFONE(21383-00-6)

Safety Data

• Hazardous Substances Data: 21383-00-6(Hazardous Substances Data)

Usage

General Description

3-Chlorophenylmethylsulfone, also known as Chlormezanone, is a chemical compound with the molecular formula C7H7ClO2S. It is a white, crystalline solid that is used as a muscle relaxant and anxiolytic medication. 3-Chlorophenylmethylsulfone works by affecting the central nervous system, causing muscle relaxation and sedation. It is commonly used in the treatment of muscle spasms and anxiety, and has also been investigated for use in the management of alcohol withdrawal. However, its use has been limited in some countries due to concerns about potential side effects and abuse potential. Overall, 3-Chlorophenylmethylsulfone is a chemical with important therapeutic uses, but caution is required in its administration and monitoring for adverse effects.

Upstream product

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Downstream Products

• 15946-37-9 sodium 3-chlorobenzenesulfinate 

Relevant articles and documents

Evidence for a Perepoxide Intermediate in the 1,2-Cycloaddition of Singlet Oxygen to Adamantylideneadamantane: Nucleophilic Oxygen Atom Transfer to Sulfoxides

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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

Flow Electrosynthesis of Sulfoxides, Sulfones, and Sulfoximines without Supporting Electrolytes

An efficient electrochemical flow process for the selective oxidation of sulfides to sulfoxides and sulfones and of sulfoxides toN-cyanosulfoximines has been developed. In total, 69 examples of sulfoxides, sulfones, andN-cyanosulfoximines have been synthesized in good to excellent yields and with high current efficiencies. The synthesis was assisted and facilitated through a supporting electrolyte-free, fully automated electrochemical protocol that highlights the advantages of flow electrolysis.