105971-70-8

Basic information

• Product Name: Benzene, 1-chloro-2-[[(4-chlorophenyl)sulfonyl]methyl]-
• CAS NO: 105971-70-8
• Molecular Formula: C13H10Cl2O2S
• Molecular Weight: 301.193
• Mol File: 105971-70-8.mol

Chemical Properties

• CAS DataBase Reference: Benzene, 1-chloro-2-[[(4-chlorophenyl)sulfonyl]methyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-chloro-2-[[(4-chlorophenyl)sulfonyl]methyl]-(105971-70-8)
• EPA Substance Registry System: Benzene, 1-chloro-2-[[(4-chlorophenyl)sulfonyl]methyl]-(105971-70-8)

Safety Data

• Hazardous Substances Data: 105971-70-8(Hazardous Substances Data)

Upstream product

• 14752-66-0 sodium p-chlorobenzenesulphinate 
• 611-17-6 1-bromomethyl-2-chlorobenzene 
• 735327-53-4 (2-chloro-benzyl)-(4-chloro-phenyl)-sulfide 

Downstream Products

• 558462-09-2 1-Chloro-2-[1-((4-chlorophenyl)sulfonyl]-5-(methylsulfonyl)pentyl]benzene 

Relevant articles and documents

Selective oxidation of sulfides to sulfoxides and sulfones using n-butyltriphenylphosphonium dichromate (BunPPh3) 2Cr2O7 in the presence of aluminium chloride in solution and under microwave irradiation

A wide variety of sulfides are efficiently oxidized to their corresponding sulfoxides and sulfones in excellent yields using n-butyltriphenylphosphonium dichromate (BTPPDC) in the presence of aluminium chloride in acetonitrile solution and under microwave irradiation. In addition, selective oxidation of sulfides in the presence of functional groups such as a carbon-carbon double bond, ketone, oxime, aldehyde, ether, and acetal can be considered as a noteworthy advantage of this method. Copyright Taylor & Francis Inc.

3-Carboxypyridinium chlorochromate - aluminium chloride - An efficient and inexpensive reagent system for the selective oxidation of sulfides to sulfoxides and sulfones in solution and under microwave irradiation

3-Carboxypyridinium chlorochromate (CPCC) in the presence of aluminium chloride is a very efficient reagent for the selective oxidation of sulfides to sulfoxide and sulfones in solution and under microwave irradiation. It is noteworthy that different functional groups including carbon-carbon double bonds, ketones, oximes, aldehydes, ethers, and acetals were tolerated under these reaction conditions.

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