6178-26-3

Basic information

• Product Name: Benzene, 1-chloro-4-[[(1E)-2-(4-chlorophenyl)ethenyl]sulfonyl]-
• CAS NO: 6178-26-3
• Molecular Formula: C14H10Cl2O2S
• Molecular Weight: 313.204
• Mol File: 6178-26-3.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: Benzene, 1-chloro-4-[[(1E)-2-(4-chlorophenyl)ethenyl]sulfonyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-chloro-4-[[(1E)-2-(4-chlorophenyl)ethenyl]sulfonyl]-(6178-26-3)
• EPA Substance Registry System: Benzene, 1-chloro-4-[[(1E)-2-(4-chlorophenyl)ethenyl]sulfonyl]-(6178-26-3)

Safety Data

• Hazardous Substances Data: 6178-26-3(Hazardous Substances Data)

Upstream product

• 6510-80-1 (4-chloro-phenyl)-(4-chloro-trans-styryl)-sulfide 
• 3405-89-8 2-(4-chloro-phenylsulfonyl)acetic acid 
• 104-88-1 4-chlorobenzaldehyde 
• 1615-02-7 3-(4-chlorophenyl)prop-2-enoic acid 
• 1146-44-7 4,4'-dichlorophenyl thiosulfonate 
• 1073-67-2 4-vinylbenzyl chloride 
• 706-07-0 1-chloro-4-(2-nitrovinyl)benzene 
• 14752-66-0 sodium p-chlorobenzenesulphinate 
• 69770-58-7 diethyl<<(p-chlorophenyl)sulfide>methyl>phosphonate 
• 40137-12-0 diethyl<<(p-chlorophenyl)sulfonyl>methyl>phosphonate 
• 106-54-7 p-Chlorothiophenol 
• 873-73-4 4-n-chlorophenylacetylene 
• 98-60-2 4-chlorobenzenesulfonyl chloride 

Downstream Products

• 1097725-24-0 methyl 4-(4-chlorophenylsulfonyl)-3-(4-chlorophenyl)butyrate 
• 86432-70-4 C₁₅H₁₂Cl₂O₂S 

Relevant articles and documents

Synthesis of Vinyl Sulfones via I2-mediated Alkene Sulfonylations with Thiosulfonates

A simple sulfonylation strategy involving I2 and thiosulfonates, as sulfonyl-group precursors, is reported for the synthesis of vinyl sulfones. Sulfonyl radicals are presumed to be generated from thiosulfonates, which subsequently react with st

Metal-free iodine-mediated synthesis of vinyl sulfones at room temperature using water as solvent

Metal-free efficient iodine-mediated synthesis of vinyl sulfones utilizing aryl sulfinates and alkenes has been realized under mild conditions in water. Notably, sodium methanesulfinate was used in this transformation, affording the β-iodo sulfones in goo

(E)-4-carboxystyrl-4-chlorobenzyl sulfone and pharmaceutical compositions thereof

Pre-treatment with α,β unsaturated aryl sulfones protects normal cells from the cytotoxic side effects of two classes of anticancer chemotherapeutics. Administration of a cytoprotective sulfone compound to a patient prior to anticancer chemotherapy with a