26189-62-8

Basic information

• Product Name: [1-phenyl-2-(phenylsulfonyl)vinyl]benzene
• Synonyms: [1-phenyl-2-(phenylsulfonyl)vinyl]benzene
• CAS NO: 26189-62-8
• Molecular Formula: C₂₀H₁₆O₂S
• Molecular Weight: 320.40484
• Mol File: 26189-62-8.mol
• Article Data: 50

Chemical Properties

• Appearance: /
• CAS DataBase Reference: [1-phenyl-2-(phenylsulfonyl)vinyl]benzene(CAS DataBase Reference)
• NIST Chemistry Reference: [1-phenyl-2-(phenylsulfonyl)vinyl]benzene(26189-62-8)
• EPA Substance Registry System: [1-phenyl-2-(phenylsulfonyl)vinyl]benzene(26189-62-8)

Safety Data

• Hazardous Substances Data: 26189-62-8(Hazardous Substances Data)

Upstream product

• 3220-49-3 phenyl copper 
• 58202-72-5 (E)-((1-iodo-2-(phenylsulfonyl)vinyl))benzene 
• 119-61-9 benzophenone 
• 17872-92-3 (phenylsulfonylmethyl)trimethylsilane 
• 97399-03-6 benzenesulfonylmethane 
• 116511-95-6 (benzenesulfonyl)methyllithium 
• 26186-79-8 mercuric benzenesulfinate 
• 67341-86-0 Ph₂CCHHgBr 
• 530-48-3 1,1-Diphenylethylene 
• 98-09-9 benzenesulfonyl chloride 
• 23975-23-7 2-benzenesulfinyl-1,1-diphenylethanol 
• 100-34-5 benzene diazonium chloride 
• 19997-66-1 1-iodo-2,2-diphenylethylene 
• 16212-06-9 phenyl styryl sulfone 

Downstream Products

• 5433-76-1 diphenylmethyl phenyl sulfone 
• 91083-83-9 1-cyclohexyl-2,2’-diphenylethene 
• 35467-39-1 1,1-diphenyl-3-methylbutene 
• 23586-64-3 (3,3-dimethylbut-1-ene-1,1-diyl)dibenzene 
• 1483-68-7 tetraphenylbutatriene 
• 134996-32-0 3,3-diphenyl-2-(phenylsulfonyl)-2-propenyl alcohol 
• 13112-46-4 2,2-diphenyl-1-phenylthioethene 
• 108365-51-1 (2,2-diphenylvinyl)(phenyl)selane 
• 768362-06-7 2-benzenesulfonyl-5-methyl-1,1-diphenylhexa-1,4-dien-3-one 
• 135204-17-0 3,3-diphenyl-2-(phenylsulfonyl)-2-propenyl chloroformate 
• 1460-13-5 (2-cyclopentylethene-1,1-diyl)dibenzene 

Relevant articles and documents

Synthesis of Sulfonated Benzo[d][1,3]oxazines by Merging Photoredox Catalysis and Insertion of Sulfur Dioxide

A photocatalytic reaction of N-(2-vinylphenyl)amides, DABCO?(SO2)2 and arenediazonium tetrafluoroborates for the synthesis of 4-((arylsulfonyl)methyl)-4H-benzo[d][1,3]oxazines under mild conditions is reported. This synthetic approac

Metal-Free Visible-Light Photocatalytic Tandem Radical Addition–Cyclization Strategy for the Synthesis of Sulfonyl-Containing Isoquinolinediones

A mild radical cascade reaction for the synthesis of sulfonyl-containing isoquinolinediones has been developed, in which sulfonyl radicals can be accessed from simple sodium sulfinates under visible light and eosin Y catalysis. This tandem approach features a broad range of substrates and functional group tolerance. With this strategy, trifluoromethylated isoquinolinedione was also obtained.

HUSY zeolite promoted hydrophenylation of alkynes conjugated with electron-withdrawing substituents

Arylacetylenes, conjugated with electron-withdrawing groups, ArC[tbnd6]C(EWG) [EWG = SO2Ph, PO(OEt)2, COMe, CO2Me] in reaction with benzene at room temperature or 130?°C (glass high pressure tube) for 1–10?h under the acti

Light-Mediated Difluoromethylthiolation of Aldehydes with a Hydrogen Atom Transfer Photocatalyst

A mild general method for difluoromethylthiolation of aldehydes with PhSO2SCF2H and a decatungstate photocatalyst under redox-neutral conditions has been developed. This reaction is highly efficient, scalable, and oxidant-free. The broad substrate scope and excellent functional group tolerance of the reaction make it suitable for generating libraries of difluoromethyl thioesters. We demonstrated the utility and sustainability of the method by synthesizing several structurally complex difluoromethyl thioesters.

Electrochemistry Enabled Nickel-Catalyzed Selective C?S Bond Coupling Reaction

This work describes an electrochemical enabled nickel-catalyzed chemoselective C?S bond coupling protocol for the production of aryl sulfides and sulfones. By simply switching the nickel catalysts and electrodes, this electrochemical C?S bond coupling has demonstrated excellent redox activity, scalability and sustainability. Furthermore, the mechanism for this electrochemical cross-coupling reaction has been investigated.

Visible-Light-Triggered Sulfonylation/Aryl Migration/Desulfonylation and C-S/Se Bond Formation Reaction: 1,2,4-Trifunctionalization of Butenyl Benzothiazole Sulfone with Thiosulfonate/Selenosulfonates

A visible-light-triggered radical cascade sulfonylation/aryl migration/desulfonylation and C-S/Se bond formation reaction of butenyl benzothiazole sulfone with thiosulfonates or selenosulfonates is developed. This study affords the 1,2,4-trifunctionalization of butenyl benzothiazole sulfone derivatives under mild conditions.