1512864-83-3

Basic information

• Product Name: (E)-1-methyl-4-((4-(trifluoromethyl)styryl)sulfonyl)benzene
• Synonyms: (E)-1-methyl-4-((4-(trifluoromethyl)styryl)sulfonyl)benzene
• CAS NO: 1512864-83-3
• Molecular Weight: 326.339
• Mol File: 1512864-83-3.mol
• Article Data: 11

Chemical Properties

• CAS DataBase Reference: (E)-1-methyl-4-((4-(trifluoromethyl)styryl)sulfonyl)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-1-methyl-4-((4-(trifluoromethyl)styryl)sulfonyl)benzene(1512864-83-3)
• EPA Substance Registry System: (E)-1-methyl-4-((4-(trifluoromethyl)styryl)sulfonyl)benzene(1512864-83-3)

Safety Data

• Hazardous Substances Data: 1512864-83-3(Hazardous Substances Data)

Upstream product

• 402-50-6 1-trifluoromethyl-4-vinyl-benzene 
• 98-59-9 p-toluenesulfonyl chloride 
• 101973-46-0 diethyl ((p-tolylthio)methyl)phosphonate 
• 106-45-6 para-thiocresol 
• 455-19-6 4-Trifluoromethylbenzaldehyde 
• 60682-95-3 1-(diethoxyphosphorylmethylsulfonyl)-4-methylbenzene 
• 824-79-3 sodium 4-methylbenzenesulfinate 
• 1059140-27-0 1-(2-bromovinyl)-4-(trifluoromethyl)benzene 
• 2062-26-2 3-<4'-(trifluoromethyl)phenyl>-2-propenoic acid 
• 1576-35-8 toluene-4-sulfonic acid hydrazide 
• 123077-46-3 4-methyl-N'-(1-(4-(trifluoromethyl)phenyl)ethylidene)benzenesulfonohydrazide 
• 16642-92-5 4-(trifluoromethyl)cinnamic acid 
• 3792-88-9 3-[4-(trifluoromethyl)phenyl]-2-propynoic acid 

Relevant articles and documents

Copper-Catalyzed Heck-Type Couplings of Sulfonyl Chlorides with Olefins: Efficient and Rapid Access to Vinyl Sulfones

A copper-catalyzed redox-neutral alkene sulfonylation reaction has been developed. This reported protocol can be easily scale up to a gram scale, and smoothly applied to the late-stage modification of several bioactive molecules.

Electrochemical Synthesis of Vinyl Sulfones by Sulfonylation of Styrenes with a Catalytic Amount of Potassium Iodide

An electrochemical sulfonylation reaction of styrenes was developed in which sodium arylsulfinates were used as sulfonylating reagents, a catalytic amount of KI was used as a redox mediator, and Bu 4NBF 4was used as the electrolyte. In addition to various styrenes, sodium arylsulfinates with either electron-donating or electron-withdrawing groups were tolerated.

Electron Donor-Acceptor Complex Enabled Decarboxylative Sulfonylation of Cinnamic Acids under Visible-Light Irradiation

Visible-light-induced decarboxylative sulfonylation of cinnamic acids with aryl sulfonate phenol esters enabled by the electron donor-acceptor complex is developed. The method offers a mild and green approach for the synthesis of vinyl sulfones with excellent functional group compatibility under photocatalyst and oxidant-free conditions.