80959-78-0

Basic information

• Product Name: 1-Methyl-4-((E)-3,3,3-trifluoro-propenyl)-benzene
• Synonyms: 1-Methyl-4-((E)-3,3,3-trifluoro-propenyl)-benzene
• CAS NO: 80959-78-0
• Molecular Weight: 186.177
• Mol File: 80959-78-0.mol
• Article Data: 31

Chemical Properties

• CAS DataBase Reference: 1-Methyl-4-((E)-3,3,3-trifluoro-propenyl)-benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Methyl-4-((E)-3,3,3-trifluoro-propenyl)-benzene(80959-78-0)
• EPA Substance Registry System: 1-Methyl-4-((E)-3,3,3-trifluoro-propenyl)-benzene(80959-78-0)

Safety Data

• Hazardous Substances Data: 80959-78-0(Hazardous Substances Data)

Upstream product

• 75-63-8 Bromotrifluoromethane 
• 60655-80-3 (E)-4-methylstyrenyl bromide 
• 677-21-4 1,1,1-trifluoropropylene 
• 624-31-7 4-tolyl iodide 
• 887144-94-7 Togni's reagent II 
• 1192488-87-1 (Z)-2-(2-(4-methylphenyl)vinyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 622-97-9 1-ethenyl-4-methylbenzene 
• 421-83-0 trifluoromethane sulfonyl chloride 
• 2314-97-8 iodotrifluoromethane 
• 73839-44-8 (Z)-1-[2-bromovinyl]-4-methylbenzene 
• 1866-39-3 4-methylcinnamic acid 
• 460-37-7 1,1,1-trifluoro-3-iodopropane 
• 75-90-1 2,2,2-Trifluoroacetaldehyde 
• 104-81-4 4-Methylbenzyl bromide 

Relevant articles and documents

Exploring the Structure and Performance of Cd–Chalcogenide Photocatalysts in Selective Trifluoromethylation

The field of heterogeneous photoredox catalysis has grown substantially and impacted organic synthesis because of the affordability and reusability of catalysts. This study reports radical trifluoromethylation with Cd–chalcogenide semiconductors. Cd semiconductors, particularly CdSe, are readily available, commercial, visible-light-responsive, heterogeneous photocatalysts. The potential of readily available Cd semiconductors, particularly CdSe, is confirmed by their increased photocatalytic activity toward trifluoromethylation with various substrates, such as (hetero)arenes and vinylic amides/acids, via addition, cyclization, and decarboxylation under visible light. The economic significance of this strategy is also highlighted through the scalable synthesis of biologically active molecules followed by catalyst reuse. Moreover, these catalysts are relatively inexpensive compared with transition metal-based homogeneous photocatalysts, presently used in organic synthesis.

Merging hypervalent iodine and sulfoximine chemistry: A new electrophilic trifluoromethylation reagent

Electrophilic trifluoromethylation is at the forefront of methodologies available for the installation of the CF3 moiety to organic molecules; research in this field is largely spurred by the availability of stable and accessible trifluoromethy

Electrochemical Decarboxylative Trifluoromethylation of α, β-Unsaturated Carboxylic Acids with CF3SO2Na

A new method for the synthesis of vinyl trifluoromethyl compounds from α, β-unsaturated carboxylic acids and CF3SO2Na has been developed. This electrochemical decarboxylative trifluoro-methylation was found to be highly stereoselective and afforded products in good yields with wide substrate scope under metal-free and external chemical oxidant-free conditions.