340157-81-5

Basic information

• Product Name: 3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluoro-1-(4'-methylphenyl)dec-1-ene
• Synonyms: 3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluoro-1-(4'-methylphenyl)dec-1-ene
• CAS NO: 340157-81-5
• Molecular Weight: 536.231
• Mol File: 340157-81-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluoro-1-(4'-methylphenyl)dec-1-ene(CAS DataBase Reference)
• NIST Chemistry Reference: 3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluoro-1-(4'-methylphenyl)dec-1-ene(340157-81-5)
• EPA Substance Registry System: 3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluoro-1-(4'-methylphenyl)dec-1-ene(340157-81-5)

Safety Data

• Hazardous Substances Data: 340157-81-5(Hazardous Substances Data)

Upstream product

• 106-38-7 para-bromotoluene 
• 21652-58-4 1H,1H,2H-perfluorodecene 
• 624-31-7 4-tolyl iodide 

Relevant articles and documents

Efficient access to perfluoroalkylated aryl compounds by Heck reaction

Efficient introduction of perfluorinated tails onto aromatic rings has been achieved by Heck reaction between perfluoroalkenes and arenediazonium salts, catalysed by palladium acetate. Subsequent transition metal catalysed hydrogenation of the double bond afforded a large variety of aromatic compounds bearing an affinity for fluorous solvents. Formation of perfluoroalkylated phosphane ligands and their use in palladium-catalysed coupling between potassium trifluoro(vinyl)borates and diazonium salts is also described, allowing an easy separation and recycling of the catalytic system.