73062-38-1

Basic information

• Product Name: Benzene, 1,4-undecadienyl-, (E,E)-
• CAS NO: 73062-38-1
• Molecular Formula: C17H24
• Molecular Weight: 228.378
• Mol File: 73062-38-1.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Benzene, 1,4-undecadienyl-, (E,E)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1,4-undecadienyl-, (E,E)-(73062-38-1)
• EPA Substance Registry System: Benzene, 1,4-undecadienyl-, (E,E)-(73062-38-1)

Safety Data

• Hazardous Substances Data: 73062-38-1(Hazardous Substances Data)

Upstream product

• 35822-50-5 (Z)-methyl(styryl)sulfane 
• 7714-33-2 methyl phenylethynyl sulfide 
• 22433-33-6 Nona-1,2-dien 
• 37630-43-6 (Z)-1-(methylsulfonyl)-2-phenylethene 
• 4407-36-7 (2E)-3-phenyl-2-propen-1-ol 
• 853955-61-0 (E)-[2-(hydroxymethyl)phenyl]-dimethyl-(1-octenyl)-silane 
• 95932-32-4 tert-butyl (E)-cinnamyl carbonate 
• 118319-34-9 (E)-1-(dimethylfluorosilyl)-1-octene 
• 106625-69-8 ethyl (E)-3-phenyl-2-propenyl carbonate 
• 118319-47-4 difluoro(methyl)[(E)-1-octenyl]silane 

Relevant articles and documents

Regio- and stereoselective synthesis of 1,4-dienes

Titanocene(ii)-promoted cross-coupling between (Z)-alkenyl methyl sulfones and terminal allenes produced 1,4-dienes regioselectively via the formation of 2-alkylidenetitanacyclopentanes. Preferential formation of E,Z-dienes was observed in the reaction us

The Palladium-Catalyzed Cross-Coupling Reaction of Organosilicon Compounds with Allylic Carbonates or Diene Monoxides

The cross-coupling reaction of allylic carbonates with organosilanes was found to proceed without fluoride ion activation under mild conditions by using a coordinatively unsaturated palladium complex as a catalyst.The reaction was assumed to proceed through an allylpalladium alkoxide derived from the allylic carbonate substrate and a palladium(0) species, the alkoxo ligand activating the organosilicon reagent.Likewise, diene monoxides also underwent cross-coupling with alkenyl- and arylfluorosilanes in moderate to high yields.