1713-47-9

Basic information

• Product Name: 1,3-Cyclohexadiene, 2,3-diethenyl-
• CAS NO: 1713-47-9
• Molecular Formula: C10H12
• Molecular Weight: 132.205
• Mol File: 1713-47-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1,3-Cyclohexadiene, 2,3-diethenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-Cyclohexadiene, 2,3-diethenyl-(1713-47-9)
• EPA Substance Registry System: 1,3-Cyclohexadiene, 2,3-diethenyl-(1713-47-9)

Safety Data

• Hazardous Substances Data: 1713-47-9(Hazardous Substances Data)

Upstream product

• 6553-71-5 3,4-divinyl-1,3,5-hexatrien 
• 30154-99-5 meso-1,2,6,7-Cyclodecatetraen 

Relevant articles and documents

Computational and synthetic studies with tetravinylethylenes

Computational and experimental studies offer fresh insights into the neglected tetravinylethylene class of compounds. Both the structures and the outcomes of exploratory reactions of the parent hydrocarbon are predicted and explained in detail through hig

Tetravinylethylene

The first four-fold cross coupling reaction involving alkenic partners leads to the title hydrocarbon on multi-gram scale in one step from commercially available precursors. In stark contrast to its close structural relatives, tetravinylethylene is a remarkably robust, bench-stable compound. The π-bond rich hydrocarbon is shown to undergo one-pot sequences of pericyclic reactions leading to the formation of complex systems with four new rings, seven C-C bonds and ten stereocenters with a very high level of stereoselectivity. Insights into the reactivity of this and related systems is provided using the accurate composite ab initio MO G4(MP2) method. Targets very efficiently: The forgotten hydrocarbon, tetravinylethylene (TVE, scheme) is a bench-stable compound that can be synthesized in one step from commercially available starting materials. TVE is a vehicle for rapid complex molecule synthesis through one-pot sequences involving the stereoselective assembly of up to seven C-C bonds.