20130-95-4

Basic information

• Product Name: (4E)-hexa-1,2,4-triene
• Synonyms: (E)-1,2,4-Hexatriene; 1,2,4-Hexatriene, (E)-
• CAS NO: 20130-95-4
• Molecular Formula: C₆H₈
• Molecular Weight: 80.1277
• Mol File: 20130-95-4.mol

Chemical Properties

• Boiling Point: 87°C at 760 mmHg
• Density: 0.697g/cm³
• Vapor Pressure: 73.1mmHg at 25°C
• Refractive Index: 1.428
• CAS DataBase Reference: (4E)-hexa-1,2,4-triene(CAS DataBase Reference)
• NIST Chemistry Reference: (4E)-hexa-1,2,4-triene(20130-95-4)
• EPA Substance Registry System: (4E)-hexa-1,2,4-triene(20130-95-4)

Safety Data

• Hazardous Substances Data: 20130-95-4(Hazardous Substances Data)

Upstream product

• 2983-25-7 1,2-dibromopropyl ethyl ether 
• 106-96-7 propargyl bromide 
• 61823-76-5 1,1-dibromo-2-(E-propenyl)cyclopropane 
• 124-41-4 sodium methylate 
• 99779-59-6 C₇H₁₁N₃O₂ 

Relevant articles and documents

THE DIAZO ROUTE TO 2-VINYLCYCLOPROPYLIDENES

2-Vinylcyclopropylidene (2), 3-methyl-2-vinylcyclopropylidenes (79,80) and 2-(1-propenyl)cyclopropylidenes (95,97) were generated from the corresponding nitrosoureas in methanol at room temperature.The diazo route is initiated by the formation of 2-vinylcyclopropanediazonium ions (e.g. 43) which do not undergo 1,3-carbon shifts.No cyclopentenyl products were found in weakly basic methanol where the diazonium ions prevail.Ring opening of the diazonium ions gives pentadienyl cations and products derived therefrom.Delocalisation of the pentadienyl cations was demonstrated by the distribution of deuterium and methyl labels.In the presence of strong base, 1-diazo-2-vinylcyclopropanes (e.g. 48) arise by deprotonation of the diazonium ions.Rearrangement of 48 was excluded by independent generation of the potential product, 4-diazocyclopentene (103).Substantial quantities of 3-methoxycyclopentene (108) were obtained from 103, but not from 48.The 2-vinylcyclopropylidenes 2, 79 and 95, arising by loss of nitrogen from the corresponding diazo compounds, undergo allene formation and Skatteboel rearrangement competitively.Cis-oriented methyl groups at either C-2 (81) or C-2' (97) prevent the Skattebol rearrangement.The cyclopentenylidenes 3 and 83 yield 4-methoxycyclopentes (52,86) in excess over cyclopentadiens (4,84).In the presence of methyl vinyl ether, cycloaddition of 3 and electrophilic addition of 3-cyclopentenyl cation (51) occured in a 1:14 ratio.Stereospecific formation of 52 indicates protonation of a 'foiled carbene' (3a) to give a bishomocyclopropenyl ion (51a).Our studies confirm that the various routes to 2-vinylcyclopropylidenes converge at the carbene stage.

Chemistry of gem-Dihalocyclopropanes. XX. The Effect of Methyl and Phenyl Substituents on the Vinylcyclopropylidene-Cyclopentenylidene Rearrangement

Reactions of gem-dibromocyclopropanes of the general structure 1 with methyllithium have been studied.In the most cases cyclopentadienes and/or vinylallenes are the products formed.The results obtained give evidence of a profound substituent effect on the carbene-carbene rearrangement leading to cyclopentadienes.We believe the effect is essentially steric in origin.The results support the mechanism proposed for the rearrangement.