39491-67-3

Basic information

• Product Name: Benzene, 1,3-octadienyl-, (Z,Z)-
• CAS NO: 39491-67-3
• Molecular Formula: C14H18
• Molecular Weight: 186.297
• Mol File: 39491-67-3.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: Benzene, 1,3-octadienyl-, (Z,Z)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1,3-octadienyl-, (Z,Z)-(39491-67-3)
• EPA Substance Registry System: Benzene, 1,3-octadienyl-, (Z,Z)-(39491-67-3)

Safety Data

• Hazardous Substances Data: 39491-67-3(Hazardous Substances Data)

Upstream product

• 100-42-5 styrene 
• 592-41-6 1-hexene 
• 188290-36-0 thiophene 
• 693-03-8 n-butyl magnesium bromide 
• 288-05-1 selenophene 
• 288-08-4 Tellurophen 
• 588-73-8 (Z)-β-bromostyrene 
• 187874-95-9 (Z)-1-hexenyldi(3-methyl-2-butyl)borane 
• 37490-22-5 2-[(E)-1-hexenyl]-1,3,2-benzodioxaborole 
• 588-72-7 [(E)-2-bromoethenyl]benzene 
• 693-02-7 hex-1-yne 

Downstream Products

• 1346745-35-4 1-phenyl-1,4-diacetoxy-2-octene 
• 1346745-33-2 1-phenyl-3,4-diacetoxy-1-octene 
• 1334604-35-1 C₁₈H₂₄O₄ 
• 1334604-36-2 C₁₈H₂₄O₄ 
• 1334604-33-9 C₁₈H₂₄O₄ 
• 1334604-34-0 C₁₈H₂₄O₄ 
• 1346745-34-3 1-phenyl-1,2-diacetoxy-3-octene 

Relevant articles and documents

Catalytic features of the reaction of oxidative cross-coupling of styrene and hexene-1

The reaction of oxidative cross-coupling of styrene and hexene-1 in the medium of ice acetic acid was studied in the presence of various active phases based on palladium deposited on carbon-containing carrying agents, activated carbon, fullerenes, astrale

Polymer-bound palladium-catalyzed cross-coupling of organoboron compounds with organic halides and organic triflates

The polymer-bound palladium-catalyzed cross-coupling reaction of electrophiles (i.e., halides and triflates) with oganoboron compounds to form carbon-carbon bonds was achieved at mild conditions with very high activity in the Suzuki coupling reaction. The polymeric catalyst can be easily separated from a reaction mixture and reused more than 10 times with no decrease in activity.

A Synthesis of Conjugated Dienes from Aromatic, Five-membered Heterocycles

Reactions of furan, thiophene, selenophene, and tellurophene as well as 2-methyl and 2,5-dimethyl derivatives of the first two heterocycles with phenyl-, methyl-, and n-butyl-magnesium bromides in the presence of ligated nickel dichloride are shown to yield buta-1,3-dienes mostly with retention of configuration.