Home Chemistry Organic Building Blocks Alkenyls Cyclohexa-1,3-Diene
Electrophilic Addition Reactions: Cyclohexa-1,3-diene can undergo electrophilic addition reactions with electrophilic reagents. The conjugated double bonds make the diene more reactive than isolated double bonds.
Diels-Alder Reaction: Cyclohexa-1,3-diene is commonly used as a diene component in the Diels-Alder reaction. This reaction involves the cycloaddition of a diene and a dienophile (a compound with a double bond) to form a cyclic product.
Oxidation Reactions: It can undergo oxidation reactions, especially when subjected to powerful oxidizing agents. For instance, it can be oxidized to form cyclohexa-1,3-diene-1,5-diol.
Isomerization: In the presence of heat or catalysis, it can undergo isomerization reactions, such as 1,3-diene to 1,4-diene isomerization.
Polymerization: Under certain conditions, cyclohexa-1,3-diene can undergo polymerization to form various types of polymers.
Cycloaddition Reactions: It can participate in other cycloaddition reactions besides the Diels-Alder reaction, such as [2+2] cycloadditions.
Aromatization: Depending on reaction conditions and reagents, cyclohexa-1,3-diene can undergo reactions leading to the formation of aromatic compounds, like benzene derivatives.
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