59841-29-1

Upstream product

• 2270-59-9 1-bromo-4-methylpent-3-ene 
• 69253-50-5 Diethyl-[2-(5-methyl-cyclohexa-1,4-dienyloxy)-ethyl]-amine 
• 487-51-4 4-carbethoxy-3-methyl-2-cyclohexen-1-one 
• 59841-28-0 2-Methyl-3-(4-methyl-pent-3-enyl)-4-oxo-cyclohex-2-enecarboxylic acid ethyl ester 

Downstream Products

• 73583-16-1 1,3-Dimethyl-2-(4-methyl-pent-3-enyl)-cyclohex-2-enol 
• 75596-77-9 1-<1-Hydroxy-3-methyl-2-(4-methylpent-3-enyl)cyclohex-2-enyl>-4,7-octandion-bis(ethylenacetal) 
• 98361-53-6 C₂₀H₂₄⁽²⁾HNO₄ 
• 90740-18-4 2-(4-methyl-3-pentenyl)-3-methyl-2-cyclohexenyl p-nitrobenzoate 
• 98361-50-3 C₁₃H₂₁⁽²⁾HO 
• 98361-38-7 3-Methyl-2-(4-methyl-pent-3-enyl)-cyclohex-2-enol 

Relevant academic research and scientific papers

Solvolysis of 2-Alkenyl-2-cyclohexenyl p-Nitrobenzoates

In an attempt to study possible ?-participation in allyl derivatives, 2-alkenyl-3-methyl-2-cyclohexenyl p-nitrobenzoates 6 and 7 were solvolyzed in 97 wt percent trifluoroethanol and 80 vol percent ethanol.These esters show in both solvents a solvolysis r

3-Methylcyclohex-2-enone Derivatives as Initiators of Cyclisation. Part 1. Introduction and Synthesis of 2-Substituted 3-methylcyclohex-2-enones

A series of C-2 substituted 3-methylcyclohex-2-enones has been prepared using the Hagemann ester route.A new synthesis of these compounds has been developed which involves the alkylation of the N,N-diethylaminoethyl ether of 1-hydroxy-5-methylcyclohexa-1,5-diene.The cyclohexenones have been converted into the corresponding α,β-epoxyketones using alkaline hydrogen peroxide.