72349-94-1

Upstream product

• 3196-23-4 methyl 1-bromocyclohexanecarboxylate 
• 123-38-6 propionaldehyde 

Downstream Products

• 72349-95-2 1-Isopropenylcyclohexancarbonsaeure-methylester 
• 116927-42-5 (E)-1-Isopropenyl-1-(1-propenyl)cyclohexan 
• 116927-20-9 (Z)-1-Isopropenyl-1-(1-propenyl)cyclohexan 
• 116927-17-4 1-Isopropenylcyclohexancarbaldehyd 
• 116927-15-2 1-Isopropenylcyclohexanmethanol 
• 116927-21-0 1-Isopropenyl-1-(2-methyl-1-propenyl)cyclohexan 
• 116927-19-6 1-Ethenyl-1-isopropenylcyclohexan 

Relevant academic research and scientific papers

Hydrocarbonylating Cyclization of Dienes, 6. - Metal-Induced Skeletal Rearrangements during an Attempted Synthesis of the Acorane System from Substituted 1,1-Divinylcyclohexanes

In attempts of a regio- and stereoselective synthesis of the acorane skeleton 2, substituted 1,1-divinylcyclohexanes 1 were treated under the conditions of hydrocarbonylating cyclization.Substrates with higher degree of substitution surprisingly did not l

Pharmaceutically active cyclohexyl compounds and their preparation

The chemical compounds of the invention are useful as the active compound in drugs because of their anticonvulsant and/or antianoxic activity. They have the general formula STR1 wherein Z is a hydroxyl group; a group--OM wherein M is an alkali metal atom or an equivalent atom fraction of an alkaline-earth metal or an amino group such as --NH2, and R is a linear or branched alkyl group containing from 1 to 9 carbon atoms, and optionally substituted by one or more halogen atoms; a linear or branched alkenyl or alkynyl, alkoxyalkyl, or acylalkyl group containing from 2 to 9 carbon atoms and optionally substituted by one or more halogen atoms; an aryl or arylalkyl or aryloxyalkyl group comprising at least one aromatic radical and an alkyl chain having from 1 to 4 carbon atoms.