60714-17-2

Upstream product

• 40267-53-6 (E)-N,N-diethyl-3,7-dimethyl-2,6-octadienylamine 

Downstream Products

• 65094-68-0 (+/-)-5,5-dimethyl-1,2,3,4,5,6,7,8-octahydro-naphthalene-2r,3c-dicarboxylic acid-anhydride 
• 68991-96-8 5,5-dimethyl-1,2,3,4,5,6,7,8-octahydronaphthalene-2-carbaldehyde 
• 54345-56-1 (8,8-dimethyl-4-methylene)-1-oxaspiro<2.5>octane 
• 142453-17-6 7,7-dimethyl-1,5-dioxa-dispiro(2.0,2.4)decane 
• 56691-73-7 {[(2,6,6-trimethyl-1-cyclohexen-1-yl)methyl]thio}benzene 
• 186817-78-7 (2-Chloromethyl-6,6-dimethyl-cyclohex-1-enylmethylsulfanyl)-benzene 
• 157552-18-6 5-Hydroxy-3-oxo-5-(2,6,6-trimethyl-cyclohex-1-enyl)-pentanoic acid tert-butyl ester 
• 157552-26-6 1-Bromomethyl-2,3,3-trimethyl-cyclohexene 
• 157552-19-7 1,6,6,-trimethyl-2-methylenecyclohexan-1-ol 
• 127-41-3 alpha-ionone 
• 14505-74-9 α-cyclocitral 
• 79-77-6 (E)-β-ionone 
• 170240-86-5 iso-β-cyclogeranyl iodide 

Relevant academic research and scientific papers

Synthesis of (+/-)-Nanaimoal and (+/-)-Nanaimool from N,N-Diethylgeranylamine

(+/-)-Nanaimoal and (+/-)-nanaimool were synthesized via Diels-Alder Reaction of 1,1-dimethyl-2,3-dimethylenecyclohexane, a novel building block for cyclic terpenoids, easily prepared from N,N-diethylgeranylamine.

Cyclic terpenoid onium salts, their preparation and uses

Acyclic terpenoid onium salts are cyclized in an acidic aqueous solution at a temperature of at least about 80° C.