55497-48-8

Upstream product

• 78-80-8 2-methylbut-1-en-3-yne 
• 2408-37-9 2,2,6-trimethylcyclohexan-1-one 
• 64547-54-2 1-(3-Methyl-but-3-en-1-ynyl)-2,2,6-trimethyl-cyclohexanol 

Downstream Products

• 855474-14-5 3-methyl-5-(2,6,6-trimethyl-cyclohex-1-enyl)-pent-2-en-4-ynal 
• 69037-26-9 1-[3-Methyl-3,5,5-trimethoxy-pent-1-yn-1-yl]-2,6,6-trimethylcyclohex-1-ene 
• 72834-86-7 6-methyl-8-(2,6,6-trimethyl-cyclohex-1-enyl)-octa-3,5-dien-7-yn-2-one 
• 72834-88-9 1-Chlor-3,7-dimethyl-9-(2,6,6-trimethyl-1-cyclohexenyl)-2,4,6-nonatrien-8-in 
• 72834-89-0 1-Brom-3,7-dimethyl-9-(2,6,6-trimethyl-1-cyclohexenyl)-2,4,6-nonatrien-8-in 
• 72834-87-8 1-[3,7-Dimethyl-nona-1-yne-3,5,8-trien-7-ol-1-yl]-2,6,6-trimethyl-cyclohex-1-ene 
• 69037-22-5 3,7-Dimethyl-9-(2,6,6-trimethyl-1-cyclohexenyl)-2,4,6-nonatrien-8-in-1-yl-acetat 
• 69037-27-0 1-[3-Methyl-3,5,5-triethoxy-pent-1-yn-1-yl]-2,6,6-trimethylcyclohex-1-ene 

Relevant academic research and scientific papers

Substituted 1-alkenynyl-cyclohexanols and -cyclohexenes and processes for their preparation

New substituted 1-alkenynyl-cyclohexanols and 1-alkenynyl-cyclohexenes. The 1-alkenynyl-cyclohexanols are obtained by reacting the corresponding cyclohexanone witn an enyne in the presence of a strongly basic condensing agent in an inert solvent, or with an alkali metal salt of an enyne in an inert solvent. The 1-alkenynyl-cyclohexenes are obtained by dehydrating the 1-alkenynyl-cyclohexanols or 1-cycloalkanolyl-alkynols. The new compounds are themselves interesting scents, but can also be used as starting materials for further interesting scents.