56599-51-0

Upstream product

• 917-64-6 methyl magnesium iodide 
• 629-80-1 n-hexadecylaldehyde 
• 108-05-4 vinyl acetate 
• 16813-18-6 2-heptadecanol 
• 110046-51-0 hept-6-en-1-yl 4-methylbenzenesulfonate 
• 107175-49-5 6-hepten-1-yl iodide 
• 4117-10-6 6-hepten-1-ol 
• 1176914-11-6 (2R,8Z)-8-heptadecen-2-ol 
• 108-24-7 acetic anhydride 
• 1392275-21-6 (R)-8-heptadecyn-2-ol 
• 1392275-22-7 (S)-1,2-epoxy-8-heptadecyne 
• 1392275-20-5 (+/-)-1,2-epoxy-8-heptadecyne 
• 1392275-19-2 1-heptadecen-8-yne 
• 764-93-2 1-decyne 

Relevant academic research and scientific papers

Synthesis of (1R,7Z)-1-methyl-7-hexadecenyl acetate, the female sex pheromone of the honey locust gall midge

(1R,7Z)-1-Methyl-7-hexadecenyl acetate (1), the female sex pheromone of the honey locust gall midge (Dasineura gleditchiae), was synthesized from 6-hepten-1-ol in an 8.9% overall yield (eight steps). Hydrolytic kinetic resolution of (±)-1,2-epoxy-8-heptad

Studies on PPL catalyzed acetylation of 2-alkanols: Its application for the synthesis of 2-dodecanol and 2-tridecyl acetate, the pheromones of Crematogaster ants and Drosophila mulleri flies

Several aliphatic 2-alkanols with varying chain length has been efficiently resolved by their acetylation using vinyl acetate/PPL in diisopropyl ether. The effect of solvent polarity, position and type of unsaturation and chain length has been probed. This has led to more convenient synthesis of some insect pheromones.