29747-19-1

Basic information

• Product Name: 7-hexadecynyl iodide
• Synonyms: 7-hexadecynyl iodide
• CAS NO: 29747-19-1
• Molecular Weight: 348.311
• Mol File: 29747-19-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 7-hexadecynyl iodide(CAS DataBase Reference)
• NIST Chemistry Reference: 7-hexadecynyl iodide(29747-19-1)
• EPA Substance Registry System: 7-hexadecynyl iodide(29747-19-1)

Safety Data

• Hazardous Substances Data: 29747-19-1(Hazardous Substances Data)

Upstream product

• 764-93-2 1-decyne 
• 629-09-4 1,6-diiodohexane 
• 34683-73-3 1-chloro-6-iodohexane 
• 1246077-93-9 7-hexadecynyl tosylate 

Downstream Products

• 7432-41-9 8(Z)-heptadecenoic acid 
• 1246078-13-6 (R)-11,19-octacosadiyne-1,3-diol 1-p-methoxybenzyl ether 
• 1246078-25-0 11,19-octacosadiyne-1,3-diol 1-p-methoxybenzyl ether 
• 1246078-24-9 (S)-11,19-octacosadiyne-1,3-diol 1-p-methoxybenzyl ether 

Relevant articles and documents

Pheromone synthesis. Part 244: Synthesis of the racemate and enantiomers of (11Z,19Z)-CH503 (3-acetoxy-11,19-octacosadien-1-ol), a new sex pheromone of male Drosophila melanogaster to show its (S)-isomer and racemate as bioactive

The enantiomers of (11Z,19Z)-3-acetoxy-11,19-octacosadien-1-ol were synthesized from the enantiomers of 3,4-epoxy-1-butanol PMB ether. Its racemate was also synthesized. Its (S)-isomer and racemate were shown to possess the same pheromone activity as CH503, a long-lived inhibitor of male courtship in Drosophila melanogaster, although the racemate was less active.