87242-10-2

Upstream product

• 87242-02-2 11-(tetrahydro-2H-pyran-2-yloxy)undec-2-yn-1-ol 
• 87242-07-7 2-((Z)-11-Benzenesulfonyl-undec-9-enyloxy)-tetrahydro-pyran 
• 87242-06-6 2-((Z)-11-Chloro-undec-9-enyloxy)-tetrahydro-pyran 
• 87242-05-5 (Z)-11-(Tetrahydro-pyran-2-yloxy)-undec-2-en-1-ol 
• 50816-19-8 8-bromooctanol 
• 629-41-4 1,8-Octanediol 
• 50816-20-1 2-(8-bromooctyloxy)tetrahydropyran 
• 18162-48-6 tert-butyldimethylsilyl chloride 
• 87242-09-9 (Z)-11-Benzenesulfonyl-undec-9-en-1-ol 

Downstream Products

• 51760-35-1 (Z)-9,11-dodecadienyl acetate 

Relevant academic research and scientific papers

Stereoselective Syntheses of E- and Z-9,11-Dodecadien-1-yl Acetates: The Major Sex Pheromones of the Red Bollworm Moth

The sex pheromones 1 and 2 of the red bollworm moth were synthesized in a highly stereoselective manner.The key step of their syntheses was the olefination reaction of E- and Z-allyl phenyl sulfones 8 and 12, affording the corresponding dienes 9 and 15, respectively.Keywords - E-9,11-dodecadien-1-yl acetate; Z-9,11-dodecadien-1-yl acetate; sex pheromone; red bollworm moth; allyl sulfone; tri-n-butylstannylmethyl iodide