24022-76-2

Upstream product

• 95168-90-4 octadeca-11t,13t-dien-9-ynoic acid 
• 101887-86-9 octadeca-11t,13t-dien-9-ynenitrile 
• 96251-50-2 methyl (11E,13E)-11,13-octadecadien-9-ynoate 
• 96251-48-8 (E,E)-1-chloro-1,3-octadiene 
• 26076-75-5 (E)-hex-1-enyldiisobutylaluminum 
• 111699-12-8 13-t-butyl 1-methyl 3,4-tridecadiene-1,13-dioate 
• 111699-13-9 t-butyl (9Z,11E)-13-hydroxy-9,11-tridecadienoate 
• 111699-14-0 t-butyl (9Z,11E)-13-oxo-9,11-tridecadienoate 
• 111699-11-7 t-butyl 9-hydroxy-10-undecynoate 
• 111699-10-6 t-butyl 9-oxononanoate 
• 106369-41-9 1-methyl 13-t-butyl (2E,4Z)-2,4-tridecadiene-1,13-dioate 
• 16792-04-4 tert-butyl (9Z)-9-octadecenoate 
• 110-53-2 1-Bromopentane 
• 112-77-6 (Z)-9-octadecenoyl chloride 

Downstream Products

• 544-73-0 (9E,11E,13E)-9,11,13-octadecatrienoic acid 
• 71599-29-6 octadeca-9,11,13-trienoic acid ethyl ester 
• 505-48-6 octane-1,8-dioic acid 
• 107-92-6 butyric acid 
• 123-99-9 azelaic acid 
• 109-52-4 valeric acid 
• 131543-46-9 Glyoxal 
• 57-11-4 stearic acid 
• 822-10-6 (9Z,11E)-methyl octadeca-9,11-dienoate 

Relevant academic research and scientific papers

Stereoselective Synthesis of Octadeacpolyenoic Esters as an Insecticide

Octadecapolyenoic acid derivatives such as (+/-)-t-butyl coriolate, α-eleostearic acid, t-butyl punicate, and t-butyl (9Z,11E)-13-hydroxy-9,11-octadien-15-ynoate were synthesized starting from oleic acid with high stereoselectivity and their insecticidal

STEREOSELECTIVE PREPARATION OF 1-CHLORO-(E,E)-1,3-DIENES. APPLICATION TO THE SYNTHESIS OF METHYL ELEOSTEARATE.

The nickel (or palladium) catalyzed reaction of alkenylalanes with (E)-dichloroethylene affords 1-chloro-(E,E)-1,3-dienes under mild conditions.The syntheses of methyl α-eleostearate which is reported to be a feeding deterrent for the boll weevil on cotto