100606-74-4

Usage

Uses

Used in Perfumery and Flavor Industry:
(E)-NONA-2,8-DIEN-1-OL is used as a key ingredient in the production of perfumes and flavoring agents, capitalizing on its appealing floral and fruity scent to enhance the aroma of various products.
Used in Organic Synthesis:
(E)-NONA-2,8-DIEN-1-OL serves as a versatile precursor in organic synthesis, being utilized in the preparation of a wide range of chemicals and bioactive compounds, thus contributing to the development of new materials and pharmaceuticals.
Used in Plant Signaling and Defense:
(E)-NONA-2,8-DIEN-1-OL has been identified as a volatile component in certain plant species, playing a role in their signaling and defense mechanisms against environmental stressors and potential threats.

Upstream product

• 258341-24-1 non-8-en-2-yn-1-ol 
• 4117-10-6 6-hepten-1-ol 
• 17206-61-0 hept-6-enal 
• 158627-60-2 (E)-Nona-2,8-dienoic acid ethyl ester 

Downstream Products

• 1616868-99-5 (2S,4S,6R)-2-((S)-1-(benzyloxy)hept-6-enyl)-6-((2R,5R)-5-((R)-1-(benzyloxy)tridecyl)-tetrahydrofuran-2-yl)-tetrahydro-2H-pyran-4-ol 
• 1616868-85-9 (2S,6R)-2-((S)-1-(benzyloxy)hept-6-enyl)-6-((2R,5R)-5-((R)-1-(benzyloxy)tridecyl)-tetrahydrofuran-2-yl)-tetrahydro-2H-pyran 
• 1616868-89-3 (S)-2-((S)-1-(benzyloxy)hept-6-enyl)oxirane 
• 1616868-87-1 (4S,5S)-5-(benzyloxy)undeca-1,10-dien-4-ol 

Relevant academic research and scientific papers

Stereoselective synthesis of tetrahydropyran-tetrahydrofuran (THP-THF) core of (+)-muconin via Prins cyclization

A stereoselective synthesis of tetrahydropyran-tetrahydrofuran (THP-THF) core 2 of (+)-muconin (1) has been achieved using Prins cyclization as a key step to construct tetrahydropyran moiety. Other important transformations such as Wittig olefination, Sharpless epoxidation, regio-, and stereoselective exo-cyclization of the epoxy alcohol, titanocene induced regioselective deoxygenation of 2,3-epoxy alcohol, Grignard reaction, and Barton-McCombie reaction are successfully employed to accomplish the synthesis of THP-THF core 2.

ω-Ethylenic allylic substrates as alternatives to cyclic substrates in copper- and iridium-catalyzed asymmetric allylic alkylation

"Chemical Equation Presented" A new strategy to access highly enantioenriched cyclic compounds (up to 98%) Is proposed using ω-ethylenic allylic substrates through a one-pot asymmetric allylic alkylation and ring-closing metathesis. Such starting compounds can be seen as synthetic equivalents of cyclic allylic substrates.