30418-89-4

Usage

Uses

Used in Food Industry:
2-NONENYLACETATE is used as a flavoring agent for its fruity, orange-like odor, enhancing the taste and aroma of food products.
Used in Perfumery and Cosmetics Industry:
It serves as a fragrance component in perfumes and cosmetic products, adding a pleasant scent to these items.
Used in Air Freshener and Household Cleaning Products Industry:
2-NONENYLACETATE is utilized in the production of air fresheners and household cleaning products due to its appealing and refreshing scent, which helps to create a more pleasant environment.
Used in Insect Communication and Mating Behavior:
Recognized as a pheromone in certain insect species, 2-NONENYLACETATE plays a crucial role in their communication and mating processes.

InChI:InChI=1/C11H20O2/c1-3-4-5-6-7-8-9-10-13-11(2)12/h8-9H,3-7,10H2,1-2H3/b9-8+

Upstream product

• 76853-14-0 2-nonenyl bromide 
• 127-09-3 sodium acetate 
• 21964-44-3 non-1-en-3-ol 
• 3761-92-0 n-hexylmagnesium bromide 
• 1577-98-6 (E)-2-nonenoic acid 
• 31502-14-4 2-nonenyl alcohol 
• 108-24-7 acetic anhydride 
• 111-71-7 heptanal 
• 75-36-5 acetyl chloride 

Downstream Products

• 91434-08-1 3-chloronon-1-ene 
• 67242-74-4 (E)-1-chloro-2-nonene 
• 28665-57-8 (E)-2-methylundec-4-ene 

Relevant academic research and scientific papers

Titanocene-promoted eliminations on epoxy alcohols and epoxy esters

The reaction of a series of 2,3-epoxy alcohols and the corresponding formates, acetates, and benzoates promoted by Cp2TiCl has been studied. The different outcome of the reaction of epoxy derivatives has been rationalized in terms of mechanistically biased processes. After homolytic oxirane cleavage, four main types of reaction were found: dehydroxylation, decarboxylation, dehydrogenation, and deoxygenation. The reaction products varied according to the substitution pattern. The radical nature of these eliminations is demonstrated.

Oxidation of acetoxyalkyl radicals by divalent copper salts

1. The 1-ethyl-3-aeetoxypropyl and 1-ethyl-4-acetoxybutyl radicals were respectively generated by the oxidative decarboxylation of the 2-ethyl-3-acetoxybutanoic and 2-ethyl-4-acetoxypentanoic acids under the influence of lead tetraacetate, and a study was made of their oxidation by the acetate, trifluoroacetate, fluoborate, sulfate, chloride and perchlorate of divalent copper. 2. Most of the copper salts oxidize the 1-ethyl-3-acetoxypropyl and 1-ethyl-4-acetoxybutyl radicals exclusively to the 2- and 3-pentenyl and the 3- and 4-hexenyl acetates, with the predominant formation of the isomers where the acetoxy group is furthest away from the double bond. Ligands that are coordinated with the copper are practically without effect on the ratio of the formed isomeric alkenyl acetates.