76238-22-7

Usage

Uses

Used in Perfumery and Fragrance Industry:
ACETIC ACID CIS-6-NONEN-1-YL ESTER is used as a fragrance ingredient for its ability to impart a fruity scent to perfumes, enhancing their overall appeal and attractiveness.
Used in Cosmetics Industry:
In the cosmetics industry, ACETIC ACID CIS-6-NONEN-1-YL ESTER is used as a flavoring agent and fragrance enhancer in products such as soaps, lotions, and creams. Its pleasant scent improves the sensory experience of using these products, making them more enjoyable for consumers.
Used in Food and Beverage Industry:
ACETIC ACID CIS-6-NONEN-1-YL ESTER is used as a flavoring agent in the food and beverage industry to add a fruity note to various products, enhancing their taste and aroma.
Used in Household Products Industry:
This chemical is used in the manufacturing of household products such as air fresheners and cleaning agents, where its pleasant scent helps to create a more enjoyable environment.
Used in Insect Management:
ACETIC ACID CIS-6-NONEN-1-YL ESTER is also used in the production of insect attractants and repellents, leveraging its properties to either lure or deter insects for pest control purposes.

Upstream product

• 87298-22-4 1-Tetrahydropyranyloxy-non-6(Z)-ene 
• 75-36-5 acetyl chloride 
• 119265-30-4 1,8-diacetoxy-2Z-octene 
• 74-88-4 methyl iodide 
• 60171-36-0 (Z)-Oct-2-ene-1,8-diol 
• 40709-05-5 (E/Z)-6-Nonen-1-ol 
• 87298-23-5 2-(trans-6,7-Epoxynonoxy)-tetrahydropyran 
• 55305-36-7 (E/Z)-2-(6-Nonenoxy)-tetrahydropyran 
• 68760-65-6 (6-hydroxyhexyl)triphenylphosphonium bromide 
• 31502-19-9 (Z)-6-nonenol 
• 108-24-7 acetic anhydride 

Downstream Products

• 143-13-5 nonyl acetate 
• 103109-24-6 9-hydroxyl nonanyl acetate 
• 616223-76-8 8-hydroxynonyl acetate 

Relevant academic research and scientific papers

Fe(PyTACN)-catalyzed cis-dihydroxylation of olefins with hydrogen peroxide

A family of iron complexes with general formula [Fe(II)( R,Y,XPyTACN)(CF3SO3)2], where R,Y,XPyTACN=1-[2′-(4-Y-6-X-pyridyl)methyl]-4,7-dialkyl-1,4, 7-triazacyclononane, X and Y refer to the groups at positions 4 and 6 of the pyridine, respectively, and R refers to the alkyl substitution at N-4 and N-7 of the triazacyclononane ring, are shown to be catalysts for efficient and selective alkene oxidation (epoxidation and cis-dihydroxylation) employing hydrogen peroxide as oxidant. Complex [Fe(II)(Me,Me,HPyTACN)(CF 3SO3)2] (7), was identified as the most efficient and selective cis-dihydroxylation catalyst among the family. The high activity of 7 allows the oxidation of alkenes to proceed rapidly (30 min) at room temperature and under conditions where the olefin is not used in large amounts but instead is the limiting reagent. In the presence of 3 mol% of 7, 2 equiv. of H2O2 as oxidant and 15 equiv. of water, in acetonitrile solution, alkenes are cis-dihydroxylated reaching yields that might be interesting for synthetic purposes. Competition experiments show that 7 exhibits preferential selectivity towards the oxidation of cis olefins over the trans analogues, and also affords better yields and high [syn-diol]/[epoxide] ratios when cis olefins are oxidized. For aliphatic substrates, reaction yields attained with the present system compare favourably with state of the art Fe-catalyzed cis-dihydroxylation systems, and it can be regarded as an attractive complement to the iron and manganese systems described recently and which show optimum activity against electron-deficient and aromatic olefins. Copyright

OZONOLYSIS OF ALKENES AND REACTIONS OF POLYFUNCTIONAL COMPOUNDS. XXXV. SYNTHESIS OF 8Z-DODECENYL- AND 11Z-TETRADECENYL ACETATES FROM THE CYCLIC DIMER OF BUTADIENE

The stereoselective synthesis of 8Z-dodecenyl- and 11Z-tetradecenyl acetates which are components of the sex pheromones of many species of insect of the order Lepidoptera, was realized on the basis of the partial ozonolysis of (Z,Z)-1,5-cyclooctadiene and its isomerization product (Z,Z)-1,3-cyclooctadiene.