65954-19-0

Usage

Uses

Used in Fragrance and Flavor Industry:
Z-4-TRIDECEN-1-YL ACETATE is used as a synthetic aroma compound for its ability to enhance the olfactory profile of various consumer goods. It is valued for its compatibility with a wide range of other ingredients, making it a popular choice in the creation of perfumes, soaps, and air fresheners.
Used in Perfumes:
Z-4-TRIDECEN-1-YL ACETATE is used as a fragrance ingredient to provide a fruity scent, contributing to the overall aroma of perfumes and ensuring a pleasant and appealing smell.
Used in Soaps:
In the soap industry, Z-4-TRIDECEN-1-YL ACETATE is used as a scent enhancer to impart a fresh and fruity fragrance to soap products, improving the sensory experience for consumers.
Used in Air Fresheners:
Z-4-TRIDECEN-1-YL ACETATE is utilized as a key component in air fresheners to deliver a natural and fruity scent, effectively masking unwanted odors and creating a more pleasant environment.
Regulatory Approval:
Z-4-TRIDECEN-1-YL ACETATE is considered safe for use in fragrance and flavor applications and has been approved by regulatory bodies for its inclusion in these formulations, ensuring consumer safety and product compliance.

InChI:InChI=1/C15H28O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-17-15(2)16/h10-11H,3-9,12-14H2,1-2H3/b11-10-

Upstream product

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• 35329-59-0 tridec-4E-enoic acid 
• 129908-61-8 tridec-5Z-en-4-olide 
• 129908-60-7 tridec-5-en-4-olide 
• 84200-37-3 (E)-diethyl (but-2-en-1-yl)malonate 
• 1426946-85-1 ethyl (4E)-5-chloropent-4-enoate 

Relevant academic research and scientific papers

Fe-catalyzed synthesis of (4E)-tridec-4-en-1-yl acetate, sex pheromone of tomato pinworm (Keiferia lycopersicella)

Starting with industrially available 1,3-dichloropropene a stereoselective process was developed for the preparation of (4E)-tridec-4-en-1-yl acetate, sex pheromone of tomato pinworm (Keiferia lycopersicella) using in the key stage the Fe-catalyzed cross-coupling of ethyl (4E)-5-chloropent-4-enoate with octylmagnesium bromide.

LOW-MOLECULAR-MASS BIOREGULATORS. III. SYNTHESIS OF TRIDEC-4E-ENYL ACETATE-THE SEX PHEROMONE OF Keiferia lycopersicella

A new method has been developed for the synthesis of tridec-4E-enyl acetate - the sex pheromone of the tomato pinworm Keiferia lycopersicella.

ALKYLATION OF ACETYLCYCLOPROPANE CYCLOHEXYLIMINE BY ETHYLENE OXIDE DERIVATIVES AS A KEY STEP IN THE SYNTHESIS OF SOME INSECT ACETOGENIN PHEROMONES

The interaction of Li derivatives of acetylcyclopropane cyclohexylimine with ethylene, propylene, and isoprene oxides leads efficiently to the corresponding γ-cyclopropylketols.The cyclopropylcarbinol corresponding to the first of them is smoothly converted under the action of the couple Me3SiBr/ZnBr2 to a linear E-C7-homoallyl bromide, which is then used in the stereocontrolled synthesis of tridec-4E-enyl and trideca-4E,7Z-dienyl acetates - components of the sex pheromones of some Lepidoptera species.Keywords: acetylcyclopropane, insect acetogenin pheromones, homoallyl rearrangement, Julia olefination, olefin oxides.

Acetylcyclopropane as a Five-Carbon Building Block in the Synthesis of some Acetogenin Insect Pheromones

Interaction of deprotonated acetylcyclopropane cyclohexylimine with several aliphatic alkyl halides, epoxides, and aldehydes efficiently gave the corresponding cyclopropyl ketones.Some of the respectible alcohols were rearranged in a highly stereoselective manner under the action of trimethylsilyl bromide in the presence of zinc bromide into the corresponding linear (E)-homoallyl bromides.The latter were used, in turn, as key intermediates in concise syntheses of thirteen terminally functionalized straight-chain oligoolefins which are known to constitute acetogenin pheromonal components for more than 65 species of lepidopteran insects.