61810-56-8

Usage

Uses

Used in Fragrance and Flavor Industry:
(Z,E,Z)-trideca-4,7,10-trien-1-yl acetate is used as a key ingredient in the production of fragrances and flavors due to its distinctive and appealing aroma. Its strong, sweet, and floral scent makes it a valuable addition to a variety of products in this industry.
Used in Cosmetics and Perfumery:
In the cosmetics and perfumery industry, (Z,E,Z)-trideca-4,7,10-trien-1-yl acetate is utilized as a fragrance component to enhance the scent profiles of various cosmetic products, including perfumes, lotions, and creams. Its unique scent contributes to the overall sensory experience of these products.
Used in Consumer Product Manufacturing:
(Z,E,Z)-trideca-4,7,10-trien-1-yl acetate is also used in the manufacturing of a wide range of consumer products, where its scent can be incorporated to provide a pleasant olfactory experience for the end-user.
Used in Organic Synthesis and Chemical Research:
Due to its unique molecular structure and reactivity, (Z,E,Z)-trideca-4,7,10-trien-1-yl acetate has potential applications in the field of organic synthesis and chemical research. Researchers may explore its properties and reactions to develop new compounds and materials with various applications.

InChI:InChI=1/C15H24O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-17-15(2)16/h4-5,7-8,10-11H,3,6,9,12-14H2,1-2H3/b5-4+,8-7+,11-10+

Upstream product

• 111285-96-2 (4E,7Z,10Z)-4,7,10-tridecatrien-1-ol 
• 75-36-5 acetyl chloride 
• 128461-73-4 1-tetrahydropyranyloxy-(4E,7Z,10Z)-4,7,10-tridecatriene 
• 105894-11-9 1-bromo-(2Z,5Z)-2,5-octadiene 
• 35378-82-6 2,5,8-undecatriyne-1-ol 
• 112182-99-7 2-(1-Vinyl-nona-3,6-diynyloxy)-tetrahydro-pyran 
• 101339-95-1 (5Z,8Z)-5,8-undecadien-2-yn-1-ol 
• 128461-72-3 1-bromo-(2E,5Z,8Z)-2,5,8-undecatriene 
• 35389-48-1 (5Z,8Z)-(+/-)-1,5,8-undecatrien-3-ol 
• 112183-01-4 2-((3Z,6Z)-1-Vinyl-nona-3,6-dienyloxy)-tetrahydro-pyran 
• 111285-94-0 ethyl 7,10-tridecadiyn-4(E)-enoate 
• 111285-95-1 ethyl (4E,7Z,10Z)-4,7,10-tridecatrienoate 
• 81717-80-8 5,8-undecadiyn-1-en-3-ol 
• 1573-66-6 hex-1-en-5-yn-3-ol 

Relevant academic research and scientific papers

SYNTHETIC INVESTIGATIONS IN THE FIELD OF INSECT ATTRACTANTS (SEX ATTRACTANTS). II. SYNTHESIS OF FOUR ISOMERS OF 4,7-TRIDECADIENYL ACETATE AND (E,Z,Z)-4,7,10-TRIDECATRIENYL ACETATE

A common approach was developed to the synthesis of (E,Z)-4,7-tridecadienyl and (E,Z,Z)-4,7,10-tridecatrienyl acetates, which are the main components of the sex pheromone of the female potato moth Phtorimaea operculella, on the basis of 4-pentyn-1-ol and allyl halides.The Z,Z, Z,E, and E,E isomers of 4,7-tridecadienyl acetate were also obtained by the method.

Synthesis of Pheromones of Potato Tuberworm Moth, Phthorimaea opericulella (Zeller)

The alcohol (3) having highly flexible dual functionality (terminal acetylene and a terminal double bond), has been utilised for the synthesis of (n,n+3) alkadienes.The simplicity of this procedure has been illustrated by the synthesis of potato tuberworm moth pheromones, PTM-1 (1a) and PTM-2 (1b).

A NEW STEREOSELECTIVE SYNTHESIS OF (E,Z,Z)-4,7,10-TRIDECATRIEN-1-OL ACETATE, COMPONENT OF THE SEX PHEROMONE OF Phthorimaea operculella

The synthesis of (E,Z,Z)-2,5,8-undecatrien-1-ol 3 and its conversion to (E,Z,Z)-4,7,10-tridecatrien-1-ol acetate II is reported.The synthetic route disclosed is relatively easy and could be applied to produce other trienic compounds.

Synthesis of (4E,7Z)-4,7-Tridecadienyl Acetate and (4E,7Z,10Z)-4,7,10-Tridecatrienyl Acetate - The Sex Pheromones of Potato Tuberworm Moth

(4E,7Z)-4,7-Tridecadienyl acetate (1) and (4E,7Z,10Z)-4,7,10-tridecatrienyl acetate (2), the sex pheromones of potato tuberworm moth have been synthesized from a common intermediate 1-hexen-5-yn-3-ol (3) employing Claisen rearrangement as a key step to generate the trans-double bond.