61810-56-8

Basic information

• Product Name: (Z,E,Z)-trideca-4,7,10-trien-1-yl acetate
• Synonyms: (Z,E,Z)-trideca-4,7,10-trien-1-yl acetate;(3Z,6Z,9E)-13-Acetoxy-3,6,9-tridecatriene;(4E,7Z,10Z)-4,7,10-Tridecatrien-1-ol acetate;Acetic acid (4E,7Z,10Z)-4,7,10-tridecatrienyl ester
• CAS NO: 61810-56-8
• Molecular Formula: C₁₅H₂₄O₂
• Molecular Weight: 236.34986
• EINECS: 263-238-6
• Mol File: 61810-56-8.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 304.6°C at 760 mmHg
• Flash Point: 95.6°C
• Appearance: /
• Density: 0.907g/cm³
• Vapor Pressure: 0.000864mmHg at 25°C
• Refractive Index: 1.476
• CAS DataBase Reference: (Z,E,Z)-trideca-4,7,10-trien-1-yl acetate(CAS DataBase Reference)
• NIST Chemistry Reference: (Z,E,Z)-trideca-4,7,10-trien-1-yl acetate(61810-56-8)
• EPA Substance Registry System: (Z,E,Z)-trideca-4,7,10-trien-1-yl acetate(61810-56-8)

Safety Data

• Hazardous Substances Data: 61810-56-8(Hazardous Substances Data)

Usage

General Description

(Z,E,Z)-trideca-4,7,10-trien-1-yl acetate is a chemical compound with a complex molecular structure consisting of a trideca-4,7,10-trien-1-yl group attached to an acetate functional group. It is a type of acetate ester, which is commonly found in naturally occurring substances such as essential oils. This chemical compound is used in the production of fragrances and flavors, and it has a strong, sweet, and floral scent. It is also used in the manufacturing of cosmetics, perfumes, and various other consumer products. Additionally, (Z,E,Z)-trideca-4,7,10-trien-1-yl acetate has potential applications in the field of organic synthesis and chemical research due to its unique molecular structure and reactivity.

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

• 108-24-7 acetic anhydride 
• 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 
• 112182-99-7 2-(1-Vinyl-nona-3,6-diynyloxy)-tetrahydro-pyran 
• 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 
• 109384-86-3 ((2E,5Z,8Z)-2-Undeca-2,5,8-trienyl)-malonic acid diethyl ester 
• 109384-85-2 Carbonic acid methyl ester (2E,5Z,8Z)-undeca-2,5,8-trienyl ester 
• 101339-96-2 (2E,5Z,8Z)-2,5,8-undecatrien-1-ol 
• 35378-82-6 2,5,8-undecatriyne-1-ol 

Relevant articles and documents

Synthesis of (4E, 7Z, 10Z)-4,7,10-tridecatrein- 1-yl acetate

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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.