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(E,Z)-trideca-4,7-dien-1-yl acetate is a chemical compound characterized by a 14-carbon chain with double bonds at the 4th and 7th carbon positions, featuring an acetate functional group. This organic compound is known for its sweet and fruity aroma with a floral undertone, making it a valuable addition to the fragrance and flavor industry.

61389-12-6

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61389-12-6 Usage

Uses

Used in Fragrance and Flavor Industry:
(E,Z)-trideca-4,7-dien-1-yl acetate is used as a fragrance ingredient for its sweet and fruity aroma with a floral undertone. It is commonly incorporated into perfumes, colognes, and other scented products to enhance their overall scent profile and provide a pleasant, lasting impression on consumers.
Used in Insect Control:
In the agricultural industry, (E,Z)-trideca-4,7-dien-1-yl acetate is utilized as a pheromone in insect control strategies. It serves as a sex attractant for certain pest species, helping to manage and control their populations. By leveraging the natural chemical cues of insects, (E,Z)-trideca-4,7-dien-1-yl acetate contributes to more sustainable and environmentally friendly pest management practices.

Check Digit Verification of cas no

The CAS Registry Mumber 61389-12-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,3,8 and 9 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 61389-12:
(7*6)+(6*1)+(5*3)+(4*8)+(3*9)+(2*1)+(1*2)=126
126 % 10 = 6
So 61389-12-6 is a valid CAS Registry Number.
InChI:InChI=1/C15H26O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-17-15(2)16/h7-8,10-11H,3-6,9,12-14H2,1-2H3/b8-7-,11-10+

61389-12-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name [(4E,7Z)-trideca-4,7-dienyl] acetate

1.2 Other means of identification

Product number -
Other names EINECS 262-757-5

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:61389-12-6 SDS

61389-12-6Downstream Products

61389-12-6Relevant academic research and scientific papers

Exo- and endohormones XXI 1: Stereoselective synthesis of the four isomers of the 4,7-tridecadien-1-yl acetate. (4E,7Z)-4,7-tridecadien-1-yl acetate, the sex pheromone of the leafminer moth Phylonorycter corylifoliella

Ganscǎ, Lucia,Gocan, Alexandra,Oprean, Ioan,Maxim, Sanda,Budae, Iuliana

, p. 1243 - 1248 (2007/10/03)

The synthesis of the four isomers of 4,7-tridecadien-1-yl acetate, based on a C5+C8 scheme is described. The coupling reaction took place between the Grignard reagent of pent-4-yn-1-oic acid and 1-bromo-2(Z/E)-octene. The four isomers were separated on SiO2-AgNO3 TLC plate and GS-MS. (4E,7Z)-4,7-Tridecadien-1-yl acetate is the sex pheromone of the spottet tentiform leafminer moth Phylonorycter corylifoliella.

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

Ishchenko, R. I.,Kovalev, B. G.

, p. 258 - 262 (2007/10/02)

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.

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