54664-97-0

Basic information

• Product Name: (Z,Z)-tetradeca-9,11-dienyl acetate
• Synonyms: (Z,Z)-tetradeca-9,11-dienyl acetate;(E,Z)-9,11-Tetradecadienyl acetate;(9Z,11Z)-9,11-Tetradecadien-1-yl acetate;9,11-Tetradecadien-1-ol, 1-acetate, (9Z,11Z)-;9,11-Tetradecadien-1-ol, acetate, (9Z,11Z)-;Einecs 259-286-2
• CAS NO: 54664-97-0
• Molecular Formula: C₁₆H₂₈O₂
• Molecular Weight: 252.39232
• EINECS: 259-286-2
• Mol File: 54664-97-0.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 378°C at 760 mmHg
• Flash Point: 107.1°C
• Appearance: /
• Density: 0.89g/cm³
• Vapor Pressure: 6.47E-06mmHg at 25°C
• Refractive Index: 1.463
• CAS DataBase Reference: (Z,Z)-tetradeca-9,11-dienyl acetate(CAS DataBase Reference)
• NIST Chemistry Reference: (Z,Z)-tetradeca-9,11-dienyl acetate(54664-97-0)
• EPA Substance Registry System: (Z,Z)-tetradeca-9,11-dienyl acetate(54664-97-0)

Safety Data

• Hazardous Substances Data: 54664-97-0(Hazardous Substances Data)

Usage

Description

(Z,Z)-tetradeca-9,11-dienyl acetate is a chemical compound characterized by a long carbon chain with double bonds at the 9th and 11th carbon atoms, and an acetate functional group. It is predominantly found in the pheromones of insects, playing a crucial role in their communication and mating behavior.

Uses

Used in Pest Control:
(Z,Z)-tetradeca-9,11-dienyl acetate is used as a pheromone in the pest control industry to control insect populations. By disrupting the mating behavior of insects, it helps in managing and reducing their numbers, making it an effective tool for pest management.
Used in Fragrance and Flavor Industry:
(Z,Z)-tetradeca-9,11-dienyl acetate is used as a key ingredient in the fragrance and flavor industry due to its sweet, floral, and fruity aroma. It is commonly utilized in the formulation of perfumes and aromatherapy products, adding a pleasant and attractive scent to these products.

InChI:InChI=1/C16H28O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-18-16(2)17/h4-7H,3,8-15H2,1-2H3/b5-4-,7-6-

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Relevant articles and documents

Method for Producing Asymmetric Conjugated Diyne Compound and Method for Producing Z,Z-Conjugated Diene Compound Using the Same

Provided are a method for efficiently producing an asymmetric conjugated diyne from an inexpensive and safe alternative compound to hydroxylamine hydrochloride and a method for producing a Z,Z-conjugated diene compound from the asymmetric conjugated diyne compound thus obtained. More specifically, provided is a method for producing an asymmetric conjugated diyne compound comprising a step of subjecting a terminal alkyne compound (1): HC≡C—Z1—Y1 to a coupling reaction with an alkynyl halide (2) Y2—Z2—C≡C—X by using sodium borohydride in water and an organic solvent in the presence of a copper catalyst and a base to obtain the asymmetric conjugated diyne compound (3): Y2—Z2—C≡C—C≡C—Z1—Y1. In addition, provided is a method for producing a Z,Z-conjugated diene compound by reducing the resulting asymmetric conjugated diyne compound, or the like.

Stereoselective Synthesis of a Potential Sex Pheromone of Stenoma Cecropia (Lepidoptera)

A convenient preparation of (Z,E) 9,11- and (Z,Z) 9,11-tetradecadien-1-yl and (9Z) 9,11-tetradecenyn-1-yl acetate, alcohol and aldehyde with 99.5percent stereoisomeric purity is described.The key step of this synthesis is the carbocupration of acetylene followed by palladium catalyzed cross coupling rection with the appropriate zinc reagent.

Pheromones. XXXIV. Synthesis of conjugated-unsaturated lepidoptera pheromones of analogues

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