54664-98-1

Basic information

• Product Name: (E,E)-tetradeca-9,11-dienyl acetate
• Synonyms: (E,E)-tetradeca-9,11-dienyl acetate;(9E,11E)-9,11-Tetradecadien-1-ol acetate;(Z,Z)-9,11-Tetradecadienyl acetate;(9E,11E)-9,11-Tetradecadien-1-yl acetate;9,11-Tetradecadien-1-ol, 1-acetate, (9E,11E)-;9,11-Tetradecadien-1-ol, acetate, (9E,11E)-;Einecs 259-287-8;(E,E)-9,11-Tetradecadien-1-ol acetate
• CAS NO: 54664-98-1
• Molecular Formula: C₁₆H₂₈O₂
• Molecular Weight: 252.39232
• EINECS: 259-287-8
• Mol File: 54664-98-1.mol
• Article Data: 9

Chemical Properties

• Boiling Point: 378.0±0.0℃ (760 Torr)
• Flash Point: 107.1±20.4℃
• Appearance: /
• Density: 0.890±0.06 g/cm3 (20 ºC 760 Torr)
• Vapor Pressure: 6.47E-06mmHg at 25°C
• Refractive Index: 1.4698 (23℃)
• CAS DataBase Reference: (E,E)-tetradeca-9,11-dienyl acetate(CAS DataBase Reference)
• NIST Chemistry Reference: (E,E)-tetradeca-9,11-dienyl acetate(54664-98-1)
• EPA Substance Registry System: (E,E)-tetradeca-9,11-dienyl acetate(54664-98-1)

Safety Data

• Hazardous Substances Data: 54664-98-1(Hazardous Substances Data)

Usage

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+

Upstream product

• 1576-87-0 trans-2-pentenal 
• 80625-80-5 Acetic acid 9-(triphenyl-λ⁵-phosphanylidene)-nonyl ester 
• 55136-52-2 pent-2-yn-1-al 
• 81744-94-7 7-tetrahydropyranyloxy-heptyl-magnesium chloride 
• 53596-83-1 1-tetrahydropyranyloxy-8-iodooctane 
• 86593-90-0 2-[8-((1R,2S,3R,5S,6R,7S)-5-Ethyl-4,4-dioxo-4λ⁶-thia-tricyclo[5.2.1.0^2,6]dec-8-en-3-yl)-octyloxy]-tetrahydro-pyran 
• 76934-44-6 C₂₃H₃₈O₄ 
• 70979-90-7 6-[(tetrahydro-2H-pyran-2-yl)oxy]-1-hexen-4-yn-3-ol, acetate 
• 76934-45-7 (2E,4Z)-Trideca-2,4-diene-1,13-diol 
• 81744-96-9 cis-tridec-4-en-2-yn-1,13 diol 
• 67886-17-3 7-(tetrahydropyran-2-xyloxy)heptylmagnesium bromide 
• 67818-16-0 (2E,4E)-2,4-Heptadienylacetat 
• 72553-57-2 (9E,11E)-9,11-Tetradecadienyl-(tetrahydro-2-pyranyl)ether 
• 106094-32-0 1-(2-tetrahydropyranyloxy)-10-(trimethylsilyl)-(Z)-9-decene 

Relevant articles and documents

PHOTOOXIDATION OF (Z,E)-9,11-TETRADECADIENYL ACETATE, THE MAIN COMPONENT OF THE SEX PHEROMONE OF THE FEMALE EGYPTIAN COTTON LEAFWORM (SPODOPTERA LITTORALIS)

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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.

A Stereospecific Synthesis of All Four Isomers of 9,11-Tetradecadienyl Acetate Using a General Method Applicable to 1,3-Dienes

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