28540-79-6

Basic information

• Product Name: (E)-tetradec-7-enyl acetate
• Synonyms: (E)-tetradec-7-enyl acetate;Acetic acid [(E)-7-tetradecen-1-yl] ester
• CAS NO: 28540-79-6
• Molecular Formula: C₁₆H₃₀O₂
• Molecular Weight: 254.4082
• EINECS: 249-072-7
• Mol File: 28540-79-6.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 333.5°Cat760mmHg
• Flash Point: 98.5°C
• Appearance: /
• Density: 0.878g/cm³
• Vapor Pressure: 0.000136mmHg at 25°C
• Refractive Index: 1.45
• CAS DataBase Reference: (E)-tetradec-7-enyl acetate(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-tetradec-7-enyl acetate(28540-79-6)
• EPA Substance Registry System: (E)-tetradec-7-enyl acetate(28540-79-6)

Safety Data

• Hazardous Substances Data: 28540-79-6(Hazardous Substances Data)

Usage

Description

(E)-tetradec-7-enyl acetate is a chemical compound that belongs to the class of organic compounds known as long-chain fatty acid esters. It is characterized by a long hydrocarbon chain with a double bond and an acetate group. (E)-tetradec-7-enyl acetate is commonly found in natural sources such as insect pheromones, fruits, and plants, and is recognized for its sweet, fruity odor.

Uses

Used in Fragrance Industry:
(E)-tetradec-7-enyl acetate is used as a fragrance ingredient for its sweet, fruity scent. It is commonly utilized in the production of perfumes, soaps, and other fragrances to provide a pleasant and attractive aroma.
Used in Agricultural Industry:
(E)-tetradec-7-enyl acetate is used as a potential insecticide for its activity against certain insect pests. It has been studied for its insecticidal properties, which could be beneficial in controlling and managing insect populations that may be harmful to crops or the environment.

InChI:InChI=1/C16H30O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-18-16(2)17/h8-9H,3-7,10-15H2,1-2H3/b9-8+

Upstream product

• 55305-38-9 (E)-2-(tetradec-7-en-1-yloxy)tetrahydro-2H-pyran 
• 75-36-5 acetyl chloride 
• 16974-33-7 Tetradec-7-en-1-ol-acetat 
• 37011-95-3 (7E)-tetradec-7-en-1-ol 
• 108-24-7 acetic anhydride 
• 52957-07-0 (7E)-tetradec-7-enioc acid 
• 37011-92-0 (E)-6-Tridecen-1-ol 
• 83748-49-6 1-bromo-6E-tridecene 
• 15972-89-1 (E)-1-phenoxy-2,7-octadiene 
• 693-25-4 n-pentylmagnesium bromide 
• 83748-47-4 (E)-1,6-tridecadiene 
• 2009-84-9 (chloro-6' hexyloxy)-2 tetrahydropyranne 
• 37043-40-6 2-(tetradec-7-yn-1-yloxy)tetrahydro-2H-pyran 
• 2009-83-8 6-chloro-1-hexanol 

Relevant articles and documents

A novel stereoselective synthesis of alkenol sex pheromones via [3,3] sigmatropic rearrangement of allylic dithiocarbamates

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STEREOSPECIFIC SYNTHESIS OF PHEROMONES OF THE E-ALKENE SERIES FROM THE TELOMER OF BUTADIENE WITH PHENOL

The stereospecific synthesis of 7E- and 9E-dodecenyl acetates, 7E- and 11E-tetradecenyl acetates, 11E-tetradecen-1-ol, and 11E-hexadecenyl acetate, i.e., E-olefinic sex pheromones, was realized from 1-phenoxy-2E,7-octadiene (the telomer of butadiene with phenol).

Pheromones XXVIII. A stereoselective synthesis of (E)-olefinic sex pheromones of moths

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