(E)-tetradec-7-enyl acetate

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Quality manufacturer supply (E)-tetradec-7-enyl acetate 28540-79-6 in stock with high standard

  • Molecular Formula: C16H30 O2
  • Molecular Weight: 254.413
  • Vapor Pressure: 0.000136mmHg at 25°C 
  • Boiling Point: 333.5°Cat760mmHg 
  • Flash Point: 98.5°C 
  • PSA: 26.30000 
  • Density: 0.878g/cm3 
  • LogP: 5.02660 

(E)-tetradec-7-enyl acetate(Cas 28540-79-6) Usage

General 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. Its chemical structure consists of a long hydrocarbon chain with a double bond and an acetate group. This chemical is commonly found in a variety of natural sources, including pheromones of insects, fruits, and plants. It is known for its sweet, fruity odor and is often used in the production of perfumes, soaps, and other fragrances. Additionally, (E)-tetradec-7-enyl acetate has been studied for its potential insecticidal properties, as it has been shown to have activity against certain insect pests. Overall, this compound has a range of applications in the fragrance and agricultural industries.

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+

28540-79-6 Relevant articles

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

Hayashi,Midorikawa

, p. 100 - 102 (1975)

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Pheromones via Organoboranes. 3. Vinylic Organoboranes. 10. Stereospecific Synthesis of (Z)- and (E)-6- and -7-Alken-1-ols via Boracyclanes

Brown, Herbert C.,Basavaiah, Deevi,Singh, Shankar M.,Bhat, Narayan G.

, p. 246 - 250 (2007/10/02)

Treatment of B-(E)-1-alkenylborinanes, o...

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

Zakharkin, L. I.,Petrushkina, E. A.

, p. 1419 - 1422 (2007/10/02)

The stereospecific synthesis of 7E- and ...

PHEROMONE SYNTHESIS VIA ORGANOBORANES: A STEREOSPECIFIC SYNTHESIS OF (E)-7-ALKEN-1-OLS

Basavaiah, Deevi

, p. 153 - 156 (2007/10/02)

Borepane, obtained via hydridation of B-...

INSECT SEX PHEROMONES. STEREOSELECTIVE SYNTHESIS OF SEVERAL (Z)- AND (E)-ALKEN-1-OLS, THEIR ACETATES, AND OF (9Z,12E)-9,12-TETRADECADIEN-1-YL ACETATE

Rossi, Renzo,Carpita, Adriano,Gaudenzi, Loretta,Quirici, Maria Grazia

, p. 237 - 246 (2007/10/02)

Several female sex pheromone components ...

28540-79-6 Process route

(7E)-tetradec-7-en-1-ol
37011-95-3

(7E)-tetradec-7-en-1-ol

acetyl chloride
75-36-5

acetyl chloride

E-7-tetradecen-1-yl acetate
28540-79-6

E-7-tetradecen-1-yl acetate

Conditions
Conditions Yield
With pyridine; In benzene;
93%
(7E)-tetradec-7-en-1-ol
37011-95-3

(7E)-tetradec-7-en-1-ol

acetic anhydride
108-24-7

acetic anhydride

E-7-tetradecen-1-yl acetate
28540-79-6

E-7-tetradecen-1-yl acetate

Conditions
Conditions Yield
With pyridine; In diethyl ether;
95%
In pyridine; for 1h; Heating;
90%
With pyridine;

28540-79-6 Upstream products

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  • 75-36-5
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    acetyl chloride

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    Tetradec-7-en-1-ol-acetat

  • 37011-95-3
    37011-95-3

    (7E)-tetradec-7-en-1-ol

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