28540-79-6 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.
Check Digit Verification of cas no
The CAS Registry Mumber 28540-79-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,5,4 and 0 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 28540-79:
(7*2)+(6*8)+(5*5)+(4*4)+(3*0)+(2*7)+(1*9)=126
126 % 10 = 6
So 28540-79-6 is a valid CAS Registry Number.
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+
28540-79-6Relevant articles and documents
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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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-chloroborepane, hydroborates 1-bromo-1-alkynes cleanly to provide the B-(cis-1-bromo-1-alkenyl)borepanes.Treatment of these intermediates with sodium methoxide results in the displacement of bromine by one end of the boracycloalkyl moiety, producing the corresponding vinylboranes, containing the eight-membered borocane moiety.These intermediates, on controlled protonolysis followed by oxidation, provide the (E)-7-alken-1-ols.This process constitutes a simple, very convenient, stereospecific and general one-pot synthesis of (E)-7-alken-1-ols.Pheromones, (E)-7-tetradecen-1-ol, (E)-7-tetradecen-1-ol acetate and (E)-7-dodecen-1-ol acetate were prepared in excellent yields.
Pheromones XXVIII. A stereoselective synthesis of (E)-olefinic sex pheromones of moths
Canevet,Roeder,Vostrowsky,Bestmann
, p. 1115 - 1120 (2007/10/02)
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