89353-62-8 Usage
Description
(3Z,6Z,9Z)-3,6,9-Nonadecatriene, a long-chain hydrocarbon and a member of the polyunsaturated fatty acid family, is a chemical compound with 19 carbon atoms and three double bonds in the Z configuration at the 3rd, 6th, and 9th carbon positions. It is commonly found in plant oils, such as citrus fruits, and contributes to their characteristic aroma.
Uses
Used in the Food Industry:
(3Z,6Z,9Z)-3,6,9-Nonadecatriene is used as a natural flavor enhancer for its characteristic aroma derived from plant oils, particularly citrus fruits.
Used in the Fragrance Industry:
(3Z,6Z,9Z)-3,6,9-Nonadecatriene is used as a natural fragrance enhancer for its distinct aroma, adding a pleasant scent to various products.
Used in the Health and Wellness Industry:
(3Z,6Z,9Z)-3,6,9-Nonadecatriene is studied for its potential health benefits, including its anti-inflammatory and anti-cancer properties, making it a promising candidate for pharmaceutical applications.
Check Digit Verification of cas no
The CAS Registry Mumber 89353-62-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,3,5 and 3 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 89353-62:
(7*8)+(6*9)+(5*3)+(4*5)+(3*3)+(2*6)+(1*2)=168
168 % 10 = 8
So 89353-62-8 is a valid CAS Registry Number.
InChI:InChI=1/C19H34/c1-3-5-7-9-11-13-15-17-19-18-16-14-12-10-8-6-4-2/h5,7,11,13,17,19H,3-4,6,8-10,12,14-16,18H2,1-2H3/b7-5-,13-11-,19-17-
89353-62-8Relevant articles and documents
A nine carbon homologating system for skip-conjugated polyenes
Mustafa, Hussein H.,Baird, Mark S.,Al Dulayymi, Juma'A R.,Tverezovskiy, Viacheslav V.
, p. 34 - 42 (2014/07/08)
Ozonolysis of Z,Z,Z-cylonona-1,4,7-triene leads to a 1,9-difunctionalised Z,Z-3,6-nonadiene which is readily converted into a range of polyunsaturated pheromones and fatty acids.
Use of the anti-oxidant butylated hydroxytoluene in situ for the synthesis of readily oxidized compounds: Application to the synthesis of the moth pheromone (Z,Z,Z)-3,6,9-nonadecatriene
Davies, Noel W.,Meredith, Graham,Molesworth, Peter P.,Smith, Jason A.
, p. 848 - 849 (2008/03/12)
The triene (Z,Z,Z)-3,6,9-nonadecatriene was synthesized in three steps from methyl linolenate. The key to the synthesis was the use of the anti-oxidant butylated hydroxytoluene in situ to provide protection of the unstable triene from autoxidation during reaction workup. This simple modification resulted in an increase in the yield from 20 to 85% over three steps. CSIRO 2007.
Identification and enantioselective synthesis of (Z,Z)-6,9-c/s-3S,4R-epoxynonadecadiene, the major sex pheromone component of Boarmia selenaria
Becker
, p. 4923 - 4926 (2007/10/02)
(Z,Z)-6,9-cis-3S,4R-Epoxynonadecadiene has been identified as the major sex pheromone component of the Geometrid Boarmia selenaria. A short and efficient synthesis of the chiral methylene-interrupted diene-epoxide has been developed for both enantiomers.
