51544-64-0 Usage
Description
(2E,4E,6Z)-methyl deca-2,4,6-trienoate, also known as (2E,4E,6Z)-2,4,6-Decatrienoic Acid Methyl Ester, is an organic compound with a specific molecular structure characterized by the presence of three carbon-carbon double bonds in the 2, 4, and 6 positions. It is a methyl ester derivative of deca-2,4,6-trienoic acid, which is an unsaturated fatty acid. (2E,4E,6Z)-methyl deca-2,4,6-trienoate has a distinct chemical profile and is known for its specific applications in the field of chemical ecology.
Uses
Used in Chemical Ecology:
(2E,4E,6Z)-methyl deca-2,4,6-trienoate is used as an attractant pheromone for the brown-winged green bug, Plautia stali. (2E,4E,6Z)-methyl deca-2,4,6-trienoate plays a crucial role in attracting the insects, which can be beneficial for monitoring and controlling their population in agricultural settings. By using this pheromone, researchers and farmers can effectively manage the presence of Plautia stali, which is known to be a pest in various crops.
Check Digit Verification of cas no
The CAS Registry Mumber 51544-64-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,5,4 and 4 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 51544-64:
(7*5)+(6*1)+(5*5)+(4*4)+(3*4)+(2*6)+(1*4)=110
110 % 10 = 0
So 51544-64-0 is a valid CAS Registry Number.
51544-64-0Relevant articles and documents
The geometric isomers of methyl-2,4,6-decatrienoate, including pheromones of at least two species of stink bugs
Khrimian, Ashot
, p. 3651 - 3657 (2007/10/03)
All eight geometric isomers of methyl 2,4,6-decatrienoate were synthesized from readily accessible starting materials by fully exploiting Wittig-type olefinations, and taking advantage of an easy separation of 2E and 2Z unsaturated esters. The aggregation pheromone of the brown-winged green bug, Plautia stali, methyl (E,E,Z)-2,4,6-decatrienoate (also a cross-attractant for the brown marmorated stink bug, Halyomorpha halys), was expediently produced in two easy steps from (E)-4,4-dimethoxy-2-butenal in 55% yield. The sex pheromone of the red-shouldered stink bug, Thyanta pallidovirens, methyl (E,Z,Z)-2,4,6-decatrienoate, was conveniently synthesized from 2,4-octadiyn-1-ol in 32% yield using in situ manganese dioxide oxidation-Wittig condensation in a key step.