19926-64-8 Usage
Description
(Z,E,E)-3,6,8-Dodecatrien-1-ol, a member of the long-chain aliphatic compounds, is a chemical compound derived from plants. It is characterized by its pleasant, fruity odor and is commonly found in fruits and vegetables. This organic compound is known for its aromatic properties, making it a valuable ingredient in the flavoring, fragrance, and cosmetics industries.
Uses
Used in Flavoring Industry:
(Z,E,E)-3,6,8-Dodecatrien-1-ol is used as a flavoring agent for its pleasant, fruity odor, adding a natural taste to various food products.
Used in Fragrance Industry:
(Z,E,E)-3,6,8-Dodecatrien-1-ol is used as a fragrance ingredient in the production of perfumes and colognes, contributing to their appealing scents.
Used in Cosmetics and Personal Care Industry:
(Z,E,E)-3,6,8-Dodecatrien-1-ol is used as a chemical intermediate in the synthesis of other compounds, which are then utilized in the manufacturing of various cosmetics and personal care products.
Used in Chemical Synthesis:
(Z,E,E)-3,6,8-Dodecatrien-1-ol is used as a chemical intermediate for the synthesis of other compounds, showcasing its versatility in different applications across various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 19926-64-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,9,2 and 6 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 19926-64:
(7*1)+(6*9)+(5*9)+(4*2)+(3*6)+(2*6)+(1*4)=148
148 % 10 = 8
So 19926-64-8 is a valid CAS Registry Number.
InChI:InChI=1/C12H20O/c1-2-3-4-5-6-7-8-9-10-11-12-13/h4-7,9-10,13H,2-3,8,11-12H2,1H3/b5-4+,7-6-,10-9-
19926-64-8Relevant articles and documents
Selective Proton Transfer of Unsaturated Esters. Syntheses of A Trail-Following Pheromone for Subterranean Termites and Megatomoic Acid
Ikeda, Yoshihiko,Ukai, Junzo,Ikeda, Nobuo,Yamamoto, Hisashi
, p. 743 - 754 (1987)
Deconjugative protonation of dienolates from (E)-2-alkenoate using potassium disilazide as the base gives (Z)-3-alkenoate predominantly.A trail-following pheromone for subterranean termites is synthesized stereoselectively with this method.Deconjugative protonation of trienolates from (E,E)-2,4-tetradecadienoates gives (E,Z)-3,5-tetradecanoates which is hydrolyzed to give Megatomoic acid, a sex pheromone for a black carpet beetle Attagenus megatoma.
Syntheses and NMR analyses of the eight geometric isomers of 3,6,8-dodecatrien-1-ol, subterranean termite trail pheromone
Eya, Bryan K.,Otsuka, Toshikazu,Kubo, Isao,Wood, David L.
, p. 2695 - 2706 (2007/10/02)
Eight geometric isomers of 3,6,8-dodecatrien-1-ol 1, the trail-following pheromone of subterranean termites (Reticulitermes sp. Banks), were synthesized via a Wittig olefination reaction. The convergent syntheses of 1 consisted of a combination of two fragments, each containing an olefin with a fixed configuration, by formation of a third double bond to give a mixture of two geometric isomers. The mixtures of 1 were resolved by recycle high-performance liquid chromatography methods. 1H and 13C NMR peak assignments of the individual isomers were accomplished by homonuclear COSY, and one-bond CH correlation spectroscopy.
