19926-63-7 Usage
Uses
Used in Fragrance Industry:
(Z,Z,E)-3,6,8-Dodecatrien-1-ol is used as a fragrance ingredient for its scent that mimics natural sebaceous secretions, adding a unique and appealing aroma to various products.
Used in Food and Beverage Industry:
(Z,Z,E)-3,6,8-Dodecatrien-1-ol is used as a flavoring agent to enhance the taste and aroma of food and beverages, providing a distinct flavor profile.
Used in Personal Care Industry:
(Z,Z,E)-3,6,8-Dodecatrien-1-ol is used as an ingredient in personal care products, such as perfumes, lotions, and creams, to impart a pleasant scent and improve the overall sensory experience.
Used in Cleaning Products Industry:
(Z,Z,E)-3,6,8-Dodecatrien-1-ol is used in cleaning products to provide a fresh and natural scent, enhancing the user's experience and making the cleaning process more enjoyable.
Check Digit Verification of cas no
The CAS Registry Mumber 19926-63-7 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 3 respectively.
Calculate Digit Verification of CAS Registry Number 19926-63:
(7*1)+(6*9)+(5*9)+(4*2)+(3*6)+(2*6)+(1*3)=147
147 % 10 = 7
So 19926-63-7 is a valid CAS Registry Number.
19926-63-7Relevant academic research and scientific papers
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.
