63025-02-5 Usage
Uses
Used in Perfumery and Flavor Industry:
(Z,E)-tetradeca-9,11-dien-1-ol is utilized as a key ingredient in the creation of perfumes and flavors due to its unique and characteristic odor. Its natural presence in certain plants and animals contributes to the authenticity and complexity of the scents and tastes in these products.
Used in Pharmaceutical Industry:
As a phytosterol, (Z,E)-tetradeca-9,11-dien-1-ol is used in the pharmaceutical industry for its role in cell membrane function and as a precursor to steroid hormones. Its presence in formulations can contribute to the regulation of various physiological processes.
Used in Agriculture and Pest Control:
(Z,E)-tetradeca-9,11-dien-1-ol is employed as an antimicrobial and insecticidal agent in agricultural applications. Its natural properties help control pests and diseases, promoting healthier crop growth and reducing the need for chemical pesticides.
Used in Cosmetics Industry:
In the cosmetics industry, (Z,E)-tetradeca-9,11-dien-1-ol is used for its beneficial effects on skin health. As a component of cell membranes and a precursor to hormones, it can contribute to the development of skincare products that promote skin hydration, elasticity, and overall health.
Used in Research and Development:
(Z,E)-tetradeca-9,11-dien-1-ol is also used in research settings to study its potential biological activities further. Scientists explore its antimicrobial, insecticidal, and other properties to discover new applications and improve existing ones across various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 63025-02-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,0,2 and 5 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 63025-02:
(7*6)+(6*3)+(5*0)+(4*2)+(3*5)+(2*0)+(1*2)=85
85 % 10 = 5
So 63025-02-5 is a valid CAS Registry Number.
InChI:InChI=1/C14H26O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15/h3-6,15H,2,7-14H2,1H3/b4-3-,6-5+
63025-02-5Relevant academic research and scientific papers
THE WITTIG REACTION: COMMENTS ON THE MECHANISM AND APPLICATION AS A TOOL IN THE SYNTHESIS OF CONJUGATED DIENES
Ideses, Rut,Shani, Arnon
, p. 3523 - 3534 (2007/10/02)
For construction, by the Wittig reaction, of conjugated dienes with specific stereochemistry (either Z or E) at the newly formed double bond, without isomerization of the existing ("old") double bond, it is better to react a reactive (nonstabilized) saturated ylide with an α,β-unsaturated aldehyde.The opposite approach, namely, the reaction of a moderate (semi-stabilized) allylic ylide with a saturated aldehyde produces a mixture of geometric isomers, as a result of increased production of the E-configuration at the new double bond, and significant isomerization of the existing double bond.The proposed betaine structure for the intermediate could account only for the two equivalents of Li reaction.In other reactions, the less stable erythro-oxaphosphetane is probably the intermediate, produced by an early anti- or gauche C-C bond formation from the ylide and the carbonyl, from which the Z-double bond is then formed.
