68900-86-7 Usage
Description
(E)-tetradec-3-enol, also known as (E)-3-tetradecen-1-ol, is a chemical compound with the molecular formula C14H28O. It is a colorless to pale yellow liquid characterized by a floral, waxy, and green odor. (E)-tetradec-3-enol is commonly found in natural products such as flowers, fruits, and vegetables, and is valued for its diverse applications across various industries.
Uses
Used in Flavor and Fragrance Industry:
(E)-tetradec-3-enol is used as a flavor and fragrance ingredient for its distinct floral, waxy, and green scent. It adds a pleasant aroma to various products in the food and cosmetic industries, enhancing their sensory appeal and consumer experience.
Used in Pest Control:
(E)-tetradec-3-enol is used as an insecticidal agent due to its potential insecticidal properties. It can be employed in the agricultural sector to control pests and protect crops, thereby increasing yield and reducing the need for chemical pesticides.
Used in Preservation:
(E)-tetradec-3-enol is used as a preservative in the food and cosmetic industries, thanks to its antimicrobial properties. It helps to extend the shelf life of products by inhibiting the growth of microorganisms, ensuring freshness and safety for consumers.
Used in Chemical Research:
(E)-tetradec-3-enol is used as a valuable compound in the chemical and scientific communities for research and development purposes. Its unique properties and versatility make it a promising candidate for the creation of new products and the advancement of scientific knowledge in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 68900-86-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,9,0 and 0 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 68900-86:
(7*6)+(6*8)+(5*9)+(4*0)+(3*0)+(2*8)+(1*6)=157
157 % 10 = 7
So 68900-86-7 is a valid CAS Registry Number.
InChI:InChI=1/C14H28O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15/h11-12,15H,2-10,13-14H2,1H3/b12-11+
68900-86-7Relevant articles and documents
Method for synthesizing cis-3-tetradecanoacetate and trans-3-tetradecanoacetate
-
, (2019/08/01)
The invention discloses a method for synthesizing cis-3-tetradecanoacetate and trans-3-tetradecanoacetate. The method comprises the following steps: (1) preparing 3-tetradecyne alcohol-1; (2) preparing cis-3-tetradecenol-1; (3) preparing trans-3-tetradecenol-1; and (4) preparing the cis-3-tetradecanoacetate and trans-3-tetradecanoacetate. The method is used for synthesizing cis-3-tetradecanoacetate and trans-3-tetradecanoacetate which are main components of gyplure of holcocerus insularis Staudinger; the raw materials for reaction are easily obtained; the cost is low; technical processes are short; reaction conditions are mild; the operation is simple, convenient and free from risk; the product is easily separated; the yield is high; and massive production can be carried out.
Short and stereoselective synthesis of (E)-3-alkenyl acetates, insect sex pheromone constituents of Lepidoptera; Gelechidae
Ragoussis, Valentine,Vamvaka, Ekaterini,Kolymbadi, Maria
, p. 398 - 399 (2007/10/03)
(E)-3-alkenyl acetates, which are insect sex pheromone constituents, have been prepared from linear saturated aldehydes, by a short three steps process, via the (E)-3-alkenoic acids and the corresponding (E)-3-alkenols, in good overall yield (60-65%) and high stereochemical purity (>99%).
SYNTHESIS OF 3E-TETRADECENOL, 3E,9E-TETRADECADIENOL, AND THEIR ACETATES STARTING FROM ACETYLCYCLOPROPANE
Ivanova, N. M.,Cheskis, B. A.,Rubanova, E. V.,Yatsynin, V. G.,Moiseenkov, A. M.,Nefedov, O. M.
, p. 557 - 561 (2007/10/02)
Stereospecific synthesis of the linear E-olefins mentioned in the title was realized by a general scheme that was worked out earlier by the authors and which includes as key step homologization of the corresponding aliphatic pentakisnoraldehydes by means of trimethylsilyloxyvinylcyclopropane and ZnBr2-initiated rearrangement of the intermediate cyclopropylcarbinols under the influence of Me3SiBr.
