40642-42-0 Usage
Description
(9Z)-9-Tetradecene-14-ol is a naturally occurring organic compound that belongs to the class of secondary alcohols. It is characterized by the presence of a double bond at the 9th carbon atom (Z-configuration) and a hydroxyl group at the 14th carbon atom in its tetradecene (14-carbon) chain. (9Z)-9-Tetradecene-14-ol is known for its unique chemical properties and potential applications in various industries.
Uses
Used in the Food Industry:
(9Z)-9-Tetradecene-14-ol is used as an intermediate in the synthesis of 2-substituted cyclobutanones, which serve as markers for the detection of γ-irradiation in lipid-containing foods. (9Z)-9-Tetradecene-14-ol plays a crucial role in ensuring food safety and quality by indicating the exposure of these foods to ionizing radiation, which is a common method used for sterilization and preservation.
Used in the Chemical Synthesis Industry:
(9Z)-9-Tetradecene-14-ol can be utilized as a building block or starting material for the synthesis of various chemical compounds, including pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structure and functional groups make it a valuable component in the development of new molecules with specific properties and applications.
Used in the Cosmetics Industry:
Due to its alcohol nature, (9Z)-9-Tetradecene-14-ol may find applications in the formulation of cosmetics and personal care products. It could be used as an emollient, moisturizer, or viscosity modifier, contributing to the texture, feel, and performance of these products.
Used in the Research and Development Sector:
(9Z)-9-Tetradecene-14-ol can be employed as a research tool in various scientific studies, particularly in the fields of organic chemistry, biochemistry, and materials science. It may be used to investigate the properties of secondary alcohols, study the effects of double bonds on molecular behavior, or explore the potential of this compound in the development of new materials and technologies.
Check Digit Verification of cas no
The CAS Registry Mumber 40642-42-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,6,4 and 2 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 40642-42:
(7*4)+(6*0)+(5*6)+(4*4)+(3*2)+(2*4)+(1*2)=90
90 % 10 = 0
So 40642-42-0 is a valid CAS Registry Number.
40642-42-0Relevant articles and documents
Synthesis of deuterated 5(Z),11(Z)-eicosadienoic acid as a biomarker for trophic transfer
Albu, Siliva,Sverko, Ed,Arts, Michael T.,Capretta, Alfredo
scheme or table, p. 787 - 788 (2011/03/21)
The poly-methylene interrupted fatty acid 5(Z),11(Z)-eicosadienoic acid and its tetradeuterated analogue were prepared via a convergent synthetic sequence.
Synthesis of (Z)-5-dodecenyl and (Z)-5-tetradecenyl acetates: Pheromone components of Lepidoptera noctuidae species
Kelkar, S. V.,Reddy, G. Bhaskar,Kulkarni, G. H.
, p. 980 - 981 (2007/10/02)
(Z)-5-Dodecenyl acetate (1) and (Z)-5-tetradecenyl acetate (2), the pheromone components of Lepidoptera noctuidae species have been synthesised by a new approach from the corresponding (Z)-4-undecenol (3) and (Z)-4-tridecenol (4), both of which have been obtained from a common intermediate, viz. the dianion of 4-pentyn-1-ol.
PHEROMONE XXX. IDENTIFIZIERUNG EINES NEUARTIGEN PHEROMONKOMPLEXES AUS DER GRASEULE SCOTIA EXCLAMATIONIS (LEPIDOPTERA).
Bestmann, H. J.,Brosche, T.,Koschatzky, K. H.,Michaelis, K.,Platz, H.,et. al.
, p. 747 - 750 (2007/10/02)
Mittels Gaschromatographie und GC-Massenspektrometrie wurden (7)-5-Tetradecenylacetat und (Z)-9-Tetradecenylacetat als Pheromonkomplex bei der Graseule identifiziert.
