82970-94-3 Usage
Description
(3Z,6Z,9Z)-nonadeca-1,3,6,9-tetraene, a chemical compound with a long hydrocarbon chain containing 19 carbon atoms and four double bonds in a specific arrangement, belongs to the family of polyunsaturated fatty acids. It is commonly found in various plant oils and animal fats and plays a crucial role in human health as a precursor for the synthesis of essential fatty acids. Involved in numerous physiological processes, it also exhibits potential pharmacological activities, including anti-inflammatory and anti-cancer properties.
Uses
Used in Pharmaceutical Industry:
(3Z,6Z,9Z)-nonadeca-1,3,6,9-tetraene is used as a precursor for the synthesis of essential fatty acids, which are vital for human health. Its involvement in various physiological processes and potential pharmacological activities, such as anti-inflammatory and anti-cancer properties, make it a valuable compound for the development of pharmaceutical products.
Used in Dietary Supplements Industry:
(3Z,6Z,9Z)-nonadeca-1,3,6,9-tetraene is used as an ingredient in dietary supplements due to its role as a precursor for essential fatty acids. Its presence in plant oils and animal fats makes it a natural and beneficial addition to supplements aimed at promoting overall health and well-being.
Used in Research and Development:
(3Z,6Z,9Z)-nonadeca-1,3,6,9-tetraene is used as a subject of study in research and development for its potential applications in various fields, including medicine, nutrition, and pharmaceuticals. Its unique chemical structure and properties provide insight into its function and potential uses, driving further innovation and development in these industries.
Check Digit Verification of cas no
The CAS Registry Mumber 82970-94-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,9,7 and 0 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 82970-94:
(7*8)+(6*2)+(5*9)+(4*7)+(3*0)+(2*9)+(1*4)=163
163 % 10 = 3
So 82970-94-3 is a valid CAS Registry Number.
82970-94-3Relevant articles and documents
Improved Synthesis of (3E,6Z,9Z)-1,3,6,9-Nonadecatetraene, Attraction Inhibitor of Bruce Spanworm, Operophtera bruceata, to Pheromone Traps for Monitoring Winter Moth, Operophtera brumata
Khrimian, Ashot,Lance, David R.,Mastro, Victor C.,Elkinton, Joseph S.
experimental part, p. 1828 - 1833 (2010/08/19)
The winter moth, Operophtera brumata (Lepidoptera: Geometridae), is an early-season defoliator that attacks a wide variety of hardwoods and, in some cases, conifers. The insect is native to Europe but has become established in at least three areas of Nort
SYNTHETIC STUDIES IN THE FIELD OF ATTRACTIVE SUBSTANCES (SEX ATTRACTANTS) OF INSECTS. SYNTHESIS OF NONADECA-1,cis-3,cis-6,cis-9-TETRAENE - THE SEX PHEROMONE OF Operophtera brumata (LEPIDOPTERA; GEOMETRIDAE)
Nikolaeva, L. A.,Kovalev, B. G.,Ishchenko, R. I.
, p. 103 - 105 (2007/10/02)
A new synthesis of nonadeca-1,cis-3,cis-6,cis-9-tetraene, the sex pheromone of the winter moth Operophtera brumata, has been developed which involves the alkylation of bromomagnesium derivatives of tetrahydropyranyl ethers of mono- and diacetylenic alcohols by a monoacetylenic bromide, followed by hydrogenation of the resulting triynol to a trienol, oxidation of the latter to an aldehyde, and interaction of the latter with methylenetriphenylphosphorane.
Pheromones, 57.- Synthesis of Lepidoptera Polyene Pheromones and of Structural Analogs.- Acetylenic Synthesis, Wittig Olefination, and Kolbe Electrolysis
Bestmann, Hans Juergen,Roth, Kurt,Michaelis, Karl,Vostrowsky, Otto,Schaefer, Hans J.,Michaelis, Ralf
, p. 417 - 422 (2007/10/02)
By a combination of acetylenic syntheses with Wittig olefination as well as by mixed Kolbe electrolysis alkadienes, alkatrienes, and alkatetraenes (sex attractants of Lepidoptera and structural analogs)were synthesized.
