35835-80-4 Usage
Uses
Used in Chemical Ecology:
cis-8-Tetradecen-1-olacetate is used as a chemical signal for [facilitating communication between the male and female greenheaded leafroller moths]. cis-8-Tetradecen-1-olacetate serves as a key component in the sex pheromone of the greenheaded leafroller moth, playing a crucial role in the mating process by attracting male moths to female moths.
Used in Pheromone-based Pest Control:
cis-8-Tetradecen-1-olacetate is used as an active ingredient in [developing pheromone-based traps and control strategies] for managing greenheaded leafroller moth populations. By mimicking the natural sex pheromone, cis-8-Tetradecen-1-olacetate can be employed to disrupt mating patterns, reducing the population of these pests and minimizing their impact on agriculture and forestry.
Used in Research and Development:
cis-8-Tetradecen-1-olacetate is used as a research tool for [studying the chemical ecology and behavior of various insect species]. Understanding the role of cis-8-Tetradecen-1-olacetate in insect communication can lead to the development of new strategies for pest control and provide insights into the complex world of insect pheromones.
Used in香水 (Perfumery) Industry:
cis-8-Tetradecen-1-olacetate is used as a fragrance ingredient for [creating unique and natural scent profiles] in the perfumery industry. Its distinct chemical structure contributes to a specific olfactory characteristic, which can be utilized to develop novel and appealing fragrances for various consumer products.
Check Digit Verification of cas no
The CAS Registry Mumber 35835-80-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,8,3 and 5 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 35835-80:
(7*3)+(6*5)+(5*8)+(4*3)+(3*5)+(2*8)+(1*0)=134
134 % 10 = 4
So 35835-80-4 is a valid CAS Registry Number.
InChI:InChI=1/C16H30O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-18-16(2)17/h7-8H,3-6,9-15H2,1-2H3/b8-7-
35835-80-4Relevant academic research and scientific papers
PHEROMONES OF INSECTS AND THEIR ANALOGS. XXI. SYNTHESIS OF ALK-8Z-EN-1-OLS AND THEIR ACETATES FROM A FUNCTIONALLY DIFFERENTIATED PRODUCT OF OZONOLYSIS OF CYCLOOCTENE
Odinokov, V. N.,Akhmetova, V. R.,Khasanov, Kh. D.,Abduvakhabov, A. A.,Tolstikov, G. A.,Panasenko, A. A.
, p. 240 - 243 (2007/10/02)
Dodec-8Z-en-1-ol (VIII) and tetradec-8Z-en-1-ol (IX) and the corresponding acetates (X and IX) - components of the sex pheromones of many species of Lepidoptera - have been synthesized from cyclooctene (I) in three stages.The ozonolysis of (I) ( -70 deg C, CH2Cl2-MeOH), NaHCO3; -20 deg C, Ac2O/Et3N) led to methyl 8-oxooctanoate (II).The DNPH of (II), (III), mp 59-61 deg C.The coupling of (II) with n-C3H17CH=PPh3 (IV) or with n-C5H11CH=PPh3 (V) (-70 deg C , 2h; 25 deg C, 15h, Ar) gave the methyl esters of dodec-8Z-enoic (VI) and tetradec-8Z-enoic (VII) acids, respectively.The reduction of (VI) and (VII) gave the corresponding alcohols (VIII) and (IX) by the acetylation (Ac2O-Py, 25 deg C, 24h) of which, (X) and (XI) , were obtained.The yields (percent): (II) 80, (VI) 45, (VII) 60, (VIII) 95, (IX) 90, (X) 75, (XI) 74.The IR and PMR spectra of compounds (II) and (VI-XI) are given.
