34010-15-6 Usage
Description
CIS-11-TETRADECEN-1-OL, also known as (11Z)-Tetradecen-1-ol, is a long-chain fatty alcohol that can be synthesized in yeast through the heterogenous expression of genes involved in insect pheromone production. CIS-11-TETRADECEN-1-OL plays a significant role in the biosynthesis of pheromones in insects, where it is believed to be involved in the formation of acetates from acetyl-CoA and fatty alcohols.
Uses
Used in Insect Pheromone Production:
CIS-11-TETRADECEN-1-OL is used as a key component in the production of insect pheromones. It is involved in the biosynthesis process, where acetyltransferases catalyze the formation of acetates from acetyl-CoA and fatty alcohols, such as CIS-11-TETRADECEN-1-OL, to create pheromones that are essential for insect communication and mating.
Used in Chemical Synthesis:
CIS-11-TETRADECEN-1-OL can be used as a starting material or intermediate in the synthesis of various chemical compounds, including fragrances, flavors, and other specialty chemicals. Its unique structure and properties make it a valuable building block for creating a wide range of products.
Used in Research and Development:
As a compound involved in insect pheromone production, CIS-11-TETRADECEN-1-OL is also used in research and development to study the biological processes and mechanisms underlying insect communication, mating behavior, and chemical ecology. This knowledge can be applied to develop novel pest control strategies, improve agricultural practices, and enhance our understanding of insect biology.
Used in Pharmaceutical Industry:
CIS-11-TETRADECEN-1-OL may have potential applications in the pharmaceutical industry, particularly in the development of new drugs targeting insect-related diseases or conditions. Its role in pheromone biosynthesis could provide insights into the development of novel compounds with insecticidal or repellent properties, which could be used to combat insect-borne diseases or control pest populations.
Synthesis Reference(s)
Tetrahedron Letters, 36, p. 1141, 1995 DOI: 10.1016/0040-4039(94)02441-D
Check Digit Verification of cas no
The CAS Registry Mumber 34010-15-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,0,1 and 0 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 34010-15:
(7*3)+(6*4)+(5*0)+(4*1)+(3*0)+(2*1)+(1*5)=56
56 % 10 = 6
So 34010-15-6 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/h3-4,15H,2,5-14H2,1H3/b4-3-
34010-15-6Relevant articles and documents
SYNTHESIS OF STRAIGHT-CHAIN LEPIDOPTERAN PHEROMONES THROUGH ONE- OR TWO- CARBON HOMOLOGATION OF FATTY ALKENES
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, (2020/02/14)
Methods for the preparation of alkenes including insect pheromones are described. The methods include homologation reactions employing reagents such as 1,3-diesters, epoxides, cyanoacetates, and cyanide salts for elongation of starting materials and intermediates by one or two carbon atoms. The alkenes include insect pheromones useful in a number of agricultural applications.
SYNTHESIS OF Z-OLEFIN-CONTAINING LEPIDOPTERAN INSECT PHEROMONES
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Paragraph 0189; 0190, (2013/09/12)
The present invention is directed to methods of synthesizing insect pheromones, particularly lepidopteran insect pheromones, their precursors and derivatives from inexpensive, readily available starting materials using olefin metathesis catalysis.
Remarkable regioselective hydroboration of terminal alkenes by calcium borohydride
Narasimhan,Prasad, K. Ganeshwar,Madhavan
, p. 1141 - 1144 (2007/10/02)
Calcium borohydride is found to hydroborate unsaturated systems in the presence of ethyl acetate. The reaction exhibits remarkable selectivity towards terminal double bonds. Several Z-11-alken-1-ol pheromones are synthesized using this method.
