35746-21-5 Usage
Description
E-11-TETRADECENAL, also known as (E)-Tetradec-11-enal, is an organic compound that serves as a sex pheromone component. It is primarily found in the female spruce budworm, Choristoneura Fumiferana, and plays a crucial role in attracting male counterparts for mating purposes. E-11-TETRADECENAL has a distinct aldehyde functional group and a long hydrocarbon chain, which contribute to its unique chemical properties and biological function.
Uses
Used in Pheromone-based Pest Management:
E-11-TETRADECENAL is used as a pheromone component in pest management strategies, specifically targeting the spruce budworm. By mimicking the natural sex pheromone released by female spruce budworms, this compound can be employed to attract and monitor the presence of male spruce budworms in affected areas. This approach helps in controlling pest populations and reducing the damage caused by these insects to forests and agricultural crops.
Used in Chemical Ecology Research:
E-11-TETRADECENAL is also utilized in chemical ecology research to study the behavior and communication mechanisms of various insect species. Understanding the role of pheromones in insect mating and aggregation can provide valuable insights into the development of novel pest control methods and the conservation of ecosystems.
Used in Fragrance and Flavor Industry:
Due to its unique chemical structure and properties, E-11-TETRADECENAL can be used as a raw material in the fragrance and flavor industry. It can contribute to the development of new scents and flavors, enhancing the sensory experience of various products.
Hazard
Low toxicity by ingestion, inhalation, and
skin contact.
Check Digit Verification of cas no
The CAS Registry Mumber 35746-21-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,7,4 and 6 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 35746-21:
(7*3)+(6*5)+(5*7)+(4*4)+(3*6)+(2*2)+(1*1)=125
125 % 10 = 5
So 35746-21-5 is a valid CAS Registry Number.
InChI:InChI=1S/C14H26O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15/h3-4,14H,2,5-13H2,1H3/b4-3+
35746-21-5Relevant articles and documents
Production of pheromones and fragrances from substituted and unsubstituted 1-alken-3yl alkylates
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Page/Page column 6-7, (2010/05/13)
Compounds of the formula (I) wherein R2 is a branched or unbranched, saturated or ethylenically mono or di unsaturated aliphatic radical, Z is —CH2OH, —CH2OAc or —CHO, m is a whole positive integer of one or more, and Ac is an acetyl group are synthesized by a process wherein a 1-alken-3-yl alkylate, is reacted with a halo alkanol Grignard reagent.
Stereospecific synthesis of 11E-tetradecenal, 11E-tetradecen-1-ol, and its acetate, pheromone components of insects of Lepidoptera order, from 10-undecenoic acid
Ishmuratov,Yakovleva,Kharisov,Muslukhov,Tolstikov
, p. 1035 - 1037 (2007/10/03)
A regio-and stereospecific synthesis of 11E-tetradecen-1-ol and its derivatives, which are pheromone components of many insect species of Lepidoptera order, by means of a reaction of methylmagnesium cuprate reagent with 1,12-tridecadien-3-yl acetate by the SN2' mechanism, was carried out.
Kolbe electrosynthesis of (E)-11-tetradecenal-The sex pheromone of eastern spruce budworm (Choristoneura of fumiferana)
Singh, Krishna Nand,Singh, Manorama,Misra, Ram Achal
, p. 867 - 868 (2007/10/02)
The synthesis of (E)-11-tetradecenal (7), a potent lepidoptera sex pheromone is reported employing the modified Knoevenagel condensation and Kolbe electrolysis in the key steps.
