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42521-46-0

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42521-46-0 Usage

Description

(9Z,12E)-9,12-Tetradecadien-1-ol, also known as (9Z,12E)-Tetradecadien-1-ol, is a naturally occurring organic compound that belongs to the class of alkenes. It is characterized by the presence of two carbon-carbon double bonds at the 9th and 12th positions, with the Z and E geometric isomers indicating the configuration of the double bonds. (9Z,12E)-9,12-Tetradecadien-1-ol is known for its unique chemical properties and potential applications in various fields.

Uses

Used in Biological Studies:
(9Z,12E)-9,12-Tetradecadien-1-ol is used as a key compound in the biological study of sequence, identification, and functional characterization of sex pheromone receptors in beet armyworms. Its role in these studies is crucial for understanding the chemical communication and mating behavior of these insects, which can have significant implications for pest management and agricultural practices.
Used in Chemical Research:
(9Z,12E)-9,12-Tetradecadien-1-ol can also be utilized in chemical research as a starting material or intermediate for the synthesis of various complex organic molecules. Its unique structure and functional groups make it a valuable building block for the development of new compounds with potential applications in pharmaceuticals, agrochemicals, and other industries.
Used in Pheromone Production:
In the field of chemical ecology, (9Z,12E)-9,12-Tetradecadien-1-ol can be employed in the production of pheromones, which are chemical signals used by animals for communication. (9Z,12E)-9,12-Tetradecadien-1-ol's ability to mimic or interact with sex pheromone receptors in specific insect species can be harnessed for the development of pheromone-based pest control strategies, reducing the reliance on chemical pesticides and promoting more sustainable agricultural practices.
Used in Fragrance Industry:
Due to its unique chemical structure and properties, (9Z,12E)-9,12-Tetradecadien-1-ol can be used as a component in the fragrance industry. It can contribute to the development of new and innovative scents, adding complexity and depth to perfumes, colognes, and other fragrance products.

Check Digit Verification of cas no

The CAS Registry Mumber 42521-46-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,5,2 and 1 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 42521-46:
(7*4)+(6*2)+(5*5)+(4*2)+(3*1)+(2*4)+(1*6)=90
90 % 10 = 0
So 42521-46-0 is a valid CAS Registry Number.

42521-46-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name Tetradeca-cis-9,trans-12-dien-1-ol

1.2 Other means of identification

Product number -
Other names (9Z,12E)-tetradeca-9,12-dien-1-ol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:42521-46-0 SDS

42521-46-0Relevant articles and documents

SYNTHESIS OF PHEROMONES AND RELATED MATERIALS VIA OLEFIN METATHESIS

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Paragraph 0110, (2018/09/12)

Methods for preparation of olefins, including 8- and 11-unsaturated monoenes and polyenes, via transition metathesis-based synthetic routes are described. Metathesis reactions in the methods are catalyzed by transition metal catalysts including tungsten-, molybdenum-, and ruthenium-based catalysts. The olefins include insect pheromones useful in a number of agricultural applications.

SYNTHESIS OF Z-OLEFIN-CONTAINING LEPIDOPTERAN INSECT PHEROMONES

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Paragraph 0198; 0199, (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.

Stereodirectional synthesis of the main component of pheromone (9Z,12E)-tetradeca-9,12-dienyl acetate by cross-coupling

Matveeva,Erin,Leshcheva,Kurts

, p. 765 - 770 (2007/10/03)

By cross-coupling of alkynyl cuprate with crotyl halides was synthesized (9Z,12E)-tetradeca-9-12-dienyl acetate, the main component of pheromones of several insect species Lepidoptera. The assignment of the chemical shifts of diene system was performed by 1H and 13NMR spectroscopy.

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