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9,12-Tetradecadien-1-ol, acetate, (E,E)is an organic compound that belongs to the class of acetates. It is characterized by the presence of two double bonds in the E,E configuration, which gives it unique chemical properties and potential applications in various fields.

70654-47-6

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70654-47-6 Usage

Uses

Used in Agricultural Industry:
9,12-Tetradecadien-1-ol, acetate, (E,E)is used as an agricultural compound for controlling insects. Its insecticidal properties make it a valuable tool in pest management strategies, helping to protect crops and reduce the need for chemical pesticides.
Used in Chemical Synthesis:
9,12-Tetradecadien-1-ol, acetate, (E,E)is also used in the preparation of insect pheromones. This is achieved through a Z-selective cross metathesis reaction using a ruthenium catalyst. This method allows for the efficient synthesis of insect pheromones, which can be used in pest control and monitoring programs to attract and trap target insect species.

Check Digit Verification of cas no

The CAS Registry Mumber 70654-47-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,6,5 and 4 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 70654-47:
(7*7)+(6*0)+(5*6)+(4*5)+(3*4)+(2*4)+(1*7)=126
126 % 10 = 6
So 70654-47-6 is a valid CAS Registry Number.

70654-47-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (9E,12E)-tetradeca-9,12-dien-1-yl acetate

1.2 Other means of identification

Product number -
Other names (9E,12E)-9,12-tetradecadienyl acetate

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:70654-47-6 SDS

70654-47-6Downstream Products

70654-47-6Relevant academic research and scientific papers

SYNTHESIS OF Z-OLEFIN-CONTAINING LEPIDOPTERAN INSECT PHEROMONES

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Paragraph 0200; 0201, (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.

Facile synthesis of mill moth's sex pheromone components

Hornyanszky, Gabor,Rohaly, Janos,Novak, Lajos

, p. 1533 - 1540 (2008/09/20)

An improved method for the preparation of mill moth's sex pheromone components in high diastereomeric purity is described. Copyright Taylor & Francis Group, LLC.

Pheromones, XXXV. - Stereoselective Syntheses of 1,4-Alkadienes

Bestmann, Hans Juergen,Koschatzky, Karl-Heinrich,Plenchette, Alain,Suess, Joachim,Vostrowsky, Otto

, p. 536 - 544 (2007/10/02)

The stereoselective synthesis of 1,4-alkadienes via Julia synthesis, Wittig reaction, Crombie synthesis and methylene interruption of conjugated alkadienylphosphonates is described.

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