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(3Z,5Z)-16,16-Diethoxy-3,5-hexadecadiene is a chemical compound with the molecular formula C20H38O2. It is a diene, meaning it contains two double bonds, which are both in the Z configuration. The diethoxy group consists of two ethoxy (?O?CH2CH3) functional groups attached to the 16th carbon atom on the molecule. (3Z,5Z)-16,16-Diethoxy-3,5-hexadecadiene is commonly used in organic synthesis and chemical research as a precursor to various other compounds. It has potential applications in the development of pharmaceuticals, agrochemicals, and materials. Additionally, it is important to handle this chemical with care due to its potential flammability and irritant properties.

71673-23-9

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71673-23-9 Usage

Uses

Used in Organic Synthesis:
(3Z,5Z)-16,16-Diethoxy-3,5-hexadecadiene is used as a precursor in organic synthesis for the production of various other compounds. Its unique structure with two double bonds in the Z configuration allows for versatile chemical reactions and the creation of a wide range of molecules.
Used in Chemical Research:
(3Z,5Z)-16,16-Diethoxy-3,5-hexadecadiene is also utilized in chemical research to study the properties and reactivity of dienes and their functional groups. Understanding the behavior of (3Z,5Z)-16,16-Diethoxy-3,5-hexadecadiene can contribute to the development of new synthetic methods and the discovery of novel chemical reactions.
Used in Pharmaceutical Development:
(3Z,5Z)-16,16-Diethoxy-3,5-hexadecadiene is used as a starting material in the development of pharmaceuticals. Its potential to be transformed into various other compounds makes it a valuable asset in the creation of new drugs with specific therapeutic properties.
Used in Agrochemical Development:
In the agrochemical industry, (3Z,5Z)-16,16-Diethoxy-3,5-hexadecadiene is used as a precursor for the synthesis of various agrochemicals, such as pesticides and herbicides. Its versatility in organic synthesis allows for the development of targeted and effective products for agricultural use.
Used in Material Development:
(3Z,5Z)-16,16-Diethoxy-3,5-hexadecadiene is also used in the development of new materials, where its unique structure and properties can be exploited to create materials with specific characteristics, such as improved strength, flexibility, or chemical resistance.
Safety Precautions:
Due to its potential flammability and irritant properties, (3Z,5Z)-16,16-Diethoxy-3,5-hexadecadiene should be handled with care, following proper safety protocols and guidelines to minimize risks during its use in various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 71673-23-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,6,7 and 3 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 71673-23:
(7*7)+(6*1)+(5*6)+(4*7)+(3*3)+(2*2)+(1*3)=129
129 % 10 = 9
So 71673-23-9 is a valid CAS Registry Number.
InChI:InChI=1/C20H38O2/c1-4-7-8-9-10-11-12-13-14-15-16-17-18-19-20(21-5-2)22-6-3/h7-10,20H,4-6,11-19H2,1-3H3/b8-7+,10-9+

71673-23-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (11Z,13Z)-1,1-diethoxy-11,13-hexadecadiene

1.2 Other means of identification

Product number -
Other names (Z,Z)-11,13-Hexadecadienal Diethyl Acetal

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:71673-23-9 SDS

71673-23-9Relevant academic research and scientific papers

New synthesis of (11Z,13Z)-11,13-Hexadecadienal, the female sex pheromone of the navel orangeworm

Mori, Kenji

experimental part, p. 2727 - 2730 (2010/09/11)

(11Z,13Z)-11,13-Hexadecadienal, the female sex pheromone of the navel orangeworm (Amyelois transitella), was synthesized from commercially available 10-bromo-1-decanol in a 27% overall yield (8 steps). The synthesis was achieved by using 10-iododecanal, trimethylsilylacetylene and (Z)-1-bromo-12-butene as the key building blocks, employing Sonogashira-Hagihara coupling and Brown's hydroboration-protonolysis as the key reactions. The terminal formyl group was installed in the earlier stage of the synthesis rather than in the final step. This procedure enabled the multi-gram-scale preparation of this economically important pheromone.

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