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18409-20-6

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18409-20-6 Usage

Description

2,4-OCTADIEN-1-OL, also known as (2E,4E)-2,4-Octadien-1-ol, is a chemical compound with a mild, pleasant, fatty odor. It is characterized by its fatty, oily, and waxy taste with a savory chicken and beef note, along with a creamy cucumber and melon nuance. 2,4-OCTADIEN-1-OL is known for its unique chemical properties and various applications across different industries.

Uses

Used in Pheromone Synthesis:
2,4-OCTADIEN-1-OL is used as a useful intermediate in the synthesis of sex pheromone components for sphingid moths and other sex attractants. Its role in pheromone synthesis is crucial for studying and controlling insect populations, particularly in agricultural and ecological settings.
Used in Flavor and Fragrance Industry:
2,4-OCTADIEN-1-OL is used as a flavoring agent for its fatty, oily, and waxy taste characteristics, with a savory chicken and beef note, and a creamy cucumber and melon nuance. It is particularly useful in the creation of flavors for the food and beverage industry.
Used in Aroma Industry:
2,4-OCTADIEN-1-OL is used as an aroma compound for its mild, pleasant, fatty odor. It is ideal for the fragrance industry, where it can be used to create various scent profiles for perfumes, cosmetics, and other scented products.

Check Digit Verification of cas no

The CAS Registry Mumber 18409-20-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,4,0 and 9 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 18409-20:
(7*1)+(6*8)+(5*4)+(4*0)+(3*9)+(2*2)+(1*0)=106
106 % 10 = 6
So 18409-20-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H14O/c1-2-3-4-5-6-7-8-9/h4-7,9H,2-3,8H2,1H3/b5-4+,7-6+

18409-20-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (2E,4E)-octa-2,4-dien-1-ol

1.2 Other means of identification

Product number -
Other names trans-2,4-octadien-1-ol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Flavouring Agent: FLAVOURING_AGENT
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:18409-20-6 SDS

18409-20-6Relevant articles and documents

Cobalt-Catalyzed Diastereo- And Enantioselective Reductive Allyl Additions to Aldehydes with Allylic Alcohol Derivatives via Allyl Radical Intermediates

Wang, Lei,Wang, Lifan,Li, Mingxia,Chong, Qinglei,Meng, Fanke

, p. 12755 - 12765 (2021/08/30)

Catalytic generation of ambiphilic π-allyl-metal complexes and their utility in enantioselective transformations constitutes a powerful approach for introduction of allyl groups to a molecule. Herein an unprecedented cobalt-catalyzed highly site-, diastereo-, and enantioselective protocol for stereoselective formation of nucleophilic allyl-Co(II) complexes followed by addition to aldehydes is presented. The reaction features diastereo- and enantioconvergent conversion of easily accessible allylic alcohol derivatives to diversified enantioenriched homoallylic alcohols with a remarkably broad scope of allyl groups that can be introduced. Mechanistic studies indicated that allyl radical intermediates were involved in this process. These new discoveries establish a new strategy for development of enantioselective transformations through capture of radicals by chiral Co complexes, pushing forward the frontier of Co complexes for enantioselective catalysis.

Cobalt-catalyzed versus uncatalyzed intramolecular Diels-Alder cycloadditions

Biletskyi, Bohdan,Tenaglia, Alphonse,Clavier, Hervé

supporting information, p. 103 - 107 (2017/12/28)

The intramolecular [4+2] cycloadditions of dienynes was investigated using cobalt-based catalysts. Substrates without substitution on alkyne moiety were found to react under thermal activation. The use of a cobalt salt as catalyst made reactions cleaner by limiting the formation of byproducts. Cycloadditions with dienynes possessing a substituent on the alkyne pattern occurred only in presence of a cobalt catalyst which displayed a moderate to good activity depending on the substrate patterns.

Aggregation behavior of tetraenoic fatty acids in aqueous solution

Wang, Yonghui,Ma, Jianguo,Cheon, Hwan-Sung,Kishi, Yoshito

, p. 1333 - 1336 (2008/04/05)

(Chemical Equation Presented) Why so blue? Unique blue-shifted UV absorptions were used to follow the aggregation of C24 tetraene fatty acids in aqueous solution. Aggregation takes place through three distinct states (i.e. K→T1→T2; see picture). It is suggested that all of these aggregates are lamellar-type in a local sense but differ in the packing mode of the fatty acid backbone.

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