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24738-49-6

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24738-49-6 Usage

Description

2,4-Tetradecadienoic acid, (E,E)is a diunsaturated fatty acid with a double bond at the 2nd and 4th carbon atoms. It is an organic compound that plays a significant role in various chemical and industrial processes due to its unique structure and properties.

Uses

Used in Polymerization Reactions:
2,4-Tetradecadienoic acid, (E,E)is used as a reactant in polymerization reactions for the synthesis of monoacylglycerol and 1,2-diacyl-sn-glycerol. Its presence in these reactions contributes to the formation of complex polymers with specific properties and applications in various industries.
Used in Chemical Industry:
In the chemical industry, 2,4-Tetradecadienoic acid, (E,E)is utilized as an intermediate in the production of various chemicals and compounds. Its unique structure allows it to participate in multiple chemical reactions, making it a valuable component in the synthesis of a wide range of products.
Used in Pharmaceutical Industry:
2,4-Tetradecadienoic acid, (E,E)may also find applications in the pharmaceutical industry, where it can be used as a building block for the development of new drugs or as a component in drug formulations. Its versatility and reactivity make it a promising candidate for various medicinal applications.
Used in Cosmetics Industry:
In the cosmetics industry, 2,4-Tetradecadienoic acid, (E,E)can be used as an ingredient in various cosmetic products. Its properties may contribute to the development of innovative formulations with improved performance and benefits for consumers.
Used in Food Industry:
2,4-Tetradecadienoic acid, (E,E)may also have applications in the food industry, where it can be used as an additive or component in the production of food products. Its unique properties may enhance the taste, texture, or shelf life of various food items.

Check Digit Verification of cas no

The CAS Registry Mumber 24738-49-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,7,3 and 8 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 24738-49:
(7*2)+(6*4)+(5*7)+(4*3)+(3*8)+(2*4)+(1*9)=126
126 % 10 = 6
So 24738-49-6 is a valid CAS Registry Number.

24738-49-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-(E,E)-tetradecadienoic acid

1.2 Other means of identification

Product number -
Other names (2E,4E)-tetradecadienoic acid

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:24738-49-6 SDS

24738-49-6Relevant articles and documents

Synthesis of Bungeanool, Isobungeanool, Dihydrobungeanool, Tetrahydrobungeanool, Hazaleamide, Lanyuamide III, and Analogues

Loo, Ying-Hui,Leakasindhu, Suleeporn,Kan, Chi-Ming,Toy, Patrick H.

, p. 1145 - 1156 (2021/11/09)

The bungeanools are a family of alkamide natural products isolated from the pericarps of Zanthoxylum bungeanum (Sichuan pepper), and they are structurally related to the sanshools. While the sanshools, especially hydroxy-?-sanshool, have been studied in a variety of contexts, research regarding the bungeanools has been much more limited. To facilitate their study, we have developed stereoselective syntheses of all four members of this family of compounds by using flexible routes that are also amenable to the synthesis of analogues. The key transformation in the syntheses was the stereoselective triphenylphosphine/ phenol-catalyzed isomerization of an alkynoate to the corresponding conjugated E,E-dienoate.

Synthesis of the fatty acid of pramanicin

Cow, Christopher,Valentini, David,Harrison, Paul

, p. 884 - 889 (2007/10/03)

The natural product tetradec-2-enoic acid-4,5-epoxide (2), which is also a component of the antibiotic pramanicin (1), was prepared in racemic form by a glycoluril-template directed approach. Two sequential additions of acetate units to decanoic acid are

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