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57818-41-4

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57818-41-4 Usage

Description

3,4-DiMethyl-5-propyl-2-furanundecanoic Acid, also known as F4 furan fatty acid, is a type of furan fatty acid that is predominantly found in algae and fish, although it is also produced by plants and microorganisms. 3,4-DiMethyl-5-propyl-2-furanundecanoic Acid is characterized by its radical-scavenging ability and anti-inflammatory properties, making it a potential candidate for various applications in different industries.

Uses

Used in Pharmaceutical Industry:
3,4-DiMethyl-5-propyl-2-furanundecanoic Acid is used as a therapeutic agent for its anti-inflammatory properties, which can help in the treatment of various inflammation-related conditions. Its radical-scavenging ability also suggests potential applications in the development of treatments for oxidative stress-related diseases.
Used in Nutraceutical Industry:
In the nutraceutical industry, 3,4-DiMethyl-5-propyl-2-furanundecanoic Acid is used as a functional ingredient due to its health-promoting and disease-preventing properties. Its presence in algae and fish makes it a valuable component in the development of supplements and fortified foods targeting inflammation and oxidative stress.
Used in Cosmetics Industry:
3,4-DiMethyl-5-propyl-2-furanundecanoic Acid is used as an active ingredient in the cosmetics industry, where its anti-inflammatory and radical-scavenging properties can be harnessed to develop products aimed at improving skin health and reducing signs of aging or inflammation.
Used in Agricultural Industry:
In agriculture, 3,4-DiMethyl-5-propyl-2-furanundecanoic Acid can be used as a natural additive to enhance the nutritional value of animal feed, particularly for fish and other aquatic species, due to its presence in their natural diet and its beneficial properties.
Overall, 3,4-DiMethyl-5-propyl-2-furanundecanoic Acid, with its unique properties, has the potential to be utilized across various industries, offering a range of applications from pharmaceuticals to cosmetics and agriculture.

Check Digit Verification of cas no

The CAS Registry Mumber 57818-41-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,8,1 and 8 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 57818-41:
(7*5)+(6*7)+(5*8)+(4*1)+(3*8)+(2*4)+(1*1)=154
154 % 10 = 4
So 57818-41-4 is a valid CAS Registry Number.

57818-41-4SDS

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 11-(3,4-dimethyl-5-propylfuran-2-yl)undecanoic acid

1.2 Other means of identification

Product number -
Other names 2-Furanundecanoic acid,3,4-dimethyl-5-propyl

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:57818-41-4 SDS

57818-41-4Downstream Products

57818-41-4Relevant articles and documents

A General Convergent Strategy for the Synthesis of Tetra-Substituted Furan Fatty Acids (FuFAs)

Wang, Yamin,Pritchard, Gareth J.,Kimber, Marc C.

, p. 2914 - 2922 (2020/03/26)

Using a palladium catalyzed - acid mediated isomerization sequence, tetrasubstituted furans suitable for furan fatty acid (FuFA) total synthesis can be effectively constructed in high yield. This convergent approach installs the essential carbon side chains at the α1- and α2 -positions, the β1-methyl group, and importantly, an electron withdrawing group at the β2-position tempering the reactivity of the electron rich furan in the FuFAs. When this EWG is an ester, it was conveniently transformed into the required β1-methyl group in three high yielding synthetic steps. Using this approach, the total synthesis of 11D5 and 11D3 was accomplished in 7-steps from commercially available starting materials in overall yields of 52 % and 48 %, respectively. Furthermore, this methodology also provided an efficient synthetic route to the decarboxy analogues of both 11D5 and 11D3.

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