57818-37-8 Usage
Description
3-Methyl-5-pentyl-2-furanundecanoic Acid, also known as F5 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-Methyl-5-pentyl-2-furanundecanoic Acid is characterized by its radical-scavenging ability and anti-inflammatory properties, making it a valuable substance for various applications.
Uses
Used in Pharmaceutical Industry:
3-Methyl-5-pentyl-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 contributes to its potential use in the development of medications targeting oxidative stress-related diseases.
Used in Nutraceutical Industry:
In the nutraceutical industry, 3-Methyl-5-pentyl-2-furanundecanoic Acid is utilized as an additive for its health-promoting benefits. Its presence in algae and fish makes it a natural and valuable component in the formulation of supplements and functional foods aimed at enhancing overall health and well-being.
Used in Cosmetic Industry:
3-Methyl-5-pentyl-2-furanundecanoic Acid is employed as an active ingredient in the cosmetic industry, where its anti-inflammatory and radical-scavenging properties can be harnessed for the development of skincare products. These products may help in reducing inflammation, promoting skin health, and protecting the skin from environmental stressors.
Used in Agricultural Industry:
In agriculture, 3-Methyl-5-pentyl-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. Its presence can contribute to the overall health and well-being of these animals, leading to improved growth and development.
Overall, 3-Methyl-5-pentyl-2-furanundecanoic Acid, with its diverse applications across various industries, holds significant potential in contributing to human, animal, and environmental health.
Check Digit Verification of cas no
The CAS Registry Mumber 57818-37-8 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, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 57818-37:
(7*5)+(6*7)+(5*8)+(4*1)+(3*8)+(2*3)+(1*7)=158
158 % 10 = 8
So 57818-37-8 is a valid CAS Registry Number.
57818-37-8Relevant articles and documents
Optimised total syntheses of the F-furan fatty acids F5 and F6 and some deuterated derivatives Dedicated, with the greatest respect, to the memory of Professor Alan R. Katritzky
Knight, David W.,Smith, Andrew W.T.
, p. 7436 - 7444 (2015/08/24)
Optimised syntheses of F5- and F6-furan fatty acids 2 and 3 are described in full. Key steps include furan formation from a single 3-alkyne-1,2-diol 6 using 5-endo-dig cyclisations triggered by silver(I) nitrate or iodine. Introducti
Catalytic isomerization of 1-alkynyl-2,3-epoxy alcohols to substituted furans: Succinct routes to furanoid fatty acids and difurylmethanes
Marson, Charles M.,Harper, Steven
, p. 9223 - 9231 (2007/10/03)
A versatile procedure for the preparation of synthetically valuable 2,5- disubstituted and 2,3,5-trisubstituted furans via mercury(II)-mediated isomerization of 1-alkynyl-2,3-epoxy alcohols is described. Mercury(II)- catalyzed isomerization of alkynyl epoxides 3a-k derived from cyclic α- alkynyl allylic alcohols furnishes 2,3,5-substituted furans bearing an aldehyde or keto group on the C-2 side chain. The reaction is used in a succinct and efficient synthesis of the furanoid fatty acid F5. In contrast, the mercury(II)-catalyzed reaction of a series of alkynyl epoxides 3m-p lacking ring fusion affords difurylmethanes 5, presumably by the dimerization of intermediate 2-(α hydroxyalkyl)furans 4.
Sequential Pd(0)-catalyzed reactions for the construction of multiple substituted furans. A short synthesis of the F5 furan fatty acid
Bach, Thorsten,Krueger, Lars
, p. 1729 - 1732 (2007/10/03)
4,5-Dibromofurfural (1) undergoes a regioselective Pd(0)-catalyzed C-C bond forming reaction at its C-5 position to yield corresponding furans 3. The second bromine substituent in C-4 position can be substituted by a methyl group in a subsequent Pd(0)-catalyzed cross coupling reaction. The furan fatty acid 12 and its benzyl ester 13 were prepared in a short synthetic sequence using this method.
