493-45-8

Usage

Uses

Used in Pharmaceutical Industry:
(2S)-Tetrahydro-4β-methyl-5-oxo-2-tridecyl-3β-furancarboxylic acid is used as a pharmaceutical agent for its potential role in lipid metabolism regulation and other physiological processes. Its unique stereochemistry and molecular structure may offer specific therapeutic benefits, making it a candidate for the development of new drugs targeting various health conditions.
Used in Biochemical Research:
In the field of biochemical research, (2S)-Tetrahydro-4β-methyl-5-oxo-2-tridecyl-3β-furancarboxylic acid serves as a valuable compound for studying the effects of chirality and molecular structure on biological activity. Its properties can be explored to understand better how similar compounds interact with biological systems and contribute to various physiological functions.
Used in Cosmetics Industry:
(2S)-Tetrahydro-4β-methyl-5-oxo-2-tridecyl-3β-furancarboxylic acid is used as an ingredient in cosmetics for its potential benefits to skin health. Its fatty acid derivative nature may provide moisturizing and nourishing effects, contributing to the development of skincare products that promote healthy and hydrated skin.
Used in Food Industry:
In the food industry, (2S)-Tetrahydro-4β-methyl-5-oxo-2-tridecyl-3β-furancarboxylic acid may be utilized as a component in the development of functional foods or supplements. Its potential impact on lipid metabolism could be harnessed to create products that support heart health or weight management.

Upstream product

• 493-46-9 tetrahydro-4-methylene-5-oxo-2-tridecyl-3-furancarboxylic acid 
• 220344-53-6 tert-butyl-(4-chloro-1-tridecyl-but-2-ynyloxy)-dimethyl-silane 
• 220344-52-5 1-chloro-heptadec-2-yn-4-ol 
• 124-25-4 myristylaldehyde 
• 22800-27-7 (-)-allo-protolichesterinic acid 

Relevant academic research and scientific papers

Vicinal dianion of triethyl ethanetricarboxylate: Syntheses of (±)-lichesterinic acid, (±)-phaseolinic acid, (±)-nephromopsinic acid, (±)-rocellaric acid, and (±)-dihydroprotolichesterinic acid

The vicinal dianion 2 derived from triethyl ethanetricarboxylate reacted regioselectively with aldehydes and ketones at C(β) to provide paraconic acid derivatives 5a-f in moderate to high yields as mixtures of diastereoisomers. The paraconic acid derivatives 5e and 5f were utilized as the starting materials for the syntheses of (±)-lichesterinic acid (12), (±)-phaseolinic acid (13), (±)-nephromopsinic acid (14), (±)-rocellaric acid (15), and (±)-dihydroprotolichesterinic acid (16).

Total synthesis of (±)-dihydroprotolichesterinic acid and formal synthesis of (±)-Roccellaric acid by radical cyclisation of an epoxide. Using a transition-metal radical source

A short and efficient total synthesis of (±)-Dihydroprotolichesterinic acid (1) and Formal synthesis of (±)-Roccellaric acid (2) has been achieved by radical cyclisation of epoxide using a transition metal radical source.

Efficient total syntheses of (±)protolichesterinic acid and (±)rocellaric acid via tungsten-π-allyl complexes

Total syntheses of racemic protolichesterinic acid (1) and rocellaric acid (2) were achieved with the use of tungsten-π-allyl complex in the key step. In this synthetic route, compounds 1 and 2 were prepared in four and six steps respectively starting from readily available chloropropargyl derivatives.

Contribution to the Chemistry of Proto- and allo-Proto-lichesterinic Acids

The isolation and spectroscopic characterization of (-)-allo-proto-lichesterinic acid from Cetraria komarovii is described.Proto-lichesterinic and allo-proto-lichesterinic acids are transformed into numerous nitrogen-containing derivatives and the isomerization of the dihydro acids is investigated. Key words: Proto-lichesterinic Acid, allo-Proto-lichesterinic Acid, Lichen Substances