2345-12-2

Usage

Molecular structure

A 12-carbon chain with a ketone group at the third position.

Origin

Commonly found in various natural sources, including plant oils and animal fats.

Potential applications

In the food industry as a flavoring agent, and in the cosmetic industry as an ingredient in skin and hair care products.

Antimicrobial properties

Studies have shown that 12-oxotridecanoic acid may have antimicrobial properties.

Antioxidant properties

Studies have shown that 12-oxotridecanoic acid may have antioxidant properties.

Therapeutic and pharmaceutical applications

The antimicrobial and antioxidant properties make it of interest for potential therapeutic and pharmaceutical applications.

Diverse range of potential uses and properties

12-oxotridecanoic acid is an interesting compound for further research and development.

InChI:InChI=1/C13H24O3/c1-12(14)10-8-6-4-2-3-5-7-9-11-13(15)16/h2-11H2,1H3,(H,15,16)

Upstream product

• 99706-68-0 tridecane-1,12-diol 
• 112-38-9 10-undecenoic acid 
• 75-07-0 acetaldehyde 
• 32400-12-7 Cyclododecanoncarboxaldehydtosylhydrazon 
• 73125-64-1 12-oxotridecanal 
• 1892-12-2 hydroxymethylcyclododecane 
• 5037-22-9 formyl cyclododecane 
• 5009-33-6 1-dodecen-11-one 
• 124-38-9 carbon dioxide 
• 830-13-7 cyclododecanone 
• 32400-07-0 methylenecyclodecane 
• 16339-75-6 12-tridecenyl alcohol 
• 858846-07-8 1,12-dibromo-tridecane 

Downstream Products

• 56247-70-2 20-Oxoheneicosansaeuremethylester 

Relevant academic research and scientific papers

INSECT PHEROMONES AND THEIR ANALOGUES XXXVI. SYNTHESIS OF 13-HYDROXY-2-OXOTRIDECANE - AN ATTACTANT OF THE HONEYBEE

A six-stage synthesis of 13-hydroxy-2-oxotridecane - a sex attractant of the honeybee - has been achieved with the use of ozonolysis as the key stage.

Site-Selective Catalytic Carboxylation of Unsaturated Hydrocarbons with CO2 and Water

A catalytic protocol that reliably predicts and controls the site-selective incorporation of CO2 to a wide range of unsaturated hydrocarbons utilizing water as formal hydride source is described. This platform unlocks an opportunity to catalytically repurpose three abundant, orthogonal feedstocks under mild conditions.

Alkylaluminium Dichloride Induced Friedel-Crafts Acylation of Unsaturated Carboxylic Acids and Alcohols

The ethylaluminium dichloride induced Friedel-Crafts acylation of unsaturated carboxylic acids, for example 10-undecenoic acid (1a) and oleic acid (5a), and of the respective alcohols 1b and 5b with acyl chlorides and cyclic acyl anhydrides gave the corresponding long-chain β,γ-unsaturated ketones 3, 6/7, 11 and 13/14 with ω-carboxy and ω-hydroxy functions, respectively.The intramolecular cyclization of petroselinic acid chloride (17) yielded (E)-2-dodecylidenecyclohexanone (18).Catalytic hydrogenation gave the respective saturated ketones 4, 8/9, 12, 15/16 and 19.Key Words: Friedel-Crafts acylation / β,γ-Unsaturated keto carboxylic acids and alcohols

Indirect Electrooxidation of Alkohols and Aldehydes by Using a Double Mediatory System Consisting of RuO4/RuO2 and Cl+/Cl- Redoxes in an Aqueous-Organic Two-Phase System

A double mediatory system consisting of RuO4/RuO2 and Cl+/Cl- redox couples has been developed for the indirect electrooxidation of alcohols and aldehydes.The reaction proceeds in the following manner: (1) oxidation of the substrate with ruthenium tetraoxide (RuO4) in the organic layer, (2) regeneration of ruthenium tetraoxide from ruthenium dioxide (RuO2) with active chlorine species (Cl2 or +), and (3) oxidation of chloride ion to + on the anode in the aqueous layer.The range of applicability of the present procedure is discussed by oxidations of (1)secondary alcohols to ketones, (2) primary alcohols and aldehydes to carboxylic acid, (3) 1,n-diols to lactones and keto acids, and (4) carbohydrate derivatives.