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.
Check Digit Verification of cas no
The CAS Registry Mumber 2345-12-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,4 and 5 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2345-12:
(6*2)+(5*3)+(4*4)+(3*5)+(2*1)+(1*2)=62
62 % 10 = 2
So 2345-12-2 is a valid CAS Registry Number.
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)
2345-12-2Relevant articles and documents
INSECT PHEROMONES AND THEIR ANALOGUES XXXVI. SYNTHESIS OF 13-HYDROXY-2-OXOTRIDECANE - AN ATTACTANT OF THE HONEYBEE
Odinokov, V. N.,Ishmuratov, G. Yu.,Ladenkova, I. M.,Tolstikov, G. A.
, p. 235 - 236 (1992)
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.
Alkylaluminium Dichloride Induced Friedel-Crafts Acylation of Unsaturated Carboxylic Acids and Alcohols
Metzger, Juergen O.,Biermann, Ursula
, p. 645 - 650 (2007/10/02)
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
