60437-21-0

Basic information

• Product Name: 12-Tridecen-2-one
• Synonyms: 12-Tridecen-2-one
• CAS NO: 60437-21-0
• Molecular Formula: C₁₃H₂₄O
• Molecular Weight: 196.33
• Mol File: 60437-21-0.mol
• Article Data: 7

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 12-Tridecen-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: 12-Tridecen-2-one(60437-21-0)
• EPA Substance Registry System: 12-Tridecen-2-one(60437-21-0)

Safety Data

• Hazardous Substances Data: 60437-21-0(Hazardous Substances Data)

Usage

Occurrence

Naturally occurring chemical compound found in many plants and essential oils

Production

Pheromone produced by insects

Role

Floral scent in some flowers

Use in fragrance industry

Used as a perfume ingredient due to its sweet, floral, and woody aroma

Medicinal properties

Being studied for its potential anti-inflammatory, antioxidant, and anti-cancer effects

Therapeutic potential

Demonstrated potential as a therapeutic agent in the treatment of various health conditions, making it an interesting compound for further research and development.

Upstream product

• 2389-02-8 13-oxotetradecanoic acid 
• 7766-50-9 1-undecen-11-ylbromide 
• 18815-73-1 methylzinc iodide 
• 917-64-6 methyl magnesium iodide 
• 36218-86-7 11-oxododecanal 
• 31729-70-1 bis(iodozinc)methane 
• 92605-43-1 tridec-1-en-12-yne 
• 74-85-1 ethene 
• 67-64-1 acetone 
• 96562-66-2 tridec-12-en-2-ol 
• 832-10-0 cyclotridecanone 
• 84465-81-6 dodec-11-enoyl chloride 
• 7766-49-6 1-iodo-10-undecene 

Downstream Products

• 59812-98-5 tridecan-2-ol 
• 593-08-8 tridecan-2-one 

Relevant articles and documents

PALLADIUM-CATALYZED DECARBONYLATION OF FATTY ACID ANHYDRIDES FOR THE PRODUCTION OF LINEAR ALPHA OLEFINS

The present invention is directed to methods of forming olefins, especially linear alpha olefins from fatty acids or anhydrides, each method comprising: contacting an amount of precursor carboxylic acid anhydride with a palladium catalyst comprising a bidentate bis-phosphine ligand in a reaction mixture so as to form an olefin in a product with the concomittant formation and removal of CO and water from the reaction mixture, either directly or indirectly, wherein the reaction mixture is maintained with a sub-stoichiometric excess of a sacrificial carboxylic acid anhydride, an organic acid, or both, said sub-stoichiometric excess being relative to the amount of the precursor carboxylic acid anhydride. The precursor carboxylic acid anhydride may be added to the reaction mixture directly or formed in situ by the reaction between at least one precursor carboxylic acid with a stoichiometric amount of the sacrificial acid anhydride.

Alkylidenation of carbonyl compounds with gem-dizincioalkanes mediated with titanium dichloride

Olefination of carbonyl compounds with gem-dizincio-alkanes, bis(iodozincio)methane, 1,1-bis(iodozincio)ethane, and bis(bromozincio)methyltrimethylsilane, afforded the corresponding olefins in good to excellent yields.

Photochemistry of macrocyclic ketones within zeolites: Competition between norrish type I and type II reactivity

Photolysis of macrocyclic mono- and diketones (1 and 2) included in X and Y zeolites gives Norrish type I products in addition to the products obtained via the Norrish type II process, the only observed process in isotropic media. Enhancement of the type I over the type II process is cationdependent and especially large enhancements are obtained with Li and Na as cations. The zeolite effect is attributed to a reduction in the rate of the Norrish type II α-hydrogen abstraction process.