15266-35-0

Usage

Uses

Used in Pest Control Applications:
1-Methyl-2-tridecylquinolin-4(1H)-one is used as an avicide and rodenticide for the purpose of managing and reducing pest bird and rodent populations that can cause damage to crops, property, and spread diseases. Its application is particularly valuable in agricultural settings where it helps protect crops from being destroyed by pests.
Used in Agricultural Industry:
In the agricultural industry, 1-Methyl-2-tridecylquinolin-4(1H)-one is used as a pest control agent to safeguard crops from the detrimental effects of pest birds and rodents. It is applied to control the populations that can lead to significant economic losses if left unchecked.
Used in Urban Settings:
1-Methyl-2-tridecylquinolin-4(1H)-one is also used in urban settings as a rodenticide to manage rodent infestations that can lead to health hazards and property damage. Its application helps in maintaining cleanliness and reducing the risk of disease transmission.
Regulatory Considerations:
Due to the potential hazards associated with 1-Methyl-2-tridecylquinolin-4(1H)-one, its use is regulated and restricted in many countries. It is typically applied in the form of bait or a liquid concentrate, and strict adherence to safety measures is required to minimize the impact on non-target species and the environment.

Upstream product

• 2345-28-0 pentadecan-2-one 
• 10328-92-4 N-Methylisatoic anhydride 
• 693-02-7 hex-1-yne 
• 83-54-5 1-methyl-4-quinolone 
• 2437-56-1 1-tridecene 
• 17814-85-6 (4-carboxybutyl)triphenylphosphonium bromide 
• 5684-70-8 (Z)-tetradec-5-enoic acid 
• 2067-33-6 5-bromopentanoic acid 
• 250293-82-4 1-methyl-2-[(Z)-4'-tridecenyl]-4(1H)-quinolone 
• 98321-50-7 1-methyl-2-(8-tridecynyl)-4(1H)-quinolinone 
• 98321-46-1 10-pentadecyn-2-one 
• 55182-92-8 9-tetradecynoic acid 
• 17696-11-6 8-bromooctanoic acid 
• 15266-38-3 evocarpine 

Relevant academic research and scientific papers

Quinolone alkaloids from Evodia rutaecarpa

Five new quinolone alkaloids were isolated from the fruits of Evodia rutaecarpa, together with seven known ones. Their structures were determined on the basis of spectral data and chemical reactions.

Alkylation of pyridone derivatives by nickel/Lewis acid catalysis

MAD as an additive: The [Ni(cod)2], (2,6-tBu2-4- MeC6H2O)2AlMe (MAD), and N-heterocyclic carbene (NHC) catalytic system effected a highly regioselective alkylation of pyridone derivatives (see scheme). Substituted pyridones and related heterocycles react with both terminal and internal alkenes to selectively give a range of nitrogen-containing heterocycles with linear alkyl substituents. Copyright

Design, synthesis and antimycobacterial activities of 1-methyl-2-alkenyl- 4(1H)-quinolones

A series of 23 new 1-methyl-2-alkenyl-4(1H)quinolones have been synthesized and evaluated in vitro for their antimycobacterial activities against fast growing species of mycobacteria, such as Mycobacterium fortuitum, M. smegmatis and M. phlei. The compounds displayed good to excellent inhibition of the growth of the mycobacterial test strains with improved antimycobacterial activity compared to the hit compound, evocarpine. The most active compounds, which possessed chain length of 11-13 carbons at position-2 displayed potent inhibitory effects with an MIC value of 1.0 mg/L. In a human diploid embryonic lung cell line, MRC-5 cytotoxicity assay, the alkaloids showed weak to moderate cytotoxic activity. Biological evaluation of these evocarpine analogues on the less pathogenic fast growing strains of mycobacteria showed an interesting antimycobacterial profile and provided significant insight into the structure-activity relationships.

The Chemistry of 2H-3,1-Benzoxazine-2,4(1H)-dione (Isatoic Anhydride). 17. Synthesis of 2-Alkyl-4-quinolone Alkaloids via a One-step Reaction of N-Methylisatoic Anhydride with Methyl Ketone Enolates

Lithium enolates derived from aliphatic methyl ketones react with N-methylisatoic anhydride (5) at -78 deg C to give 2-alkyl-4-quinolone alkaloids 7 in a single step.The method was used to synthesize both double bond isomers of 1-methyl-2-(8-tridecenyl)-4(1H)-quinolinone (8) thereby showing that the alkaloid evocarpine possesses the Z-olefin stereochemistry 8a.Reduction of 8a provided the alkaloid dihydroevocarpine (16).Compound 16 was also directly prepared from the reaction of 5 with the lithium enolate of 2-pentadecanone.