68892-13-7

Usage

Uses

Used in Pharmaceutical Industry:
1-Phenyldecane-1,3-dione is used as an organic intermediate compound for the synthesis of various pharmaceutical products. Its unique chemical structure allows it to participate in multiple chemical reactions, making it a valuable component in the development of new drugs and medications.
Used in Chemical Research:
1-Phenyldecane-1,3-dione is employed as a research compound in various chemical studies. Its versatile chemical properties enable researchers to explore its potential applications and interactions with other compounds, furthering the understanding of its role in chemical reactions and processes.
Used in Organic Synthesis:
1-Phenyldecane-1,3-dione is used as a key component in organic synthesis, where it can be transformed into a variety of other compounds through different chemical reactions. Its presence in the synthesis process can lead to the creation of new organic molecules with potential applications in various industries.

InChI:InChI=1/C16H22O2/c1-2-3-4-5-9-12-15(17)13-16(18)14-10-7-6-8-11-14/h6-8,10-11H,2-5,9,12-13H2,1H3

Upstream product

• 106-32-1 octanoic acid ethyl ester 
• 98-86-2 acetophenone 
• 638-45-9 1-Iodohexane 
• 93-91-4 1-phenylbutan-1,3-dione 
• 13283-92-6 β-ketodecanoic acid 
• 6756-74-7 S-benzoyl coenzyme A 
• 524-14-1 S-(hydrogen malonyl)coenzyme A 
• 111-11-5 methyl octanate 
• 1341177-73-8 β-ketodecanoyl-N-acetylcysteamine thioester 
• 50411-91-1 β-ketodecanoyl-CoA 

Relevant academic research and scientific papers

Synthesis of Unnatural 2-Substituted Quinolones and 1,3-Diketones by a Member of Type III Polyketide Synthases from Huperzia serrata

A curcuminoids, benzalacetone-, and quinolone-producing type III polyketide synthase (HsPKS3) from Huperzia serrata uniquely catalyzes the formation of unnatural 2-substituted quinolones and 1,3-diketones via head-to-head condensation of two completely different substrates. The broad range of substrate tolerance of HsPKS3 facilitates accessing structurally diverse 2-substituted quinolones and 1,3-diketones.

METHOD FOR SYNTHESIZING BETA-DICARBONYL COMPOUNDS

A method for synthesizing beta-dicarbonyl compounds, particularly beta-diketones, from at least two carbonyl compounds, such as esters and ketones, in the presence of a strong base or a mixture of strong bases by Claisen condensation with a titer of greater than 95%. The method includes providing a synthesis reactor on which a separation column, provided with a condenser and with at least one microwave generator, is mounted; feeding a first carbonyl compound and the strong base into the synthesis reactor; heating the reactor and starting up the condenser; starting up the microwave generator(s); when the mixture is brought to a boil at total flux, feeding the second carbonyl compound into the reactor; and after a waiting time, stopping the reactor and acidifying and washing the reaction mixture.)

Substituted oxazoles and thiazoles derivatives as hPPARγ and hPPARα activators

The present invention discloses compounds of formula (I), and tautomeric forms, pharmaceutically acceptable salts, or solvates thereof. Preferably, the compounds of the invention are dual activators of hPPARγ and hPPAR{acute over (α)}.

Process for base-promoted condensation reactions and base reagent therefor

A method for the preparation of 1,3-diketones is disclosed wherein the method comprises the steps of:(A) mixing an alkali metal base with a hindered alcohol in an aromatic hydrocarbon solvent;(B) boiling the mixture and azeotropically distilling water formed by the reaction between the base and the alcohol, whereby a solution of a hindered alkali metal alkoxide is formed in situ in the solvent;(C) mixing an ester with the solution of the hindered alkali metal alkoxide in the aromatic hydrocarbon solvent; and then(D) adding a ketone to the mixture.