5456-14-4

Usage

Uses

Used in Flavoring Industry:
Diethyl 2,6-dimethyl-4-oxo-pyran-3,5-dicarboxylate is used as a flavoring ingredient for its fruity and sweet aroma, enhancing the taste and smell of food and beverages.
Used in Fragrance Industry:
In the production of perfumes and other fragrance products, diethyl 2,6-dimethyl-4-oxo-pyran-3,5-dicarboxylate is utilized to contribute to the complex scent profiles of these products.
Used in Pharmaceutical Synthesis:
Diethyl 2,6-dimethyl-4-oxo-pyran-3,5-dicarboxylate serves as a building block in the synthesis of pharmaceuticals, playing a crucial role in the development of new medications.
Used in Organic Chemistry Research:
As a component in various organic reactions, diethyl 2,6-dimethyl-4-oxo-pyran-3,5-dicarboxylate is used in laboratory settings to facilitate scientific research and the discovery of new chemical compounds.
It is important to handle diethyl 2,6-dimethyl-4-oxo-pyran-3,5-dicarboxylate with care due to its potential to cause skin and eye irritation with prolonged exposure.

InChI:InChI=1/C13H16O6/c1-5-17-12(15)9-7(3)19-8(4)10(11(9)14)13(16)18-6-2/h5-6H2,1-4H3

Upstream product

• 108-24-7 acetic anhydride 
• 75-36-5 acetyl chloride 
• 105-50-0 diethyl 1,3-acetonedicarboxylate 
• 64-19-7 acetic acid 
• 129812-44-8 2,6-(Dibrommethyl)-4-oxo-4H-pyran-3,5-dicarbonsaeure-diethylester 
• 75-44-5 phosgene 

Downstream Products

• 856859-13-7 1-(4-hydroxy-3,5-dimethoxy-phenyl)-2,6-dimethyl-4-oxo-1,4-dihydro-pyridine-3,5-dicarboxylic acid diethyl ester 
• 33524-72-0 2,6-dimethyl-4-oxo-1-phenyl-1,4-dihydro-pyridine-3,5-dicarboxylic acid 
• 39905-16-3 2,6-dimethyl-4-oxo-1-phenyl-1,4-dihydro-pyridine-3,5-dicarboxylic acid diethyl ester 
• 39905-65-2 2,6,2',6'-tetramethyl-4,4'-dioxo-1,4,1',4'-tetrahydro-1,1'-p-phenylene-bis-pyridine-3,5-dicarboxylic acid tetraethyl ester 
• 1004-36-0 2,6-dimethylpyrone 
• 125732-40-3 4-ethoxycarbonyl-3-methyl-3-pyrazolin-5-one 
• 146037-86-7 3-methyl-5-oxo-2,5-dihydro-isoxazole-4-carboxylic acid ethyl ester 
• 79512-28-0 2-Hydroxy-6-methyl-4-(1,2,3,4-tetrahydroisochinolino)-isophthalsaeurediethylester 
• 64-17-5 ethanol 
• 463-79-6 carbonic-acid 

Relevant academic research and scientific papers

CHARGE CONTROL AGENT AND RELATED TECHNIQUE

[PROBLEMS] Providing a charge control agent that has a negative charge providing property at a practical level, is colorless to light-colored and usable in color toners, produces static charges stable to environmental changes by electrifying the resin pow

Diastereoselective synthesis of cis-2,6-disubstituted perhydro-4-pyranones using elevated pressure hydrogenation

A diastereoselective strategy for the synthesis of γ-pyrons was developed, starting from the Mg diacetonedicarboxylate complex. Initial cyclization with suitable anhydrides or acid chlorides, followed by hydrolytic decarboxylation leads to 2,6-disubstitut

Synthesis and Enantioselective Baeyer-Villiger Oxidation of Prochiral Perhydro-pyranones with Recombinant E. coli Producing Cyclohexanone Monooxygenase

Recombinant whole cells of Escherichia coli overexpressing Adnetobacter sp. NCIMB 9871 cyclohexanone monooxygenase (E.C. 1.14.13.22) have been utilized for the Baeyer-Villiger oxidation of prochiral perhydro-pyranones. The spatial limitations of the enzym

Condensation of Diethyl Acetonedicarboxylate. III. Isolation and Acylation of Diethyl Acetonedicarboxylate-Magnesium Complex

Diethyl acetonedicarboxylate (DADC)-magnesium complex, (DADC)2Mg (5b), was isolated from the reaction of DADC and MgCl2 with Et3N, or by the removal of coordination water from (DADC)2Mg*2H2O (5a).Compound 5b could be regarded as an intermediate in the sel