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Usage

Uses

Used in Polymer Synthesis:
DIETHYL TEREPHTHALOYLDIACETATE is used as a building block in the synthesis of polymers, particularly as a monomer for the production of polyester resins and fibers. Its properties contribute to the creation of materials with enhanced durability and performance.
Used in Adhesives Production:
In the adhesives industry, DIETHYL TEREPHTHALOYLDIACETATE is used as a key component in the formulation of high-quality adhesives. Its chemical resistance and thermal stability ensure the production of adhesives that can withstand harsh conditions and maintain their bonding strength.
Used in Coatings Industry:
DIETHYL TEREPHTHALOYLDIACETATE is utilized in the coatings industry to produce coatings with improved durability, chemical resistance, and thermal stability. These coatings are suitable for various applications, including automotive, aerospace, and industrial settings.
Used in Plastic Materials Manufacturing:
The plastic materials industry employs DIETHYL TEREPHTHALOYLDIACETATE in the production of high-performance plastics. These plastics are known for their ability to resist chemicals and maintain their structural integrity at elevated temperatures, making them ideal for a wide range of applications.
Used in Pharmaceutical Production:
DIETHYL TEREPHTHALOYLDIACETATE serves as an intermediate in the production of pharmaceuticals. Its role in the synthesis process contributes to the development of various medications that address different health conditions.
Used in Agrochemicals Production:
In the agrochemicals industry, DIETHYL TEREPHTHALOYLDIACETATE is used as an intermediate in the synthesis of various agrochemical products. Its involvement in the production process helps create effective solutions for agricultural applications.
Used in Specialty Chemicals Production:
DIETHYL TEREPHTHALOYLDIACETATE is also utilized as an intermediate in the production of specialty chemicals. Its unique properties allow for the creation of specialized chemical products that cater to specific industrial needs.

Upstream product

• 100-20-9 terephthaloyl chloride 
• 1009-61-6 1,4-Diacetylbenzene 
• 105-58-8 Diethyl carbonate 

Downstream Products

• 92-21-7 3,3'-dioxo-3,3'-p-phenylene-di-propionic acid bis-(5-chloro-2,4-dimethoxy-anilide) 
• 109730-02-1 3,3'-dioxo-3,3'-p-phenylene-di-propionic acid bis-(4-chloro-anilide) 
• 114141-87-6 1,4-bis<1-phenyl-3-(3'-pyridyl)-6(1H)-oxopyrano<2,3-c>pyrazolin-4-yl>benzene 
• 30020-89-4 3,3'-dimethyl-1,1'-diphenyl-1H,1'H-4,4'-p-phenylene-bis-pyrano[2,3-c]pyrazol-6-one 
• 6492-81-5 3,3'-dioxo-3,3'-p-phenylene-di-propionic acid bis-(4-chloro-2-methoxy-5-methyl-anilide) 
• 71334-20-8 3,3'-dioxo-3,3'-p-phenylene-di-propionic acid dianilide 
• 1009-61-6 1,4-Diacetylbenzene 

Relevant academic research and scientific papers

Synthesis of 6-arylisocytosines and their potential for hydrogen bonding interactions

Abstract The synthesis of a number of 6-arylisocytosines, including linked bis-isocytosines, from the reaction of guanidine with β-ketoesters is described. The compounds were investigated for their ability to form hydrogen-bonded structural networks, and for their potential interactions with the telomeric quadruplex forming sequence AGGG(TTAGGG)3.

Convenient synthesis and characterization of molecules containing multiple β-keto ester units

Three compounds containing two β-keto ester units and one containing three were obtained in good yields from sebacyl, terepthaloyl, isophthaloyl, and trimesoyl chlorides. In this one pot procedure the acid chlorides were first treated with ethyl acetoacetate and barium oxide and then with ethyl alcohol. The aliphatic ester exists mainly as keto ester with a very small amount of the enol tautomer. In the case of aromatic esters, all possible tautomers were found in considerable concentrations in deuterochloroform solution. Theoretical chemical shifts were estimated from GIAO/WP04/aug - cc-pVDZ/SCRF calculations, for a probable signal assignation for the corresponding tautomeric species. Our theoretical results are in agreement with experimental findings and account for negligible stability differences between the tautomers of each aromatic compound.