2549-47-5

Usage

Uses

Used in Plastics and Resin Production:
DIMETHYL 2,7-NAPHTHALENEDICARBOXYLATE is used as a key component in the production of plastics and resins, contributing to their structural integrity and performance characteristics. Its chemical properties allow for the creation of durable and versatile materials that can be tailored for specific applications.
Used in Chemical Manufacturing:
As a raw material, DIMETHYL 2,7-NAPHTHALENEDICARBOXYLATE is utilized in the manufacturing of various other chemicals, expanding its role in the chemical industry. Its versatility in chemical reactions enables the synthesis of a wide range of products, from pharmaceuticals to specialty chemicals.
Used in the Food Industry:
DIMETHYL 2,7-NAPHTHALENEDICARBOXYLATE is used as a flavoring agent in the food industry, enhancing the taste and aroma of various food products. Its ability to impart unique flavors and scents makes it a valuable addition to the flavorist's toolbox.
Used in the Cosmetic Industry:
In the cosmetic industry, DIMETHYL 2,7-NAPHTHALENEDICARBOXYLATE is employed as a fragrance ingredient, adding pleasant scents to personal care products. Its low toxicity and compatibility with other ingredients make it a safe and effective option for use in cosmetics.
Overall, DIMETHYL 2,7-NAPHTHALENEDICARBOXYLATE's diverse applications across different industries highlight its importance as a versatile chemical compound, with potential for further development and utilization in various sectors.

InChI:InChI=1/C14H12O4/c1-17-13(15)10-5-3-9-4-6-11(14(16)18-2)8-12(9)7-10/h3-8H,1-2H3

Upstream product

• 67-56-1 methanol 
• 17989-82-1 2,7-naphthalene dicarboxylic acid chloride 
• 201230-82-2 carbon monoxide 
• 95957-65-6 naphthalene-2,7-diyl bis(4-methylbenzenesulfonate) 
• 582-17-2 2,7-Dihydroxynaphthalene 
• 151391-00-3 methanesulfonic acid 1,1,1-trifluoro-1,1'-(2,7-naphthalenedidyl) ester 

Downstream Products

• 219316-53-7 7-Formyl-naphthalene-2-carboxylic acid benzyl ester 
• 219316-52-6 7-Hydroxymethyl-naphthalene-2-carboxylic acid benzyl ester 
• 219316-51-5 7-(tert-Butyl-dimethyl-silanyloxymethyl)-naphthalene-2-carboxylic acid benzyl ester 
• 219316-54-8 7-[(Di-tert-butoxy-phosphoryl)-hydroxy-methyl]-naphthalene-2-carboxylic acid benzyl ester 
• 219316-55-9 7-(Di-tert-butoxy-phosphoranecarbonyl)-naphthalene-2-carboxylic acid benzyl ester 
• 219316-56-0 7-[(Di-tert-butoxy-phosphoryl)-difluoro-methyl]-naphthalene-2-carboxylic acid benzyl ester 
• 162514-08-1 2-hydroxymethyl-7-methoxycarbonylnaphthalene 
• 2089-89-6 naphthalene-2,7-dicarboxylic acid 

Relevant academic research and scientific papers

Aryldifluoromethylphosphonic acids with sulfur-containing substituents as PTP-1B inhibitors

The invention encompasses the novel class of compounds represented by the formula below, which are inhibitors of the PTP-1B enzyme. The invention also encompasses pharmaceutical compositions and methods of treating or preventing PTP-1B mediated diseases,

Structure-based design and synthesis of small molecule protein-tyrosine phosphatase 1B inhibitors

Protein-tyrosine phosphatase (PTP) inhibitors are attractive as potential signal transduction-directed therapeutics which may be useful in the treatment of a variety of diseases. We have previously reported the X-ray structure of 1,1-difluoro-1-(2-naphtha

Catalyst for carbonylating naphthalene mono- and disulfonates and process using said catalyst

A cobalt based catalyst, and the method for preparing it, are disclosed. The catalyst is obtained from the reaction between NaCo(CO)4 and s-trichloro triazine and is advantageously used in the processes of carbonylation of naphthalene mono- and disulfonates in order to yield naphthalene esters and acids.

Catalyst for carbonylating naphthalene mono- and disulfonates and process using said catalyst

A cobalt based catalyst, and the method for preparing it, are disclosed. The catalyst is obtained from the reaction between NaCo(CO)4 and s-trichloro triazine and is advantageously used in the processes of carbonylation of naphthalene mono- and disulfonates in order to yield naphthalene esters and acids.

Cobalt-catalyzed methoxycarbonylation of naphthalene mono- and di-sulfonates to naphthalene mono- and di-esters

The methoxycarbonylation of naphthalene mono- and di-sulfonates under mild reaction conditions catalyzed by cobalt complexes generated in situ from either -/Me2SO4 or -/BrCH2COOEt is reported.