66553-02-4

Basic information

• Product Name: Benzoic acid, 4,4'-(1,2-dioxo-1,2-ethanediyl)bis-, dimethyl ester
• CAS NO: 66553-02-4
• Molecular Formula: C18H14O6
• Molecular Weight: 326.306
• Mol File: 66553-02-4.mol
• Article Data: 14

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 4,4'-(1,2-dioxo-1,2-ethanediyl)bis-, dimethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 4,4'-(1,2-dioxo-1,2-ethanediyl)bis-, dimethyl ester(66553-02-4)
• EPA Substance Registry System: Benzoic acid, 4,4'-(1,2-dioxo-1,2-ethanediyl)bis-, dimethyl ester(66553-02-4)

Safety Data

• Hazardous Substances Data: 66553-02-4(Hazardous Substances Data)

Upstream product

• 104-55-2 3-phenyl-propenal 
• 1571-08-0 methyl 4-formylbenzoate 
• 16882-08-9 bis(4-(methoxycarbonyl)phenyl)acetylene 
• 198978-34-6 4-Cyanocarbonyl-benzoic acid methyl ester 
• 872-36-6 vinylene carbonate 
• 619-42-1 4-methoxycarbonylphenyl bromide 
• 40742-02-7 dimethyl 4,4′-(1-hydroxy-2-oxoethane-1,2-diyl)dibenzoate 

Downstream Products

• 1585-67-7 4,4′-oxalyldibenzoic acid 

Relevant articles and documents

Electrochemical reduction of lindane using a cobaloxime containing electron-withdrawing groups

The cobaloxime [CoCl(dbegH)2(py)] where dbegH is 4,4′?((1E,2E)?1,2?bis(hydroxyimino)ethane?1,2?diyl)dibenzoate and py is pyridine was synthesized. The electrochemical behavior was studied using cyclic voltammetry. A reversible Co(II)/Co(I) wave

A rare (3,12)-connected zirconium metal-organic framework with efficient iodine adsorption capacity and pH sensing

We report here a stable rare zirconium metal-organic framework (MOF) exhibiting a sky topology, Zr6(μ3-O)4(μ3-OH)4(ITTC)4 (UPC-158) (where H3ITTC = 4,4′,4′′-(1H-imidazole-2,4,5-t

Introduction of carbonyl groups: An approach to enhance electrochemical performance of conjugated dicarboxylate for Li-ion batteries

A rational functionalization of conjugated dicarboxylate is reported here to enhance the cyclability and rate capability for Li-ion batteries. Introduction of carbonyl groups between aromatic rings is explored as an alternative way to extend π-conjugation. For the proof of concept, 4,4′-bis(lithiooxycarbonyl)benzil (Li2-BZL) was synthesized and compared its lithium storage performance against lithium [1,1′-biphenyl]-4,4′-dicarboxylate (Li2-BPDC). The Li2-BZL electrode delivers a stable capacity of 165 mAh g?1 even after 50 cycles at current density of 50 mAh g?1 whereas, rapid capacity fading was observed in the case of Li2-BPDC. Density functional theory (DFT) studies confirmed that the carbonyl groups in the Li2-BZL to reduce the bandgap, thereby improving the elctrochemical lithium storage performance of Li2-BZL electrode in comparision to that of Li2-BPDC.