57847-59-3

Basic information

• Product Name: Benzoic acid, 4-chloro-, 1,2-ethanediyl ester
• CAS NO: 57847-59-3
• Molecular Formula: C16H12Cl2O4
• Molecular Weight: 339.175
• Mol File: 57847-59-3.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 4-chloro-, 1,2-ethanediyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 4-chloro-, 1,2-ethanediyl ester(57847-59-3)
• EPA Substance Registry System: Benzoic acid, 4-chloro-, 1,2-ethanediyl ester(57847-59-3)

Safety Data

• Hazardous Substances Data: 57847-59-3(Hazardous Substances Data)

Upstream product

• 107-21-1 ethylene glycol 
• 74-11-3 para-chlorobenzoic acid 
• 112-60-7 Tetraethylene glycol 
• 83691-75-2 1,6-Bis-(4-chloro-phenyl)-2,5,7,8-tetraoxa-bicyclo[4.2.0]octane 
• 73260-59-0 5,6-Bis-(4-chloro-phenyl)-2,3-dihydro-[1,4]dioxine 
• 122-01-0 4-chloro-benzoyl chloride 
• 2403-54-5 2-(4-chlorophenyl)-1,3-dioxolane 

Relevant articles and documents

Synthesis of glycol diesters through the depolymerization of polyethylene glycols with carboxylic acids using a proton-exchanged montmorillonite catalyst

A convenient and sustainable method for the synthesis of glycol diesters was developed through the depolymerization of polyethylene glycols (PEGs) with carboxylic acids using proton-exchanged montmorillonite as an efficient solid acid catalyst. Several functionalized glycol diesters were obtained in good yields from PEGs and readily available carboxylic acids. Upon reaction completion, the catalyst could be easily separated by filtration and reused with its activity remaining unchanged.

SUBSTITUENT EFFECTS ON THE DECOMPOSITION OF 1,2-DIOXETANES: A HAMMETT CORRELATION FOR SUBSTITUTED 1,6-DIARYL-1,5,7,8-TETRAOXABICYCLOY4.2.0(OCTANES

Rates of decomposition for 1,2-dioxetanes obtained from addition of singlet oxygen to substituted 2,3-diaryl-1,4-dioxenes have been found to obey a Hammett relationship with ?=++-0.24 (n 15, r 0.92).The results are taken as support for a biradical mechanism.