66644-04-0

Basic information

• Product Name: Acetic acid, 2,2'-[1,3-phenylenebis(oxy)]bis-, diethyl ester
• CAS NO: 66644-04-0
• Molecular Formula: C14H18O6
• Molecular Weight: 282.293
• Mol File: 66644-04-0.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: Acetic acid, 2,2'-[1,3-phenylenebis(oxy)]bis-, diethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Acetic acid, 2,2'-[1,3-phenylenebis(oxy)]bis-, diethyl ester(66644-04-0)
• EPA Substance Registry System: Acetic acid, 2,2'-[1,3-phenylenebis(oxy)]bis-, diethyl ester(66644-04-0)

Safety Data

• Hazardous Substances Data: 66644-04-0(Hazardous Substances Data)

Upstream product

• 6025-45-2 disodium resorcinolate 
• 105-36-2 ethyl bromoacetate 
• 105-39-5 chloroacetic acid ethyl ester 
• 108-46-3 recorcinol 
• 64-17-5 ethanol 
• 102-39-6 1,3-phenylenedioxydiacetic acid 

Downstream Products

• 102-39-6 1,3-phenylenedioxydiacetic acid 
• 791137-35-4 C₈₄H₈₈O₂₄ 
• 67045-26-5 m-phenylenedioxy-diacetyl chloride 
• 1343495-35-1 1,3-bis{(6-(4-methoxyphenyl)-1,2,4-triazolo[3,4-b][1,3,4]thiadiazol-3-yl)-methoxy}benzene 
• 1343495-34-0 1,3-bis{(6-(3,5-dinitrophenyl)-1,2,4-triazolo[3,4-b][1,3,4]thiadiazol-3-yl)-methoxy}benzene 
• 1343495-33-9 1,3-bis{(6-(4-nitriphenyl)-1,2,4-triazolo[3,4-b][1,3,4]thiadiazol-3-yl)-methoxy}benzene 
• 1343495-32-8 1,3-bis{(6-(4-bromophenyl)-1,2,4-triazolo[3,4-b][1,3,4]thiadiazol-3-yl)-methoxy}benzene 
• 1343495-31-7 1,3-bis{(6-(3-chlorophenyl)-1,2,4-triazolo[3,4-b][1,3,4]thiadiazol-3-yl)-methoxy}benzene 
• 908090-09-5 1,3-bis{(6-(4-chlorophenyl)-1,2,4-triazolo[3,4-b][1,3,4]thiadiazol-3-yl)-methoxy}benzene 
• 1343495-30-6 1,3-bis{(6-(4-fluorophenyl)-1,2,4-triazolo[3,4-b][1,3,4]thiadiazol-3-yl)-methoxy}benzene 
• 1343495-29-3 1,3-bis{(6-(3-methylphenyl)-1,2,4-triazolo[3,4-b][1,3,4]thiadiazol-3-yl)-methoxy}benzene 
• 1343495-28-2 1,3-bis{(6-(4-methylphenyl)-1,2,4-triazolo[3,4-b][1,3,4]-thiadiazol-3-yl)-methoxy}benzene 
• 1343495-27-1 1,3-bis{(6-phenyl-1,2,4-triazolo[3,4-b][1,3,4]thiadiazol-3-yl)-methoxy}benzene 
• 56970-61-7 m-phenylenedioxy-di-acetic acid dianilide 

Relevant articles and documents

Triazole-amide isosteric pyridine-based supramolecular gelators in metal ion and biothiol sensing with excellent performance in adsorption of heavy metal ions and picric acid from water

Pyridine-based small molecular gelators 1-4, having a triazole-amide isosteric relationship, have been synthesized. Compounds 1-3 exhibit excellent gelation from DMSO-H2O (1?:?2, v/v), while compound 4 forms a gel in the presence of Ag+ ions in DMSO-H2O (1?:?2, v/v). The change from triazole to isosteric amide has a marked effect on the gelling abilities, minimum gelation concentrations (mgc), thermal stability, mechanical properties, metal ion-responsive character and adsorption properties of the structures, as established by various techniques. All the gels have been successfully applied in sophisticated sensing kits for the selective detection of Cu2+ and Ag+ ions and thiol-containing amino acids. The triazole-based gelators 1 and 3 adsorb heavy metal ions from water with greater efficiency than the isosteric amide-based gelators. The metallogel 4-Ag+ can be used in the efficient removal of picric acid (a nitro explosive) from water.

Synthesis and charge-transfer complexation studies on bis(aminomethyl) m-terphenyl based bis-oxycyclophanes with intra-annular amide functionality

Bis(aminomethyl) m-terphenyl based bis-oxy cyclophanes with amide group as intra-annular functionality were synthesized and characterized from spectral and analytical data. All the cyclophanes form 1:1 charge-transfer (CT) complex with TCNQ. ARKAT-USA, Inc.

Novel synthesis of resorcinarene O-acetates by BF3·OEt2-catalyzed cyclocondensation of 1,3-(dialkoxycarbonylmethoxy)benzenes with aldehydes

Resorcinarene O-acetates, which are key intermediates in the chemical modification process of resorcinarene, can be efficiently prepared in high yields by BF3·OEt2 catalyzed cyclocondensation of 1,3-(dialkoxycarbonylmethoxy)benzenes