5897-78-9

Basic information

• Product Name: Acetic acid, 2,2'-[1,4-phenylenebis(oxy)]bis-, diethyl ester
• CAS NO: 5897-78-9
• Molecular Formula: C14H18O6
• Molecular Weight: 282.293
• Mol File: 5897-78-9.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: Acetic acid, 2,2'-[1,4-phenylenebis(oxy)]bis-, diethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Acetic acid, 2,2'-[1,4-phenylenebis(oxy)]bis-, diethyl ester(5897-78-9)
• EPA Substance Registry System: Acetic acid, 2,2'-[1,4-phenylenebis(oxy)]bis-, diethyl ester(5897-78-9)

Safety Data

• Hazardous Substances Data: 5897-78-9(Hazardous Substances Data)

Upstream product

• 64-17-5 ethanol 
• 2245-53-6 2,2'-[1,4-phenylenebis(oxy)]bisacetic acid 
• 105-36-2 ethyl bromoacetate 
• 123-31-9 hydroquinone 

Downstream Products

• 157108-67-3 diethyl 2,2'-<2,5-bis(chloromethyl)phen-1,4-ylenedioxy>bis(acetate) 
• 20276-98-6 hydroquinone-1,4-diacetyl dihydrazide 
• 100876-88-8 1,4-bis[(N-2-hydroxyethyl)carbamoylmethoxy]benzene 
• 104-38-1 1,4-bis(2-hydroxyethoxy)benzene 
• 98682-96-3 1,4-Bis-<β-(acetoacetoxy)-aethoxy>-benzol 
• 1282454-21-0 C₅₈H₅₂Cl₄O₁₂ 
• 1282454-05-0 C₆₂H₆₄O₈ 
• 1282453-88-6 C₆₆H₇₂O₁₆ 
• 1282453-86-4 C₆₂H₆₄O₁₄ 
• 1282453-84-2 C₅₈H₅₆O₁₂ 
• 1282453-34-2 C₆₂H₇₂O₈ 
• 1282453-25-1 C₅₄H₅₆O₈ 
• 1282453-11-5 C₅₂H₅₂O₈ 
• 1282454-83-4 C₄₀H₃₈O₄ 

Relevant articles and documents

A one-pot synthesis of a self-included bisester-functionalized copillar[5]arene

We report here a one-pot synthetic method for the synthesis of a bisester-functionalized copillar[5]arene (BECP5A) with yield up to 20%. The properties of BECP5A in solution and in solid state were deeply investigated with the aid of 1D and 2D NMR spectra

One-pot synthesis of cyclophane-type macrocycles using manganese(iii)- mediated oxidative radical cyclization

Cyclophane-type macrocyclic compounds from 21 to 56 members having two fused dihydrofuran rings were synthesized by the manganese(iii)-mediated oxidation of terminal dienes with bis(3-oxobutanoate)s containing aromatics. The reaction detail, characterization and reaction pathways are described. The Royal Society of Chemistry 2011.

Polymeric salen-Ti(IV) or V(V) complex catalyzed asymmetric synthesis of O-acetylcyanohydrins from KCN, Ac2O and aldehydes

Polymeric salen-Ti(IV) and V(V) complexes were employed in the enantioselective O-acetyl cyanation of aldehydes with potassium cyanide and acetic anhydride. The crosslinked polymeric salen-Ti(IV) catalyst exhibited good activities and enantioselectivities, up to 91% ee with 99% conversion was obtained at -20°C with 1 mol% of catalyst (based on bimetallic catalytic unit). Moreover, six consecutive recyclings with the easily recovered crosslinked polymeric catalyst showed no obvious decrease in either activity or enantioselectivity. Linear polymeric salen-V(V) catalyst showed good catalytic efficiency too, up to 94% ee with 99% conversion was obtained at -42°C with 5 mol% of catalyst. Graphical Abstract.