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ChemicalBook >  Product Catalog >  Chemical Reagents >  Organic reagents >  Esters >  1,1,2,3-PROPANETETRACARBOXYLIC ACID TETRAETHYL ESTER

1,1,2,3-PROPANETETRACARBOXYLIC ACID TETRAETHYL ESTER

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1,1,2,3-PROPANETETRACARBOXYLIC ACID TETRAETHYL ESTER Basic information

Product Name:
1,1,2,3-PROPANETETRACARBOXYLIC ACID TETRAETHYL ESTER
Synonyms:
  • propanetetracarboxylicacidtetraethylester
  • 1,1,2,3-PROPANETETRACARBOXYLIC ACID TETRAETHYL ESTER
  • TETRAETHYL PROPANE-1,1,2,3-TETRACARBOXYLATE
  • 2,3-Bis(ethoxycarbonyl)pentanedioic acid diethyl ester
  • Propane-1,1,2,3-tetracarboxylic Acid Tetraethyl Ester
  • TetraethylPropane-1,1,2,3-tetracarboxylate>
  • 1,1,2,3-Propanetetracarboxylic acid, 1,1,2,3-tetraethyl ester
CAS:
635-03-0
MF:
C15H24O8
MW:
332.35
EINECS:
211-222-4
Mol File:
635-03-0.mol
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1,1,2,3-PROPANETETRACARBOXYLIC ACID TETRAETHYL ESTER Chemical Properties

Boiling point:
389.48°C (rough estimate)
Density 
1.1184
refractive index 
1.4380-1.4420
pka
11.42±0.59(Predicted)
form 
clear liquid
color 
Colorless to Almost colorless
InChIKey
WGEVJRBJWMGTSI-UHFFFAOYSA-N
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Safety Information

HS Code 
2917.19.7050
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1,1,2,3-PROPANETETRACARBOXYLIC ACID TETRAETHYL ESTER Usage And Synthesis

Uses

1,1,2,3-PROPANETETRACARBOXYLIC ACID TETRAETHYL ESTER can be used as organic synthesis intermediate and pharmaceutical intermediate, mainly used in laboratory research and development process and chemical production process.

Synthesis


Condensation of diethylfumarate and diethylmalonate to propane-1,1,2,3 tetracarboxylate. Catalyst specifications: Catalytic entity: Ph(CH2)-N+(PhmSO3-)3 · EtO- (1 milieq of EtO-), additive:: Sodium meta silicate 1 gm, Support: Charcoal 5 gm, Group IIA metal salt: Barium hydroxide, Method of preparation: Deposition precipitation. Procedure: in a 100-ml flask fitted with an efficient reflux condenser, magnetic stirrer bar and dropping funnel was charged 5 gm of catalyst. With stirring 1.6 g (0.001 mol) diethylmalonate and 25 ml dry ethanol was added. Reaction mixture was warmed and 1.4 gm (0.0081 mol) diethyl fumarate was added. Mixture was refluxed for 8 hours. Reaction mixture was cooled and suspension was centrifuged to recover catalyst. Analysis of reaction liquid indicated 90 % conversion for diethylmalonate. Product was distilled under vacuum 8 mm at 180-190°C to obtain propane-1,1,2,3 tetracarboxylate 85% yield. Catalyst was recovered and washed with ethanol, diethyl ether and dried under vacuum. Catalyst was recycled to obtain equivalent activity.

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