Diethyl 1,1-cyclobutanedicarboxylate
Diethyl 1,1-cyclobutanedicarboxylate
  • CAS No.:3779-29-1
Other grades of this product :
Diethyl 1,1-cyclobutanedicarboxylate Basic information
Product Name:Diethyl 1,1-cyclobutanedicarboxylate
Synonyms:DIETHYL CYCLOBUTANE-1,1-DICARBOXYLATE;DIETHYL 1,1-CYCLOBUTANEDICARBOXYLATE;1,1-Cyclobutanedicarboxylic Acid 1,1-Diethyl Ester;NSC 9017;1,1-Bis(ethoxycarbonyl)cyclobutane;1,1-Dicarboxylic acid cyclobutane diethylester;1,1-CYCLOBUTANEDICARBOXYLIC ACID DIETHYL ESTER;1,1-DICARBOETHOXYCYCLOBUTANE
CAS:3779-29-1
MF:C10H16O4
MW:200.23
EINECS:223-239-4
Product Categories:Building Blocks;C10 to C11;Carbonyl Compounds;Chemical Synthesis;Esters;Organic Building Blocks;Pharmaceutical Intermediates;Cyclobutanes & Cyclobutenes;Simple 4-Membered Ring Compounds;Cycloalkanes;Intermediates & Fine Chemicals;Pharmaceuticals
Mol File:3779-29-1.mol
Diethyl 1,1-cyclobutanedicarboxylate Chemical Properties
Boiling point 104-105 °C12 mm Hg(lit.)
density 1.05 g/mL at 20 °C(lit.)
refractive index 1.4360
Fp 89°C
storage temp. Sealed in dry,Room Temperature
solubility Chloroform, Dichloromethane, Methanol,
form Oil
color Colourless
Specific Gravity1.05
Water Solubility Insoluble in water.
BRN 2050195
CAS DataBase Reference3779-29-1(CAS DataBase Reference)
NIST Chemistry ReferenceDiethyl 1,1-cyclobutanedicarboxylate(3779-29-1)
EPA Substance Registry System1,1-Cyclobutanedicarboxylic acid, diethyl ester (3779-29-1)
Safety Information
Risk Statements 36/37/38
Safety Statements 23-24/25
WGK Germany 3
TSCA Yes
HS Code 38220090
MSDS Information
ProviderLanguage
SigmaAldrich English
ALFA English
Diethyl 1,1-cyclobutanedicarboxylate Usage And Synthesis
Chemical PropertiesColourless Oil
UsesDiethyl 1,1-cyclobutanedicarboxylate is used as a pharmaceutical intermediate. Used as intermediate in the production of Carboplatin.
UsesDiethyl cyclobutane-1,1-dicarboxylate may be used in chemical synthesis studies.
UsesIntermediate in the production of Carboplatin
PreparationThe preparation of diethyl 1,1-cyclobutanedicarboxylate is as follows:The major product is tetraethy1 1,1,5,5-pentanetetra-carboxylate II with diethyl malonate. To eliminate this side reaction, II was independently prepared by the addition of hydrogen bromide to diethyl allylmalonate (I) and then cyclized to II by treatment with sodium ethylate. The over-all yield from I is about 50%.

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