Diethyl 1,1-cyclobutanedicarboxylate

Diethyl 1,1-cyclobutanedicarboxylate Basic information
Product Name:Diethyl 1,1-cyclobutanedicarboxylate
Synonyms: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;AKOS BBS-00006459
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;Intermediates & Fine Chemicals;Pharmaceuticals;Cyclobutanes & Cyclobutenes;Simple 4-Membered Ring Compounds;Cycloalkanes
Mol File:3779-29-1.mol
Diethyl 1,1-cyclobutanedicarboxylate Structure
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 cyclobutane-1,1-dicarboxylate may be used in chemical synthesis studies.
UsesDiethyl 1,1-cyclobutanedicarboxylate is used as a pharmaceutical intermediate. Used as intermediate 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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Cyclobutanecarboxaldehyde 1-Pyrrolidinecarboxylicacid,4-amino-2-methyl-,1,1-dimethylethylester,(2S,4R)-(9CI) CYCLOBUTANECARBOXAMIDINE HYDROCHLORIDE 3-Piperidin-4-yl-azetidine-1-carboxylic acid tert-butyl ester CYCLOBUTANECARBOXAMIDE 2-PHENYL-CYCLOBUTANE-1,1-DICARBOXYLIC ACID DIETHYL ESTER Dimethylmalonic acid 2,2-DIMETHYL-MALONIC ACID MONOMETHYL ESTER Ethyl cyclobutanecarboxylate PROPYLMALONIC ACID Dimethyl propylmalonate DIETHYL 1,1-CYCLOBUTANEDICARBOXYLATE (1,1-CYCLOBUTANEDICARBOXYLIC ACID DIETHYL ESTER) HYDROXYPIVALIC ACID METHYL ESTER 7-Chloro-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxoquinoline-3-carboxylic acid Mefenpyr-diethyl DIETHYL 3-ETHYLCYCLOBUTANE-1,1-DICARBOXYLATE Cyclopropanecarboxylic acid CYCLOBUTANE-1,1-DIYLDIMETHANOL

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