Ethyl diethoxyacetate, 97+%

Name: Ethyl diethoxyacetate, 97+%
SKU: L00390.14

CAS: 6065-82-3 | C8H16O4 | 176.212 g/mol

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Catalog number L00390.14

also known as L00390-14

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25 g

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Chemical Identifiers

CAS6065-82-3

IUPAC Nameethyl 2,2-diethoxyacetate

Molecular FormulaC8H16O4

InChI KeyXCLBIKIQSCTANZ-UHFFFAOYSA-N

SMILESCCOC(OCC)C(=O)OCC

Specifications

Specification Sheet

Refractive Index1.4080-1.4130 @ 20?C

FormLiquid

Appearance (Color)Clear colorless

Assay (GC)≥97.0%

Ethyl diethoxyacetate is used in the preparation of a fatty acid analog containing DTS, 12,13-dioxotetradecanoic acid di(N-methyl-thiosemicarbazone) (FA-DTS). It is used for synthesis of heterocyclic compounds.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Ethyl diethoxyacetate is used in the preparation of a fatty acid analog containing DTS, 12,13-dioxotetradecanoic acid di(N-methyl-thiosemicarbazone) (FA-DTS). It is used for synthesis of heterocyclic compounds.

Solubility
Soluble in Dichloromethane, Ethyl Acetate and Methanol.

Notes
Store in cool, dry conditions in well sealed containers. Keep container tightly closed.

RUO – Research Use Only

General References:

Charles Heidelberger.; Robert B. Hurlbert. The Synthesis of Oxalacetic Acid-1-C14 and Orotic Acid-6-C14 1. J. Am. Chem. Soc. 1950, 72, (10), 4704-4706.
Fieser, L.F.; Dunn, J.T. Synthesis of Plumbagin. J. Am. Chem. Soc. 1936, 58, (4), 572-575.
Ethyl glyoxylate equivalent. Lithiation, e.g. with lithium diethylamide, provides a useful 2-carbon fragment: Tetrahedron Lett., 4551 (1975). Reaction with the bis-Grignard from 1,4-dibromobutane gives 1-(diethoxymethyl)cyclopentanol: Canad. J. Chem., 66, 168 (1988). See also Methyl dimethoxyacetate, A12171.