6309-62-2

Basic information

• Product Name: ethyl 2-(2-ethoxy-2-oxoethoxy)propionate
• Synonyms: ethyl 2-(2-ethoxy-2-oxoethoxy)propionate;2-(2-Ethoxy-2-oxoethoxy)propanoic acid ethyl ester;Einecs 228-629-8;ETHYL 2-(2-ETHOXY-2-OXOETHOXY)PROPANOATE(WXC08424);ETHYL 2-(2-ETHOXY-2-OXOETHOXY)PROPANOATE
• CAS NO: 6309-62-2
• Molecular Formula: C₉H₁₆O₅
• Molecular Weight: 204.22034
• EINECS: 228-629-8
• Mol File: 6309-62-2.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 260.866 °C at 760 mmHg
• Flash Point: 108.437 °C
• Appearance: /
• Density: 1.07 g/cm³
• Vapor Pressure: 0.0119mmHg at 25°C
• Refractive Index: 1.427
• CAS DataBase Reference: ethyl 2-(2-ethoxy-2-oxoethoxy)propionate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 2-(2-ethoxy-2-oxoethoxy)propionate(6309-62-2)
• EPA Substance Registry System: ethyl 2-(2-ethoxy-2-oxoethoxy)propionate(6309-62-2)

Safety Data

• Hazardous Substances Data: 6309-62-2(Hazardous Substances Data)

Usage

General Description

Ethyl 2-(2-ethoxy-2-oxoethoxy)propionate is a chemical compound typically classified as an ester. It contains an ethyl group attached to a 2-(2-ethoxy-2-oxoethoxy) propionate group. The nature of these functional groups suggests potential use in a range of industrial applications, possibly as a substrate for further chemical transformations, for solvents or as an intermediate in organic synthesis. However, information about its exact usage, potential toxicity, and behavior in the environment is sparse, highlighting the necessity for further research on this compound.

InChI:InChI=1/C9H16O5/c1-4-12-8(10)6-14-7(3)9(11)13-5-2/h7H,4-6H2,1-3H3

Upstream product

• 535-11-5 Ethyl 2-bromopropionate 
• 97-64-3 ethyl 2-hydroxypropionate 
• 105-36-2 ethyl bromoacetate 
• 38233-96-4 ethyl 2-hydroxyacetate sodium salt 
• 105-39-5 chloroacetic acid ethyl ester 

Relevant articles and documents

Synthesis and Am/Eu extraction of novel TODGA derivatives

Various ligands with structural modifications of the N,N,N',N'-tetraoctyl- 3-oxapentanediamide (TODGA) skeleton were synthesised in good yields. These modifications include (1) the increase in chain length from one carbon to two carbons between the central ether oxygen atom and the amide moieties, (2) the addition of substituents on the carbon between the central oxygen atom and the amide moieties on one and both sides of the central oxygen, (3) the replacement of the central oxygen by a (substituted) nitrogen atom and (4) synthesis of a rigidified glycolamide. The effect of the structural modifications on their extraction behaviours toward Am(III) and Eu(III) at various nitric acid concentrations was studied. In most of the cases, the extraction does not exceed that of TODGA in the entire acidity range of 0.001-4mol/l HNO3. The extraction behaviour of monomethyl-TODGA derivative 10a resembles that of TODGA at high nitric acid concentrations. However, at lower acidities, its D values are much lower, which is beneficial for possible back-extraction steps. The aza-tripodal ligands 18a,b show reverse extraction properties compared to TODGA as far as the pH influence is concerned: at pH 2, the DAm values are 49.9 and 3.1, the DEu values are 5.9 and 0.2, and the S Am/Eu values are 8 and 11, respectively.