6309-62-2 Usage
Uses
Used in Chemical Synthesis:
Ethyl 2-(2-ethoxy-2-oxoethoxy)propionate is used as an intermediate in chemical synthesis for its potential role in creating more complex molecules. Its ester functionality may allow for further reactions, making it a valuable component in the synthesis of various organic compounds.
Used in Solvent Applications:
Due to its chemical structure, ethyl 2-(2-ethoxy-2-oxoethoxy)propionate may be employed as a solvent in certain industrial processes. Its ability to dissolve other substances could be beneficial in applications where a specific solvent with its particular properties is required.
Used in Pharmaceutical Industry:
Ethyl 2-(2-ethoxy-2-oxoethoxy)propionate is used as a potential substrate for the development of pharmaceutical compounds. Its reactivity and functional groups may contribute to the creation of new drug molecules, although further research is needed to explore its full potential in this area.
Used in Environmental Research:
Given the limited information on the toxicity and environmental impact of ethyl 2-(2-ethoxy-2-oxoethoxy)propionate, it is used as a subject of study in environmental research. Understanding its behavior in the environment is crucial for assessing its safety and potential ecological effects.
Check Digit Verification of cas no
The CAS Registry Mumber 6309-62-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,0 and 9 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6309-62:
(6*6)+(5*3)+(4*0)+(3*9)+(2*6)+(1*2)=92
92 % 10 = 2
So 6309-62-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H16O5/c1-4-12-8(10)6-14-7(3)9(11)13-5-2/h7H,4-6H2,1-3H3
6309-62-2Relevant academic research and scientific papers
Synthesis and Am/Eu extraction of novel TODGA derivatives
Iqbal, Mudassir,Huskens, Jurriaan,Verboom, Willem,Sypula, Michal,Modolo, Giuseppe
experimental part, p. 827 - 837 (2011/12/02)
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.
