10220-23-2 Usage
Uses
Used in Pharmaceutical Industry:
4-(2-methoxyethyl)morpholine is used as a solvent for the production of pharmaceuticals, facilitating the synthesis and formulation of various drugs. Its ability to dissolve a wide range of compounds makes it a valuable component in this field.
Used in Agrochemical Industry:
In the agrochemical sector, 4-(2-methoxyethyl)morpholine serves as a solvent in the manufacturing process of agrochemicals, aiding in the development of effective and safe products for agricultural use.
Used in Polymer Additives Industry:
4-(2-methoxyethyl)morpholine is utilized as a solvent for the production of polymer additives, contributing to the enhancement of polymer properties and performance in various applications.
Used as a Stabilizer and Corrosion Inhibitor in Metalworking Fluids:
MEM is employed as a stabilizer and corrosion inhibitor in metalworking fluids, improving the longevity and efficiency of these fluids in industrial processes.
Used in Organic Synthesis:
4-(2-methoxyethyl)morpholine is used as a building block and intermediate in organic synthesis, enabling the preparation of other chemical compounds for diverse applications.
Each of these applications takes advantage of the unique properties of 4-(2-methoxyethyl)morpholine, such as its solubility and stability, to contribute to the effectiveness and advancement of the respective industries.
Check Digit Verification of cas no
The CAS Registry Mumber 10220-23-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,2,2 and 0 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 10220-23:
(7*1)+(6*0)+(5*2)+(4*2)+(3*0)+(2*2)+(1*3)=32
32 % 10 = 2
So 10220-23-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H15NO2/c1-9-5-2-8-3-6-10-7-4-8/h2-7H2,1H3
10220-23-2Relevant academic research and scientific papers
Processes for the preparation of aminoethers
-
, (2008/06/13)
A process for preparing aminoethers, particularly bis[2-(N,N-dialkylamino)alkyl]ethers, which comprises contacting a carboxylated aminoether with a metal oxide catalyst under conditions effective to produce the aminoether. Many of these aminoethers are useful as catalysts in the production of polyurethanes, especially cellular polyurethanes.
Decarboxylation processes using mixed metal oxide catalysts
-
, (2008/06/13)
A decarboxylation process which comprises contacting a carboxylated compound with a metal oxide catalyst under conditions effective to decarboxylate the carboxylated compound.
Twelve-ring Azacrowns with 2-Alkoxyethyl Side Arms
Buoen, Solfrid,Dale, Johannes
, p. 278 - 282 (2007/10/02)
The hydrophilic azacrown ligand 1,4,7,10-tetrakis(2-hydroxyethyl)-1,4,7,10-tetraazacyclododecane can be easily tetramethylated and tetraethylated.Complexation with sodium salts remains strong for both derivatives in chloroform, but extraction with water removes NaI from its complex with the tetraethylated ligand.Pyrolysis of complexes of the tetramethylated ligand liberates the ligand if pure, but results in degradation to 1,4-bis(2-methoxyethyl)piperazine if traces of alkylation reagent are present.The methylated derivative is also obtained by cyclooligomerization of N-(2-methoxyethyl)aziridine, which is hovewer difficult to prepare.The direct reaction between ethyleneglycol ditosylate and 2-methoxyethaneamine (1:1) gives mainly the piperazine, but with excess of amine a series of acyclic oligoamines are obtained.Attempts to prepare 12-azacrowns by reacting the triamine with tosylated diethylamine or diethylamine glycol led instead to six-ring compounds.
