24566-90-3 Usage
Description
Chloromethyl octyl ether is an organic compound that serves as a versatile chloromethylation reagent in various chemical reactions and synthesis processes. It is characterized by its ability to introduce chloromethyl groups into different substrates, making it a valuable intermediate in the production of various polymers and other chemical compounds.
Uses
Used in Calixarene Synthesis:
Chloromethyl octyl ether is used as a chloromethylation reagent for the synthesis of chloromethylated calix[4]arene, methyl ethers of calix[6]arene, and calix[8]arene. It plays a crucial role in the formation of these complex organic structures, which have potential applications in various fields, including supramolecular chemistry and molecular recognition.
Used in Polymer Synthesis:
Chloromethyl octyl ether is employed in the synthesis of chloromethylated poly(phthalazinone ether sulfone ketone), a high-performance polymer with excellent thermal stability and mechanical properties. This polymer finds applications in aerospace, automotive, and electronics industries due to its outstanding characteristics.
Used in Polyetheretherketone (PEEK) Modification:
Chloromethyl octyl ether is used as a chloromethylation reagent for the modification of polyetherethersulphone-polyethersulphone (PES-PES) copolymers. The introduction of chloromethyl groups into the polymer structure enhances its properties, such as hydrophilicity and biocompatibility, making it suitable for various applications, including medical devices and drug delivery systems.
Used in Polymer Industry:
In the polymer industry, chloromethyl octyl ether is utilized as a chloromethylation agent for the functionalization of various polymers. This modification allows for the creation of new materials with improved properties, such as enhanced reactivity, solubility, and compatibility with other polymers, which can be tailored for specific applications in different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 24566-90-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,5,6 and 6 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 24566-90:
(7*2)+(6*4)+(5*5)+(4*6)+(3*6)+(2*9)+(1*0)=123
123 % 10 = 3
So 24566-90-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H19ClO/c1-2-3-4-5-6-7-8-11-9-10/h2-9H2,1H3
24566-90-3Relevant articles and documents
Ionic liquids with symmetrical dialkoxymethyl-substituted imidazolium cations
Pernak, Juliusz,Sobaszkiewicz, Kinga,Foksowicz-Flaczyk, Joana
, p. 3479 - 3485 (2004)
A new one-step procedure is described for the synthesis of disubstituted imidazolium chlorides. 1,3-Dialkoxymethylimidazolium chlorides thus obtained can be employed as synthetic precursors of symmetrical ILs. The salts have been found to exhibit antimicrobial activity and an antielectrostatic effect. Their densities and viscosities have been determined and are reported herein. It has also been demonstrated that the ILs can be decomposed using an aqueous solution of KMnO4. For each IL, the permanganate index (IMn) has been estimated, which varies with the structure of cation. The only limitation of IMn is the degree to which the IL dissolves in water.
Donepezil myristyloxymethyl ether or its pharmaceutically acceptable salt
-
Paragraph 0109-0111; 0121-0123, (2019/10/08)
The present invention relates to a novel donepezil myristyloxymethyl ether or a pharmaceutically acceptable salt thereof, and a sustained-release pharmaceutical composition containing the same as a main component. Donepezil myristyloxymethyl ether of the
3-Alkoxymethyl-1-(1R,2S,5R)-(-)-menthoxymethylimidazolium salts-based chiral ionic liquids
Feder-Kubis, Joanna,Kubicki, MacIej,Pernak, Juliusz
experimental part, p. 2709 - 2718 (2011/02/16)
A new group of imidazolium salt-based chiral ionic liquids have been prepared and characterized. The chiral ionic liquids obtained are stable in air, in contact with water and popular organic solvents. Their physicochemical properties, single-crystal X-ray structures, antimicrobial activities, and antielectrostatic effects have been determined. The chiral ionic liquids synthesized have proven to represent not only potential new solvents in asymmetric synthesis but also effective disinfectants with antielectrostatic activity.
