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24566-90-3

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24566-90-3 Usage

Uses

Chloromethyl octyl ether has been employed as chloromethylation reagent:in chloromethylation of calix[4]arene, methyl ethers of calix[6]arene and calix[8]arenein the synthesis of chloromethylated poly(phthalazinone ether sulfone ketone)in chloromethylation of polyetherethersulphone-polyethersulphone copolymersfor polymers

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

24566-90-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(chloromethoxy)octane

1.2 Other means of identification

Product number -
Other names chloromethyl-n-octylether

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:24566-90-3 SDS

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.

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