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112-26-5

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112-26-5 Usage

Chemical Properties

clear colorless to pale yellow liquid. Insoluble in water. Combustible.

Uses

Different sources of media describe the Uses of 112-26-5 differently. You can refer to the following data:
1. Solvent for hydrocarbons, oils, etc.; extractant; intermediate for resins and insecticides; organic synthesis.
2. 1,2-Bis(2-chloroethoxy)ethane is used as pharmaceutical intermediate.
3. 1,2-bis(2-chloroethoxy)ethane was used in the synthesis of 1,1′-[1,2-ethanediylbis(oxy-1,2-ethanediyl)]bis[3-methyl-1H-imidazolium-1-yl] chloride.

Check Digit Verification of cas no

The CAS Registry Mumber 112-26-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,1 and 2 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 112-26:
(5*1)+(4*1)+(3*2)+(2*2)+(1*6)=25
25 % 10 = 5
So 112-26-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H12Cl2O2/c1-6(9-4-2-7)10-5-3-8/h6H,2-5H2,1H3

112-26-5 Well-known Company Product Price

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  • (Code)Product description
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  • Detail
  • Alfa Aesar

  • (B22884)  1,2-Bis(2-chloroethoxy)ethane, 97%   

  • 112-26-5

  • 100g

  • 404.0CNY

  • Detail
  • Alfa Aesar

  • (B22884)  1,2-Bis(2-chloroethoxy)ethane, 97%   

  • 112-26-5

  • 500g

  • 1235.0CNY

  • Detail

112-26-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-Bis(2-chloroethoxy)ethane

1.2 Other means of identification

Product number -
Other names TRIGLYCOL DICHLORIDE

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Intermediates
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:112-26-5 SDS

112-26-5Relevant articles and documents

Ionic liquid-type crown ether as a novel medium for a liquid/liquid extraction of radioactive metal ion85Sr2+

Sang, Hyun Park,Dorjnamjin, Demberelnyamba,Seung, Ho Jang,Myung, Woo Byun

, p. 1024 - 1025 (2006)

1,13-Dichloro-4,7,10-trioxatridecane (2-[2-(1-chloro-2-ethoxy)ethoxy]ethyl chloride) (3a) was synthesized by a chlorination of 1,13-dihydroxy-4,7,10- trioxatridecane (triethylene glycol). And it was treated with imidazole and sodium ethoxide to give the 1N,1N′(oxoethylene)-diimidazole (3b), which was then converted to ionic liquid-type crown ether (ILCE) 3 with a reaction with 1,9-dichloro-3,6-trioxaoctane (2a). Further, the anion of ILCE was exchanged by an anion-exchange method. Ultimately, we developed a very efficient synthetic pathway for ILCEs 1-4 which have various physical and chemical characteristics by a modification of the polyethylene glycol chain length and anions. 85Sr2+ was successfully extracted into the [(3,2)OEtIm][Cl] (3) phase, but it was not extracted into the [(2,2)OEtIm][Cl] (1), [(3,3)OEtIm][Cl] (2), and [(4,3)OEtIm][Cl] (4) phases. Copyright

Design of task-specific ionic liquids for catalytic conversion of CO 2 with aziridines under mild conditions

Zhao, Ya-Nan,Yang, Zhen-Zhen,Luo, Si-Hang,He, Liang-Nian

, p. 2 - 8 (2013/02/23)

A series of polyethylene glycol (PEG)-functionalized ionic liquids (ILs) were developed as recyclable and efficient catalysts for selective synthesis of 5-aryl-2-oxazolidinones from aziridines and CO2 without addition of any organic solvents or additives. In particular, high yields, chemo- and regio-selectivities of oxazolidinones were attained when BrDBNPEG 150DBNBr (DBN: 1,5-diazabicyclo[4.3.0]non-5-ene) was used as the catalyst, presumably due to activation of CO2 by the ether linkage in the PEG backbone, and stabilization of the ring-opened species of aziridine by the delocalized cation BrDBNPEG150DBN+. Furthermore, the catalyst could be reused for over four consecutive cycles without appreciable loss of catalytic activity and selectivity. The effects of catalyst structure and various reaction parameters on the catalytic performance were also investigated in detail. It was demonstrated that the catalyst worked well for a variety of aziridines producing the corresponding oxazolidinones in good yields and excellent regio-selectivities. Therefore, this solvent-free process could thus represent an environmentally friendly approach for ILs-catalyzed conversion of CO2 into value-added chemicals.

SYNTHESIS OF DIFUNCTIONAL OXYETHYLENE-BASED COMPOUNDS

-

Page/Page column 2-3, (2009/07/25)

A method of reacting a toluenesulfonyl-terminated polyoxyethylene compound having the formula CH3—C6H4—SO2—(O—CH2—CH2)n—O—R1 with an ammonium salt having the formula NR24X to form a compound having the formula X—CH2—CH2—(O—CH2—CH2)n-1—R3. The value n is a positive integer. X is a halogen, cyanide, cyanate, thiocyanate, or azide. R1 is a terminating group. Each R2 is hydrogen or an alkyl group. —R3 is —O—R1 or —X.

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