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14625

Bis[2-(2-chloroethoxy)ethyl] ether

≥99.0% (T)

Synonym(s):

1,11-Dichloro-3,6,9-trioxaundecane, Tetraethylene glycol dichloride

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Pack SizeSKUAvailabilityPrice
10 mL
Please contact Customer Service for Availability
PLN 437.00
50 mL
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PLN 1,520.00

About This Item

Linear Formula:
O(CH2CH2OCH2CH2Cl)2
CAS Number:
Molecular Weight:
231.12
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
1071710
Assay:
≥99.0% (T)

PLN 437.00


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Quality Level

assay

≥99.0% (T)

refractive index

n20/D 1.464

density

1.18 g/mL at 20 °C (lit.)

functional group

chloro, ether

SMILES string

ClCCOCCOCCOCCCl

InChI

1S/C8H16Cl2O3/c9-1-3-11-5-7-13-8-6-12-4-2-10/h1-8H2

InChI key

ZCFRYTWBXNQVOW-UHFFFAOYSA-N

Application

Bis[2-(2-chloroethoxy)ethyl] ether was used in preparation of series of para-(1,1,3,3-tetramethylbutyl)-phenoxypoly(ethoxy)ethanols. It was used in the synthesis of 1-(4-pyridiniumaldoxime)-2-(((2-chloroethoxy)-2-ethoxy)ethoxy)ethane[1].

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1 of 1

This Item
34170386692139548
assay

≥99.0% (T)

assay

97%

assay

≥98.0% (GC)

assay

99%

Quality Level

100

Quality Level

200

Quality Level

-

Quality Level

100

density

1.18 g/mL at 20 °C (lit.)

density

1.242 g/mL at 25 °C (lit.)

density

0.977 g/mL at 20 °C

density

0.968 g/mL at 25 °C (lit.)

refractive index

n20/D 1.464

refractive index

n20/D 1.53 (lit.)

refractive index

n20/D 1.448

refractive index

n20/D 1.446 (lit.)

functional group

chloro, ether

functional group

ether, tosylate

functional group

-

functional group

-


pictograms

Skull and crossbones

signalword

Danger

hcodes

Hazard Classifications

Acute Tox. 3 Oral - Acute Tox. 4 Dermal

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter



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Articles

Effective in key synthesis reactions like Knoevenagel condensation, thalidomide synthesis, and Suzuki coupling for sustainable chemical transformations.


Anna Hawrył et al.
Molecules (Basel, Switzerland), 25(18) (2020-09-24)
The aim of this study was to evaluate the ability of multivariate techniques to predict antioxidant and cytotoxic activity of the selected lichens from the chromatographic data. A simple and reproducible HPLC-DAD technique has been used to obtain the chromatographic
The preparation of a series of molecularly homogeneous para-t-octylphenoxypoly (ethoxy) ethanols.
Mansfield RC and Locke JE.
Journal of the American Oil Chemists' Society, 41(4), 267-272 (1964)
M C de Koning et al.
Bioorganic & medicinal chemistry, 19(1), 588-594 (2010-11-30)
A conceptually novel approach to the design of reactivators of nerve agent-inhibited acetylcholinesterase (AChE) is presented. The concept comprises the linkage of a peripheral site ligand via a spacer to a reactivating moiety with the eventual goal to develop non-ionic



Global Trade Item Number

SKUGTIN
454850-25G04061832541105
454850-5G04061832541112
14625-10ML04061837014031
14625-50ML04061837014048

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