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242349

Sigma-Aldrich

2-Chloroethyl methyl ether

98%

Synonym(s):

2-Methoxyethyl chloride

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About This Item

Linear Formula:
ClCH2CH2OCH3
CAS Number:
627-42-9
Molecular Weight:
94.54
Beilstein/REAXYS Number:
1731028
EC Number:
210-999-7
MDL number:
MFCD00000972
UNSPSC Code:
12352100
PubChem Substance ID:
24854552
NACRES:
NA.22

assay

98%

form

liquid

refractive index

n20/D 1.408 (lit.)

bp

89-90 °C (lit.)

density

1.035 g/mL at 25 °C (lit.)

SMILES string

COCCCl

InChI

1S/C3H7ClO/c1-5-3-2-4/h2-3H2,1H3

InChI key

XTIGGAHUZJWQMD-UHFFFAOYSA-N

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Application

2-Chloroethyl methyl ether (2-Methoxyethyl chloride) was used in the synthesis of acyclic nucleosides of thieno[2,3-d]pyrimidine derivatives.

pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Flam. Liq. 2 - Skin Irrit. 2

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

46.4 °F - closed cup

flash_point_c

8 °C - closed cup

ppe

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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Nasser A Hassan et al.
Nucleosides, nucleotides & nucleic acids, 26(4), 379-390 (2007-05-05)
The reaction of compounds 1, 2, 3, 4, or 13 with 2-chloroethyl methyl ether or 2,3,4,6-tetra-O-acetyl-alpha-D-glucopyranosyl bromide, afforded some acyclic and cyclic nucleosides of thieno[2,3-d]pyrimidine derivatives. Furthermore, cyclic C-nucleosides 24 and 25 were prepared from the reaction of 20, 21
P T K Lee et al.
Dalton transactions (Cambridge, England : 2003), 46(27), 8818-8826 (2017-04-01)
B(C

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