242349
2-Chloroethyl methyl ether
98%
Synonym(s):
2-Methoxyethyl chloride
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About This Item
Linear Formula:
ClCH2CH2OCH3
CAS Number:
Molecular Weight:
94.54
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
210-999-7
Beilstein/REAXYS Number:
1731028
MDL number:
Assay:
98%
Form:
liquid
InChI key
XTIGGAHUZJWQMD-UHFFFAOYSA-N
InChI
1S/C3H7ClO/c1-5-3-2-4/h2-3H2,1H3
SMILES string
COCCCl
assay
98%
form
liquid
Quality Level
bp
89-90 °C (lit.)
density
1.035 g/mL at 25 °C (lit.)
functional group
chloro, ether
Related Categories
Application
2-Chloroethyl methyl ether (2-Methoxyethyl chloride) was used in the synthesis of acyclic nucleosides of thieno[2,3-d]pyrimidine derivatives.
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Flam. Liq. 2 - Skin Irrit. 2
Storage Class
3 - Flammable liquids
wgk
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
Regulatory Information
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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
Vladimir G Krasovskiy et al.
Molecules (Basel, Switzerland), 25(12) (2020-07-02)
A number of dicationic ionic liquids with a disiloxane linker between imidazolium cations and bis(trifluoromethylsulfonyl)imide anion were synthesized and characterized. Melting points, viscosity, and volatility in a vacuum were measured; the thermal and hydrolytic stability of ionic liquids were also
P T K Lee et al.
Dalton transactions (Cambridge, England : 2003), 46(27), 8818-8826 (2017-04-01)
B(C
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