242349
2-Chloroethyl methyl ether
98%
Synonym(s):
2-Methoxyethyl chloride
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PLN 140.00
100 G
PLN 653.00
PLN 140.00
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5 G
PLN 140.00
100 G
PLN 653.00
About This Item
Linear Formula:
ClCH2CH2OCH3
CAS Number:
Molecular Weight:
94.54
Beilstein:
1731028
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
PLN 140.00
List PricePLN 200.00Save 30%Please contact Customer Service for Availability
Request a Bulk Order
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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.)
functional group
chloro
ether
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[1].
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Flam. Liq. 2 - Skin Irrit. 2
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point(F)
46.4 °F - closed cup
Flash Point(C)
8 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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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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