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Merck
CN

238155

2-Bromoethyl methyl ether

Synonym(s):

1-Bromo-2-methoxyethane

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About This Item

Linear Formula:
BrCH2CH2OCH3
CAS Number:
Molecular Weight:
138.99
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
229-339-4
MDL number:
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InChI key

YZUPZGFPHUVJKC-UHFFFAOYSA-N

InChI

1S/C3H7BrO/c1-5-3-2-4/h2-3H2,1H3

SMILES string

COCCBr

form

liquid

refractive index

n20/D 1.447 (lit.)

bp

40-41 °C/66 mmHg (lit.)

solubility

water: soluble 14.4 g/L at 25 °C

density

1.479 g/mL at 25 °C (lit.)

functional group

bromo
ether

storage temp.

2-8°C

Quality Level

Application

2-Bromoethyl methyl ether has been used as starting reagent in the synthesis of 1-bromo-4-(2-methoxyethoxy)benzene and 1-bromo-4-[(2-methoxyethoxy)methyl]benzene.

General description

Kinetics of potassium iodide exchange reaction with 2-bromoethyl methyl ether in acetone at 15 and 25°C has been investigated.

pictograms

FlameSkull and crossbones

signalword

Danger

Hazard Classifications

Acute Tox. 3 Oral - Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

3 - Flammable liquids

wgk

WGK 3

flash_point_f

82.4 °F - closed cup

flash_point_c

28 °C - closed cup

ppe

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

Regulatory Information

危险化学品
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Alex R Neale et al.
Chemphyschem : a European journal of chemical physics and physical chemistry, 18(15), 2040-2057 (2017-05-19)
A series of hydrophobic room temperature ionic liquids (ILs) based on ethereal functionalised pyrrolidinium, piperidinium and azepanium cations bearing the bis[(trifluoromethyl)sulfonyl]imide, [TFSI]
Novel water-soluble organosilane compounds as a radical reducing agent in aqueous media.
Yamazaki O, et al.
Bulletin of the Chemical Society of Japan, 70, 2519-2523 (1997)
Forrest S Gittleson et al.
Physical chemistry chemical physics : PCCP, 21(31), 17176-17189 (2019-07-26)
Ionic liquids are a unique class of materials with several potential applications in electrochemical energy storage. When used in electrolytes, these highly coordinating solvents can influence device performance through their high viscosities and strong solvation behaviors. In this work, we
Ulderico Ulissi et al.
ChemSusChem, 11(1), 229-236 (2017-09-30)
The room-temperature molten salt mixture of N,N-diethyl-N-(2-methoxyethyl)-N-methylammonium bis(trifluoromethanesulfonyl) imide ([DEME][TFSI]) and lithium bis(trifluoromethanesulfonyl)imide (LiTFSI) salt is herein reported as electrolyte for application in Li-O
The Iodide Ion Exchange Reaction with 2-Haloethyl Alkyl Ethers and n-Butyl Bromide1.
Tutwiler FB and McKee RL.
Journal of the American Chemical Society, 76(24), 6342-6344 (1954)

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