Skip to Content
Merck
All Photos(1)

Documents

382205

Sigma-Aldrich

2-Bromoethyl ether

technical grade, 90%

Synonym(s):

Bis(2-bromoethyl) ether

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
(BrCH2CH2)2O
CAS Number:
Molecular Weight:
231.91
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

grade

technical grade

Assay

90%

form

liquid

bp

92-93 °C/12 mmHg (lit.)

density

1.845 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

BrCCOCCBr

InChI

1S/C4H8Br2O/c5-1-3-7-4-2-6/h1-4H2

InChI key

FOZVXADQAHVUSV-UHFFFAOYSA-N

General description

2-Bromoethyl ether (2,2′-Dibromodiethyl ether) is a halogen containing ether. 2,2′-Dibromodiethyl ether has been prepared by reacting dioxane with anhydrous, bromine free hydrogen bromide.

Application

2-Bromoethyl ether (2,2′-Dibromodiethyl ether) may be used in the preparation of 1,4,7-trioxa-10-19-dithia-13,16-diaza-12,17-dioxo-8,9,14,15,20,21-tribenzoheneicosane.
2-Bromoethyl ether may be used in the synthesis of macroheterocycles including redox-active tetrathiafulvalene linked systems and polyoxaza cryptands.

Pictograms

CorrosionExclamation mark

Signal Word

Danger

Hazard Statements

Precautionary Statements

Hazard Classifications

Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

185.0 °F

Flash Point(C)

85 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

The reaction of dioxane with hydrogen bromide.
Cleave ABV and Blake RI.
Canadian Journal of Chemistry, 29(9), 785-789 (1951)
Ping-Yu Wu et al.
The Journal of organic chemistry, 71(2), 833-835 (2006-01-18)
[reaction: see text] A mild asymmetric arylation of aromatic aldehydes catalyzed by gamma-amino thiol 5 gave the corresponding diarylmethanols with 95 to >99.5% ee.
J. Chem. Soc. Perkin Trans. II, 1213-1213 (1989)
Journal of the Chemical Society. Chemical Communications, 1550-1550 (1992)
New approach to the synthesis of dibenzodithia-and benzothiaazacrown ethers via the aromatization of 2-alkylthio (arylthio) cyclohexanes during bromination.
Kudryatsev KV and Samofin VV.
Chemistry of Heterocyclic Compounds, 33(1), 106-111 (1997)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service