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Sigma-Aldrich

1-Bromo-2-chloroethane

98%

Synonym(s):

Ethylene bromochloride, Ethylene chlorobromide

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About This Item

Linear Formula:
ClCH2CH2Br
CAS Number:
107-04-0
Molecular Weight:
143.41
Beilstein:
605265
EC Number:
203-456-0
MDL number:
MFCD00000962
UNSPSC Code:
12352100
PubChem Substance ID:
24853925
NACRES:
NA.22

Assay

98%

form

liquid

refractive index

n20/D 1.488 (lit.)

bp

106-107 °C (lit.)

mp

−18-−14 °C (lit.)

solubility

water: soluble

density

1.723 g/mL at 25 °C (lit.)

SMILES string

ClCCBr

InChI

1S/C2H4BrCl/c3-1-2-4/h1-2H2

InChI key

IBYHHJPAARCAIE-UHFFFAOYSA-N

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General description

Dissociative double ionization and multi-photon ionization of 1-bromo-2-chloroethane (BCE) irradiated by the 800nm femtosecond laser field has been investigated by dc-slice imaging technology. Conformational properties of BCE in several zeolites such as silicalite-1, siliceous Y, Na-Y and zeolite L have been investigated by FT-Raman spectroscopy.

Application

1-Bromo-2-chloroethane was used in regio- and diastereoselective synthesis of 2-alkylidenetetrahydrofurans.

Pictograms

Skull and crossbonesHealth hazard
GHS06,GHS08

Signal Word

Danger

Hazard Classifications

Acute Tox. 3 Oral - Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Carc. 1B - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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’.

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P Langer et al.
The Journal of organic chemistry, 66(18), 6057-6063 (2001-09-01)
The domino C,O-cyclodialkylation reaction of dilithiated 1,3-dicarbonyl compounds with 1,4-dibromo-2-butene resulted in regio- and diastereoselective formation of 2-alkylidene-5-vinyltetrahydrofurans. The cyclization of 1,3-dicarbonyl dianions with 1-bromo-2-chloroethane regio- and diastereoselectively afforded 2-alkylidenetetrahydrofurans under thermodynamic reaction control.
Yan Yang et al.
The Journal of chemical physics, 135(6), 064303-064303 (2011-08-17)
The dissociative double ionization and multi-photon ionization of 1-bromo-2-chloroethane (BCE) irradiated by the 800 nm femtosecond laser field have been investigated by dc-slice imaging technology. The charged parent ion ratio [BCE(2+)]/[BCE(+)] was measured, and the corresponding ionization process including non-sequential
R D Storer et al.
Carcinogenesis, 4(11), 1491-1494 (1983-11-01)
Hepatic DNA damage was demonstrated by alkaline DNA unwinding/hydroxylapatite batch chromatography in male B6C3F1 mice treated with non-necrogenic doses of 1,2-dichloroethane, 1-bromo-2-chloroethane, and 1,2-dibromoethane. Intraperitoneal administration of 0.5 mmol/kg of 1-bromo-2-chloroethane and 1,2-dibromoethane produced similar levels of DNA damage. A
J Plenge et al.
Physical chemistry chemical physics : PCCP, 13(19), 8705-8714 (2011-03-29)
We report on the coherent control of the ultrafast ionization and fragmentation dynamics of the bromochloroalkanes C(2)H(4)BrCl and C(3)H(6)BrCl using shaped femtosecond laser pulses. In closed-loop control experiments on bromochloropropane (C(3)H(6)BrCl) the fragment ion yields of CH(2)Cl(+), CH(2)Br(+), and C(3)H(3)(+)
Haiyan Wang et al.
Langmuir : the ACS journal of surfaces and colloids, 25(14), 8042-8050 (2009-04-21)
The conformational properties of 1-bromo-2-chloroethane (BCE) in several representative zeolites including silicalite-1, siliceous Y (Si-Y), Na-Y, and zeolite L have been investigated by FT-Raman spectroscopy in combination with thermogravimetric analysis. The results indicate that the conformational and dynamic behavior of
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