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232750

Sigma-Aldrich

1-Brom-2-chlorethan

98%

Synonym(e):

Ethylenbromchlorid, Ethylenchlorbromid

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About This Item

Lineare Formel:
ClCH2CH2Br
CAS-Nummer:
107-04-0
Molekulargewicht:
143.41
Beilstein:
605265
EG-Nummer:
203-456-0
MDL-Nummer:
MFCD00000962
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24853925
NACRES:
NA.22

Qualitätsniveau

200

Assay

98%

Form

liquid

Brechungsindex

n20/D 1.488 (lit.)

bp

106-107 °C (lit.)

mp (Schmelzpunkt)

−18-−14 °C (lit.)

Löslichkeit

water: soluble

Dichte

1.723 g/mL at 25 °C (lit.)

Funktionelle Gruppe

bromo
chloro

SMILES String

ClCCBr

InChI

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

InChIKey

IBYHHJPAARCAIE-UHFFFAOYSA-N

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Allgemeine Beschreibung

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.

Anwendung

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

Piktogramme

Skull and crossbonesHealth hazard
GHS06,GHS08

Signalwort

Danger

Gefahreneinstufungen

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

Zielorgane

Respiratory system

Lagerklassenschlüssel

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

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

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

Hier finden Sie alle aktuellen Versionen:

Analysenzertifikate (COA)

Lot/Batch Number
SDBB0837
STBK9633
BCCF3165
BCCC1146
BCBQ8054V

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1,2-Dibromethan ≥99%

Sigma-Aldrich

240656

1,2-Dibromethan

Bromchlormethan contains 100 ppm BHT as inhibitor, ≥99.5%

Sigma-Aldrich

135267

Bromchlormethan

2-Chlorethanol 99%

Sigma-Aldrich

185744

2-Chlorethanol

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
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
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.
L A Ballering et al.
Mutation research, 285(2), 209-217 (1993-02-01)
The genetic activity profiles of three structurally related dihaloalkanes, 1,2-dibromoethane (DBE), 1,2-dichloroethane (DCE) and 1-bromo-2-chloroethane (BCE), were compared in germ cells and somatic tissue of Drosophila melanogaster. The two genotoxicity indices estimated after mutagen exposure of male germ cells were
Irina Yankelzon et al.
Environmental science and pollution research international, 27(18), 22749-22757 (2020-04-24)
Multi-elemental C-Br-Cl compound-specific isotope analysis was applied for characterizing abiotic and biotic degradation of the environmental pollutant 1-bromo-2-chloroethane (BCE). Isotope effects were determined in the model processes following hydrolytic dehalogenation and dihaloelimination pathways as well as in a microcosm experiment
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