74294
Chloroethane
≥99.8%
Synonym(s):
Ethyl chloride
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About This Item
Empirical Formula (Hill Notation):
C2H5Cl
CAS Number:
Molecular Weight:
64.51
EC Number:
200-830-5
UNSPSC Code:
12142100
PubChem Substance ID:
Beilstein/REAXYS Number:
1730751
MDL number:
Assay:
≥99.8%
InChI key
HRYZWHHZPQKTII-UHFFFAOYSA-N
InChI
1S/C2H5Cl/c1-2-3/h2H2,1H3
SMILES string
CCCl
vapor density
2.22 (vs air)
vapor pressure
19.2 psi ( 20 °C)
assay
≥99.8%
impurities
≤0.02% water
bp
12.3 °C (lit.)
mp
−139 °C (lit.)
density
0.921 g/mL at 0-4 °C (lit.)
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General description
Chloroethane is a haloalkane used as an intermediate or as a solvent in organic synthesis. It has major applications in the production of tetraethyl lead, ethyl-cellulose, and an antiknock additive for gasoline. It is also used in cleaning and degreasing applications.
Application
Chloroethane can be used to prepare:
- pyrido[1,2-a]pyrimidinone derivatives
- 2H-perovskite compound [Me3NCH2CH3]CdCl3
- benzo[cd]indol-2(1H)-ones derivatives as potent BRD4 inhibitors
Packaging
cylinder with 11.4 kg (net)
Regulatory Information
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Selective formation of chloroethane by the hydrochlorination of ethene using zinc catalysts
Conte M, et al.
J. Catal., 252(1), 23-29 (2007)
Reversible high temperature dielectric switching in a 2 H-perovskite compound:[Me 3 NCH 2 CH 3] CdCl 3
Sun D, et al.
CrystEngComm, 21(16), 2669-2674 (2019)
Design, synthesis and biological evaluation of benzo [cd] indol-2 (1H)-ones derivatives as BRD4 inhibitors
Feng Y, et al.
European Journal of Medicinal Chemistry, 152(16), 264-273 (2018)
First discovery of novel pyrido [1,2-a] pyrimidinone mesoionic compounds as antibacterial agents
Liu D, et al.
Journal of Agricultural and Food Chemistry, 67(43), 11860-11866 (2019)
Andreas Tiehm et al.
Current opinion in biotechnology, 22(3), 415-421 (2011-03-08)
Because of a range of different industrial activities, sites contaminated with chloroethenes are a world-wide problem. Chloroethenes can be biodegraded by reductive dechlorination under anaerobic conditions as well as by oxidation under aerobic conditions. The tendency of chloroethenes to undergo
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