Weight | 187.862 g/mol |
---|---|
Formula | C2H4Br2 |
Hydrogen Acceptors | 0 |
Hydrogen Donors | 0 |
Aromatic Rings | 0 |
Rotatable Bonds | 0 |
1,1-DIBROMOETHANE (557-91-5)
Score:
#1382 in Physics
,
#3219 in Biology
,
#4029 in Chemistry
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- Persistence of 1,2-dibromoethane in soils: entrapment in intraparticle micropores (Environmental Science & Technology, 1987)
- The role of glutathione conjugation in the mutagenicity of 1,2-dibromoethane (Biochemical Pharmacology, 1980)
- Evidence for formation of an S-[2-(N7-guanyl)ethyl]glutathione adduct in glutathione-mediated binding of the carcinogen 1,2-dibromoethane to DNA (Proceedings of the National Academy of Sciences of the United States of America, 1983)
- Macromolecular Binding and Metabolism of the Carcinogen 1,2-Dibromoethane (Cancer Research, 1978)
- S-[2-(N7-guanyl)ethyl]glutathione, the major DNA adduct formed from 1,2-dibromoethane. (Biochemistry, 1986)
- Genotoxic effects of 1,2-dibromoethane and 1,2-dichloroethane (Mutation Research\/reviews in Genetic Toxicology, 1980)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC(Br)Br
-
InChIKeyAPQIUTYORBAGEZ-UHFFFAOYSA-N
- Pubchem - 1,1-DIBROMOETHANE
- Wikipedia - 1,1-dibromoethane
1,1-Dibromoethane is a clear, slightly brown, flammable chemical compound. It is classified as the organobromine compound, and has the chemical formula C2H4Br2 and it is a position isomer of 1,2-Dibromoethane. It is commonly seen in the industrial chemistry, where it is used as fuels or fuel additives.
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