| Weight | 198.274 g/mol |
|---|---|
| Formula | CBrCl3 |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
BROMOTRICHLOROMETHANE (75-62-7)
Trichlorobromomethane
Score:
#971 in Biochemistry
,
#1118 in Physics
,
#3188 in Chemistry
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LabBot
- Bioactivation of carbon tetrachloride, chloroform and bromotrichloromethane: Role of cytochrome P-450 (Life Sciences, 1977)
- Spin-trapping of the trichloromethyl radical produced during enzymic NADPH oxidation in the presence of carbon tetrachloride or bromotrichloromethane (Biochimica et Biophysica Acta, 1978)
- Destruction of liver microsomal calcium pump activity by carbon tetrachloride and bromotrichloromethane (Biochemical Pharmacology, 1981)
- The formation of diglutathionyl dithiocarbonate as a metabolite of chloroform, bromotrichloromethane, and carbon tetrachloride. (Drug Metabolism and Disposition, 1981)
- Carbon tetrachloride, bromotrichloromethane and ethanol acute intoxication. New chemical evidence for lipid peroxidation in rat tissue microsomes. (Biochemical Journal, 1983)
- Hepatotoxicity of bromotrichloromethane bond dissociation energy and lipoperoxidation (Biochemical Pharmacology, 1974)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Trichlorobromomethane
-
SMILESC(Cl)(Cl)(Cl)Br
-
InChIKeyXNNQFQFUQLJSQT-UHFFFAOYSA-N
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Synthesis
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BROMOTRICHLOROMETHANE
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