Weight | 122.993 g/mol |
---|---|
Formula | C3H7Br |
Hydrogen Acceptors | 0 |
Hydrogen Donors | 0 |
Aromatic Rings | 0 |
Rotatable Bonds | 0 |
2-Bromopropane (75-26-3)
isopropyl bromide
Score:
#14 in Environmental health
,
#149 in Environmental science
,
#846 in Physics
,
#1975 in Biology
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- Hematopoietic and reproductive hazards of Korean electronic workers exposed to solvents containing 2-bromopropane (Scandinavian Journal of Work, Environment & Health, 1996)
- Kinetics and thermochemistry of R + hydrogen bromide .dblarw. RH + bromine atom reactions: determinations of the heat of formation of ethyl, isopropyl, sec-butyl and tert-butyl radicals (The Journal of Physical Chemistry, 1992)
- Testicular and Hematopoietic Toxicity of 2-Bromopropane, a Substitute for Ozone Layer-Depleting Chlorofluorocarbons (Journal of Occupational Health, 1997)
- An Outbreak of Hematopoietic and Reproductive Disorders Due to Solvents Containing 2-Bromopropane in an Electronic Factory, South Korea: Epidemiological Survey (Journal of Occupational Health, 1997)
- Long-term follow-up of abnormal spermatogenesis after exposure to solvent containing 2-bromopropane (Korea-Russia International Symposium on Science and Technology, 2003)
- Biochemical studies of toxic agents. The metabolism of 1- and 2-bromopropane in rats (Biochemical Journal, 1966)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H225: Highly Flammable liquid and vapor
Danger Flammable liquids - Category 2 - H360: May damage fertility or the unborn child
Danger Reproductive toxicity - Category 1A, 1B - H373: Causes damage to organs through prolonged or repeated exposure
Warning Specific target organ toxicity, repeated exposure - Category 2 - isopropyl bromide
-
SMILESCC(C)Br
-
InChIKeyNAMYKGVDVNBCFQ-UHFFFAOYSA-N
- Pubchem - 2-Bromopropane
- Wikipedia - 2-bromopropane
2-Bromopropane, also known as isopropyl bromide and 2-propyl bromide, is the halogenated hydrocarbon with the formula CH3CHBrCH3. It is a colorless liquid. It is used for introducing the isopropyl functional group in organic synthesis.
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