Weight | 201.889 g/mol |
---|---|
Formula | C3H6Br2 |
Hydrogen Acceptors | 0 |
Hydrogen Donors | 0 |
Aromatic Rings | 0 |
Rotatable Bonds | 2 |
1,3-DIBROMOPROPANE (109-64-8)
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- Identification and quantitative determination of four different mercapturic acids formed from 1,3-dibromopropane and its 1,1,3,3-tetradeutero analogue by the rat (Xenobiotica, 1986)
- Reaction of 5,5-diphenyl-2-thiohydantoin with 1,3-dibromopropane under phase transfer catalytic conditions : Crystal and molecular structure of 2,3,4,5-tetrahydro-7,7-diphenylimidazo-[2,1-b]-thiazine -6(7H)-one (Tetrahedron, 1981)
- Reaction of 5,5-diphenyl-2-thiohydantoin with 1,3-dibromopropane : Crystal and molecular structure of 2,3,4,5-tetrahydro-6,6-diphenylimidazo [2, 1-b]-thiazine-7 (6H)-one (Tetrahedron, 1980)
- The molecular structure, conformations and vibrational spectra of 2,2-di(chloromethyl)-1,3-dichloropropane and 2,2-di(bromomethyl)-1,3-dibromopropane (Journal of Molecular Structure, 1986)
- Conformational Analysis. V. The Molecular Structure, Torsional Oscillations, and Conformational Equilibria of Gaseous 1,3-Dibromopropane, (CH2Br)2CH2, as Determined by Electron Diffraction and Compared with Semi-empirical (Molecular Mechanics) Calculations. (Acta Chemica Scandinavica, 1974)
- Reactivity of ,-dibromoalkanes at copper and silver cathodes: (I) Behaviour of 1,3-dibromopropane (Journal of Electroanalytical Chemistry, 2009)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H226: Flammable liquid and vapor
Warning Flammable liquids - Category 3 - H373: Causes damage to organs through prolonged or repeated exposure
Warning Specific target organ toxicity, repeated exposure - Category 2 - H411: Toxic to aquatic life with long lasting effects
Hazardous to the aquatic environment, long-term hazard - Category 2 -
SMILESC(CBr)CBr
-
InChIKeyVEFLKXRACNJHOV-UHFFFAOYSA-N
- Pubchem - 1,3-DIBROMOPROPANE
- Wikipedia - trimethylene bromide
1,3-Dibromopropane is a halogenated hydrocarbon. When at room temperature, it is a colorless to light-brown liquid containing sweet odor. Synthetically, it is very useful to form C3-bridged compounds such as through C-N coupling reactions.
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