Allyl bromide | |
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1-Bromoprop-2-ene |
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Other names
Allyl bromide, 3-Bromopropene, 3-Bromopropylene, 3-Bromo-1-propene, Bromoallylene, 2-Propenyl bromide, UN 1099 |
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Identifiers | |
CAS number | 106-95-6 |
PubChem | 7841 |
ChemSpider | 7553 |
EC number | 203-446-6 |
RTECS number | UC7090000 |
Jmol-3D images | Image 1 Image 2 |
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Properties | |
Molecular formula | C3H5Br |
Molar mass | 120.99 g/mol |
Appearance | Clear to light yellow liquid |
Density | 1.398 g/cm3 |
Melting point |
-119 °C |
Boiling point |
71 °C |
Solubility in water | Very slightly soluble |
Hazards | |
MSDS | MSDS at Oxford University |
EU classification | Toxic (T), Flammable (F) |
R-phrases | R11, R25 |
S-phrases | S16, S28A, S29, S33, S36/37, S39, S45 |
NFPA 704 |
3
3
1
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Flash point | -2 - -1 °C |
Autoignition temperature |
280 °C |
Explosive limits | 4.3 - 7.3 % |
(verify) (what is: / ?) Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) |
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Infobox references |
Allyl bromide (1-bromoprop-2-ene) is an organic halide. Its refractive index is 1.4697 (20 °C, 589 nm). Allyl bromide is an alkylating agent used in synthesis of polymers, pharmaceuticals, allyls and other organic compounds. Physically, allyl bromide is a clear liquid with an intense, acrid, and persistent smell. In addition, allylzinc bromide may be produced by treating this compound with elemental zinc. Unlike most organometallic reagents, which are pyrophoric in air and destroyed by water, allylzinc bromide is stable in aqueous solvents and can attack aldehydes in a Barbier-type reaction, leading to carbon-carbon bond formation.