| Benzyl bromide[1] | |
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Bromomethylbenzene |
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| Identifiers | |
| CAS number | 100-39-0 |
| PubChem | 7498 |
| ChemSpider | 13851576 |
| ChEBI | CHEBI:59858 |
| ChEMBL | CHEMBL1085946 |
| Jmol-3D images | Image 1 Image 2 |
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| Properties | |
| Molecular formula | C7H7Br |
| Molar mass | 171.04 g/mol |
| Density | 1.438 g/cm³ at 20 °C |
| Melting point |
-3.9 °C, 269 K, 25 °F |
| Boiling point |
198-199 °C |
| (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 | |
Benzyl bromide, or α-bromotoluene, is an organic compound consisting of a benzene ring substituted with a bromomethyl group. It can be prepared by the bromination of toluene at room temperature in air, using manganese(IV) oxide as a heterogeneous catalyst. It is a colorless liquid that is decomposed slowly in water.
Benzyl bromide is used in organic synthesis for the introduction of the benzyl protecting group for alcohols and carboxylic acids.
Benzyl bromide is a strong lachrymator and is also intensely irritating to skin and mucous membranes. Because of these properties, it has been used as a war gas.
Benzyl bromide can be synthesized by the bromination of toluene under conditions suitable for a free radical halogenation:
N-Bromosuccinimide may also be used in place of elemental bromine.