Phenacyl bromide
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Names | |
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Preferred IUPAC name
2-Bromo-1-phenylethan-1-one | |
Other names
2-Bromo-1-phenylethanone
2-Bromoacetophenone α-Bromoacetophenone Bromomethyl phenyl ketone | |
Identifiers | |
3D model (JSmol)
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ChEBI | |
ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.000.659 ![]() |
PubChem CID
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UNII | |
CompTox Dashboard (EPA)
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Properties | |
C8H7BrO | |
Molar mass | 199.047 g·mol−1 |
Appearance | Colorless solid |
Melting point | 50 °C (122 °F; 323 K)[1] |
Boiling point | 136 °C (277 °F; 409 K) 18 mm Hg[1] |
Hazards | |
Main hazards | Toxic(T) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
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Infobox references | |
Phenacyl bromide is the organic compound with the formula C6H5C(O)CH2Br. This colourless solid is a powerful lachrymator as well as a useful precursor to other organic compounds.
It is prepared by bromination of acetophenone:[2]
- C6H5C(O)CH3 + Br2 → C6H5C(O)CH2Br + HBr
The compound was first reported in 1871.[3]
References[]
- ^ Jump up to: a b Phenacyl Bromide, TCI America
- ^ R. M. Cowper and L. H. Davidson. "Phenacyl bromide". Organic Syntheses.; Collective Volume, 2, p. 480
- ^ A. Emmerling and C. Engler (1871). "Ueber einige Abkömmlinge des Acetophenons". Ber. 4 (1): 147–149. doi:10.1002/cber.18710040149.
External links[]
Media related to Phenacyl bromide at Wikimedia Commons
Categories:
- Lachrymatory agents
- Organobromides
- Organohalide stubs