Acetyl bromide
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Names | |||
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Preferred IUPAC name
Acetyl bromide | |||
Identifiers | |||
3D model (JSmol)
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ChemSpider | |||
ECHA InfoCard | 100.007.329 | ||
EC Number |
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PubChem CID
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RTECS number |
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UNII | |||
UN number | 1716 | ||
CompTox Dashboard (EPA)
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Properties | |||
C2H3BrO | |||
Molar mass | 122.949 g·mol−1 | ||
Density | 1.663 g/mL | ||
Melting point | −96 °C (−141 °F; 177 K) | ||
Boiling point | 75 to 77 °C (167 to 171 °F; 348 to 350 K) | ||
Hazards | |||
Safety data sheet | ILO MSDS | ||
GHS labelling: | |||
Signal word
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Danger | ||
H314 | |||
P260, P264, P280, P301+P330+P331, P303+P361+P353, P304+P340, P305+P351+P338, P310, P321, P363, P405, P501 | |||
Flash point | 110 °C (230 °F; 383 K) | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |||
what is ?) | (|||
Infobox references | |||
Acetyl bromide is an acyl bromide compound. As is expected, it may be prepared by reaction between phosphorus tribromide and acetic acid:[2]
- 3 CH3COOH + PBr3 → 3 CH3COBr + H3PO3
As usual for an acid halide, acetyl bromide hydrolyzes rapidly in water, forming acetic acid and hydrobromic acid. It also reacts with alcohols and amines to produce acetate esters and acetamides, respectively.
References[]
- ^ Acetyl bromide[permanent dead link] at Sigma-Aldrich
- ^ Theodore M. Burton and Ed. F. Degering (1940). "The Preparation of Acetyl Bromide". J. Am. Chem. Soc. 62: 227. doi:10.1021/ja01858a502.
Categories:
- Acyl bromides
- Organic compound stubs