1-(2,4-dibromophenyl)ethanone
- Product Name
- 1-(2,4-dibromophenyl)ethanone
- CAS No.
- 33243-33-3
- Chemical Name
- 1-(2,4-dibromophenyl)ethanone
- Synonyms
- 1-(2,4-Dibromophenyl);2',4'-Dibromoacetophenone;Ethanone,1-(2,4-dibroMophenyl)-;1-(2,4-Dibromo-phenyl)-ethanone;1-(2,4-dibromophenyl)ethan-1-one;1-(2,4-Dibromophenyl)ethanone - [D92551]
- CBNumber
- CB52129593
- Molecular Formula
- C8H6Br2O
- Formula Weight
- 277.94
- MOL File
- 33243-33-3.mol
1-(2,4-dibromophenyl)ethanone Property
- Melting point:
- 61-62℃
- Boiling point:
- 316℃
- Density
- 1.812
- Flash point:
- 118℃
- storage temp.
- Sealed in dry,Room Temperature
- form
- Solid
- Appearance
- Light yellow to yellow Solid
Safety
- HS Code
- 2914500090
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H315Causes skin irritation
H319Causes serious eye irritation
H335May cause respiratory irritation
- Precautionary statements
-
P261Avoid breathing dust/fume/gas/mist/vapours/spray.
P304+P340IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
P405Store locked up.
N-Bromosuccinimide Price
- Product number
- FD70032
- Product name
- 2',4'-Dibromoacetophenone
- Packaging
- 2g
- Price
- $160
- Updated
- 2021/12/16
- Product number
- FD70032
- Product name
- 2',4'-Dibromoacetophenone
- Packaging
- 5G
- Price
- $275
- Updated
- 2021/12/16
- Product number
- FD70032
- Product name
- 2',4'-Dibromoacetophenone
- Packaging
- 10g
- Price
- $450
- Updated
- 2021/12/16
- Product number
- 3856AB
- Product name
- 1-(2,4-Dibromophenyl)ethanone
- Packaging
- 10g
- Price
- $651
- Updated
- 2021/12/16
- Product number
- OR471302
- Product name
- 2',4'-Dibromoacetophenone
- Packaging
- 1g
- Price
- $711
- Updated
- 2021/12/16
1-(2,4-dibromophenyl)ethanone Chemical Properties,Usage,Production
Synthesis
108-36-1
75-36-5
33243-33-3
Under argon protection, 1,3-dibromobenzene (4.1 g, 17.5 mmol) and anhydrous aluminum trichloride (5.6 g, 42 mmol) were placed in a 50 mL two-neck flask. Acetyl chloride (2.0 mL, 28 mmol) was slowly added dropwise at room temperature. After the dropwise addition, the reaction system was slowly heated to 100 °C, during which a large amount of hydrogen chloride gas was released. The reaction was maintained at this temperature for 1.5 hours. After completion of the reaction, the system was cooled to room temperature and slowly poured into a mixture of crushed ice and concentrated hydrochloric acid. The organic phase was separated and washed sequentially with water, sodium carbonate solution and brine. The organic phase was dried with anhydrous magnesium sulfate and evaporated under reduced pressure to remove the solvent. Finally, the target product 2',4'-dibromoacetophenone (4.5 g, 93% yield) was purified by column chromatography.
References
[1] Advanced Synthesis and Catalysis, 2016, vol. 358, # 6, p. 926 - 939
[2] Patent: CN106316958, 2017, A. Location in patent: Paragraph 0145; 0146; 0152; 0153
[3] Journal of the Chemical Society, 1949, p. 1133,1136
[4] Roczniki Chemii, 1973, vol. 47, p. 2333 - 2337
1-(2,4-dibromophenyl)ethanone Preparation Products And Raw materials
Raw materials
Preparation Products
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