Basic information Safety Supplier Related

2-Chloro-4-bromoacetophenone

Basic information Safety Supplier Related

2-Chloro-4-bromoacetophenone Basic information

Product Name:
2-Chloro-4-bromoacetophenone
Synonyms:
  • 2'-Chloro-4'-bromoacetophenone 97%
  • 2-CHLORO-4-BROMOACETOPHENONE 99+%
  • 1-(4-bromo-2-chlorophenyl)ethanone
  • 4-Bromo-6-chloroacetophenone
  • Ethanone, 1-(4-bromo-2-chlorophenyl)-
  • -bromoacetophenone
  • -Chloro-4&rsquo
  • 1-(4-bromo-2-chlorophenyl)ethan-1-one
CAS:
252561-81-2
MF:
C8H6BrClO
MW:
233.49
Product Categories:
  • Adehydes, Acetals & Ketones
  • Bromine Compounds
  • Chlorine Compounds
Mol File:
252561-81-2.mol
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2-Chloro-4-bromoacetophenone Chemical Properties

Boiling point:
265.6±25.0 °C(Predicted)
Density 
1.566±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
form 
solid
color 
Yellow
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Safety Information

Hazard Codes 
Xn
HS Code 
2914790090
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2-Chloro-4-bromoacetophenone Usage And Synthesis

Uses

2''-Chloro-4''-bromoacetophenone

Synthesis

875306-64-2

252561-81-2

Step 6-J: Methylmagnesium bromide (44 mL, 61.6 mmol, 1.4 M in tetrahydrofuran) was slowly added dropwise to tetrahydrofuran (50 mL) at -78 °C. Subsequently, a solution consisting of 4-bromo-2-chloro-N-methoxy-N-methylbenzamide (3.52 g, 12.7 mmol, from Step 6-I) dissolved in tetrahydrofuran (30 mL) was added. The reaction mixture was stirred at -78°C for 45 minutes, then brought to room temperature and continued stirring for 1.5 hours. After completion of the reaction, the mixture was extracted with ethyl acetate (3 times), the organic phases were combined, washed with brine, dried over anhydrous sodium sulfate, filtered and concentrated in vacuum. The crude product was purified by recrystallization (solvent: ethyl acetate/hexane) to afford 1-(4-bromo-2-chlorophenyl)ethanone as a white solid (1.1 g, 37% yield).

References

[1] Patent: US2009/170920, 2009, A1. Location in patent: Page/Page column 13-14
[2] Patent: JP2015/231988, 2015, A

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