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53631-13-3

53631-13-3 Structure

53631-13-3 Structure
IdentificationBack Directory
[Name]

Ethanone, 2-broMo-1-(3,5-dichlorophenyl)- (Related Reference)
[CAS]

53631-13-3
[Synonyms]

2-Bromo-3',5'-dichloroacetophenone
2-bromo-1-(3,5-dichlorophenyl)ethan-1-one
Ethanone, 2-bromo-1-(3,5-dichlorophenyl)-
Ethanone, 2-broMo-1-(3,5-dichlorophenyl)- (Related Reference)
[Molecular Formula]

C8H5BrCl2O
[MDL Number]

MFCD03425180
[MOL File]

53631-13-3.mol
[Molecular Weight]

267.93
Chemical PropertiesBack Directory
[Boiling point ]

334.1±37.0 °C(Predicted)
[density ]

1.695±0.06 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[Appearance]

White to off-white Solid
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H317-H319
[Precautionary statements ]

P280-P305+P351+P338
Hazard InformationBack Directory
[Uses]

2-Bromo-1-(3,5-dichlorophenyl)ethanone is used in the synthesis of a new group of fungicides.
[Synthesis]

3',5'-Dichloroacetophenone

14401-72-0

Ethanone, 2-broMo-1-(3,5-dichlorophenyl)- (Related Reference)

53631-13-3

i) Synthesis of 2-bromo-1-(3,5-dichlorophenyl)-1-ethanone: 1.03 mL (0.02 mol) of bromine was added dropwise to a 50 mL solution of acetic acid containing 3.77 g (0.019 mol) of 1-(3,5-dichlorophenyl)ethanone at room temperature. The reaction mixture was stirred continuously at room temperature for 12 hours. Upon completion of the reaction, the acetic acid was removed by distillation under reduced pressure to give a yellow solid precipitate, the target product 2-bromo-1-(3,5-dichlorophenyl)-1-ethanone in 81% yield.

[References]

[1] Patent: US5945382, 1999, A
[2] Patent: CN105315279, 2016, A. Location in patent: Paragraph 0144
Spectrum DetailBack Directory
[Spectrum Detail]

Ethanone, 2-broMo-1-(3,5-dichlorophenyl)- (Related Reference)(53631-13-3)1HNMR
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