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3-BROMO-5-CHLORO-BENZALDEHYDE

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3-BROMO-5-CHLORO-BENZALDEHYDE Basic information

Product Name:
3-BROMO-5-CHLORO-BENZALDEHYDE
Synonyms:
  • 3-BROMO-5-CHLORO-BENZALDEHYDE
  • 3-Bromo-5-chlorobenzladehyde
  • 5-Chloro-3-bromobenzaldehyde
  • 3-BroMo-5-chlorobenzaldehyde, 98%+
  • 3-Bromo-5-chL
  • Benzaldehyde, 3-bromo-5-chloro-
  • CAS:188813-05-0
CAS:
188813-05-0
MF:
C7H4BrClO
MW:
219.46
Product Categories:
  • C7Chemical Synthesis
  • Aldehydes
  • Carbonyl Compounds
  • New Products for Chemical Synthesis
  • Organic Building Blocks
Mol File:
188813-05-0.mol
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3-BROMO-5-CHLORO-BENZALDEHYDE Chemical Properties

Melting point:
68-73 °C
Boiling point:
264.0±20.0 °C(Predicted)
Density 
1.698±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
solubility 
soluble in Methanol
form 
powder to crystal
color 
White to Light yellow
InChI
InChI=1S/C7H4BrClO/c8-6-1-5(4-10)2-7(9)3-6/h1-4H
InChIKey
JGMGDYUVFBBCEQ-UHFFFAOYSA-N
SMILES
C(=O)C1=CC(Cl)=CC(Br)=C1
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Safety Information

Hazard Codes 
Xn,N
Risk Statements 
36/37/38-51/53-22
Safety Statements 
26-36/37/39-61-53
RIDADR 
UN 3077 9/PG 3
WGK Germany 
3
HS Code 
2913000090
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3-BROMO-5-CHLORO-BENZALDEHYDE Usage And Synthesis

Chemical Properties

white crystal powder

Synthesis

14862-52-3

68-12-2

188813-05-0

Under nitrogen protection, 3,5-dibromochlorobenzene (27 g, 100 mmol) was dissolved in anhydrous isopropyl ether (300.0 mL) in a dry flask. The reaction mixture was cooled to -78 °C and stirred continuously under nitrogen atmosphere. A 2.6 M hexane solution of n-butyllithium (40 mL, 100 mmol) was slowly added dropwise to the above solution. After the dropwise addition was completed, the reaction mixture was continued to be stirred at -78 °C for 30 minutes. Subsequently, N,N-dimethylformamide (DMF, 7.5 g, 100 mmol) was added dropwise while keeping the temperature below -78 °C. After the reaction was completed, 80 mL of ammonium chloride solution was added to the mixture and stirring was continued for 15 minutes. The ether layer was separated, washed sequentially with water (2 x 250 mL), dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. Finally, the crude product was purified by silica gel fast column chromatography to afford the target compound 3-bromo-5-chlorobenzaldehyde (16 g, 67% yield).

References

[1] Patent: WO2014/15054, 2014, A1. Location in patent: Page/Page column 174; 190

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