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2-Chloro-4-bromobenzaldehyde

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2-Chloro-4-bromobenzaldehyde Basic information

Product Name:
2-Chloro-4-bromobenzaldehyde
Synonyms:
  • 4-BROMO-2-CHLOROBENZALDEHYDE
  • 2-Chloro-4-bromobenzaldehyde
  • Chloro-4-bromobenzaldehyde
  • Benzaldehyde,4-broMo-2-chloro-
  • 2-Chloro-4-broMobenzaldehyde, 95+%
  • 4-Bromo-2-chlorobenzaldehyde >
  • 2-Chloro-4-bromobenzaldehyde, 97%min
CAS:
158435-41-7
MF:
C7H4BrClO
MW:
219.46
Product Categories:
  • Adehydes, Acetals & Ketones
  • Bromine Compounds
  • Chlorine Compounds
Mol File:
158435-41-7.mol
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2-Chloro-4-bromobenzaldehyde Chemical Properties

Melting point:
74-76℃
Boiling point:
271.3±25.0 °C(Predicted)
Density 
1.698±0.06 g/cm3(Predicted)
storage temp. 
Inert atmosphere,2-8°C
solubility 
soluble in Methanol
form 
powder to crystal
color 
White to Orange to Green
Sensitive 
Air Sensitive
CAS DataBase Reference
158435-41-7(CAS DataBase Reference)
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Safety Information

Hazard Codes 
C,Xn
Risk Statements 
22
Hazard Note 
Corrosive
HS Code 
2913000090
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2-Chloro-4-bromobenzaldehyde Usage And Synthesis

Chemical Properties

Light yellow crystalline powder

Uses

4-Bromo-2-chlorobenzaldehyde is a useful research chemical for organic synthesis and other chemical processes.4-Bromo-2-chlorobenzaldehyde is used in preparation of Heterocyclic compounds as P2X3 antagonist and its intermediate.

Synthesis

185315-48-4

158435-41-7

General procedure for the synthesis of 2-chloro-4-bromobenzaldehyde from (4-bromo-2-chlorophenyl)methanol: Oxalyl chloride (6.9 g, 54 mmol, 1.3 eq.) was dissolved in dichloromethane (DCM, 153 mL) and the solution was cooled to -78 °C. A solution of DCM (57 mL) in dimethyl sulfoxide (DMSO, 4.72 mL, 66.5 mmol, 1.6 eq.) was slowly added dropwise to the cooled solution at -78 °C and stirred for 15 min. (4-Bromo-2-chlorophenyl)methanol (Compound 43, 9.2 g, 41.5 mmol, 1.0 eq.) was dissolved in DCM (116 mL) and added drop-wise to the above cooled solution, keeping the temperature at -78 °C. Stirring was continued at -78 °C for 2 hours. Subsequently, triethylamine (TEA, 28.7 mL, 207 mmol, 5 eq.) was added to slowly warm the reaction mixture to room temperature. After stirring for 30 min at room temperature, the reaction mixture was diluted with DCM (300 mL), washed sequentially with saturated ammonium chloride (NH4Cl) solution and brine, dried with anhydrous sodium sulfate (Na2SO4), filtered and concentrated in vacuum to afford 2-chloro-4-bromobenzaldehyde (Compound 44) in 96% yield (8.8 g).

References

[1] Patent: WO2008/51826, 2008, A2. Location in patent: Page/Page column 53; 54
[2] Patent: WO2008/103277, 2008, A2. Location in patent: Page/Page column 197
[3] Journal of Medicinal Chemistry, 2017, vol. 60, # 18, p. 7820 - 7834
[4] Patent: WO2013/75083, 2013, A1. Location in patent: Paragraph 006309; 00632
[5] Patent: US9206128, 2015, B2. Location in patent: Page/Page column 275; 276; 277

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