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2,5-Dibromoterephthalaldehyde

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2,5-Dibromoterephthalaldehyde Basic information

Product Name:
2,5-Dibromoterephthalaldehyde
Synonyms:
  • 2,5-Dibromoterephthalaldehyde
  • MiniMuM x 1 or 1g x 1, 5g x 1
  • 2,5-DIBROMO-1,4-BENZENEDICARBOXALDEHYDE
  • 2,5-Dibromo-1,4-dicarbaldehyde
  • 2,5-Dibromobenzene-1,4-dicarbaldehyde
  • 2,5-Dibromo-1,4-diformylbenzene
  • 1,4-Benzenedicarboxaldehyde, 2,5-dibromo-
  • 2,5-DIBROMO-1,4-BENZENEDICARBOXALDEHYDE ISO 9001:2015 REACH
CAS:
63525-48-4
MF:
C8H4Br2O2
MW:
291.92
Mol File:
63525-48-4.mol
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2,5-Dibromoterephthalaldehyde Chemical Properties

Melting point:
189 °C
Boiling point:
357.4±42.0 °C(Predicted)
Density 
2.011
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
form 
powder to crystal
color 
White to Green to Brown
InChI
InChI=1S/C8H4Br2O2/c9-7-1-5(3-11)8(10)2-6(7)4-12/h1-4H
InChIKey
VSUKSWCSOBXUFG-UHFFFAOYSA-N
SMILES
C1(C=O)=CC(Br)=C(C=O)C=C1Br
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Safety Information

HS Code 
2913.00.4000
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2,5-Dibromoterephthalaldehyde Usage And Synthesis

Uses

2,5-Dibromoterephthalaldehyde is an organic compound, mainly used as an organic synthesis intermediate and pharmaceutical intermediate, and is widely used in laboratory research and development processes and chemical production processes.

Synthesis

36711-69-0

63525-48-4

GENERAL METHOD: Compound 2d (302 mg, 0.516 mmol) was dissolved in ethanol (10 mL), followed by the addition of an aqueous (4 mL) solution of silver nitrate (369 mg, 2.17 mmol). The reaction mixture was heated to reflux for 40 min under argon protection. Upon completion of the reaction, the solution was allowed to cool to room temperature, the resulting silver bromide precipitate was removed by filtration, and the precipitate was washed with ethanol (2 x 5 mL). After removal of the solvent by evaporation, the residue was purified by recrystallization (solvent hexane) to give the target product 3d (146 mg, 94% yield) as a white solid.

References

[1] Angewandte Chemie - International Edition, 2014, vol. 53, # 26, p. 6786 - 6790
[2] Angew. Chem., 2014, vol. 126, # 26, p. 6904 - 6908,5
[3] Synthesis (Germany), 2016, vol. 48, # 20, p. 3509 - 3514
[4] Chemical Communications, 2017, vol. 53, # 53, p. 7266 - 7269
[5] Helvetica Chimica Acta, 1944, vol. 27, p. 274,290

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