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4-AMINO-2,6-DIBROMOPHENOL

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4-AMINO-2,6-DIBROMOPHENOL Basic information

Product Name:
4-AMINO-2,6-DIBROMOPHENOL
Synonyms:
  • ASISCHEM U70323
  • 4-hydroxy-3,5-dibromoaniline
  • 4-amino-2,6-dibromo-pheno
  • Phenol, 4-amino-2,6-dibromo-
  • TIMTEC-BB SBB006577
  • 4-AMINO-2,6-DIBROMOPHENOL
  • 3,5-DIBROMO-4-HYDROXYANILINE
  • 2,6-DIBROMO-4-AMINOPHENOL
CAS:
609-21-2
MF:
C6H5Br2NO
MW:
266.92
EINECS:
210-185-1
Product Categories:
  • Building Blocks
  • C6 to C8
  • Phenol&Thiophenol&Mercaptan
  • Chemical Synthesis
  • Organic Building Blocks
  • Oxygen Compounds
  • Anilines, Amides & Amines
  • Bromine Compounds
  • Phenols
Mol File:
609-21-2.mol
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4-AMINO-2,6-DIBROMOPHENOL Chemical Properties

Melting point:
195-196 °C(lit.)
Boiling point:
295.6±40.0 °C(Predicted)
Density 
2.0444 (rough estimate)
refractive index 
1.6400 (estimate)
storage temp. 
2-8°C(protect from light)
pka
7.17±0.23(Predicted)
BRN 
2803732
CAS DataBase Reference
609-21-2(CAS DataBase Reference)
EPA Substance Registry System
Phenol, 4-amino-2,6-dibromo- (609-21-2)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-37/39-36
WGK Germany 
3
TSCA 
Yes
HazardClass 
IRRITANT
HS Code 
29222900

MSDS

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4-AMINO-2,6-DIBROMOPHENOL Usage And Synthesis

Chemical Properties

beige to pale brown crystalline powder

Synthesis

The synthesis of 4-amino-2,6-dibromophenol is as follows:4-Nitro-2,6-dibromophenol (2.97g, 10mmol) was dissolved in ethanol (15ml) and water (3ml), and acetic acid (1ml) was added. Then heat and stir to raise the temperature to 80°C, and add iron powder (1.68g, 30mmol) in batches. After the addition is complete, the reaction solution is kept warm for 30 minutes, heating is stopped, filtered while hot, the filtrate is concentrated under reduced pressure, then ethyl acetate and water are added to the concentrated residue to extract, the organic phases are combined and dried, filtered, and the solvent is removed under reduced pressure. The residue was finally separated by column chromatography (ethyl acetate/petroleum ether=1/3) to obtain 4-amino-2,6-dibromophenol (2.52g, 94.4% yield).
        

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