Basic information Safety Supplier Related

1,10-Phenanthroline, 4,7-dibroMo-

Basic information Safety Supplier Related

1,10-Phenanthroline, 4,7-dibroMo- Basic information

Product Name:
1,10-Phenanthroline, 4,7-dibroMo-
Synonyms:
  • 1,10-Phenanthroline, 4,7-dibroMo-
  • 4,7-DibroMophenanthroline
  • 4,7-Dibromo-1,10-phenanthroline Hydrate
  • 1,10-Phenthroline, 4,7-dibroMo-
  • 4,7-dibromo
  • 4,7-dibromo-1,1-phenanthroline
CAS:
156492-30-7
MF:
C12H6Br2N2
MW:
338
EINECS:
1592732-453-0
Mol File:
156492-30-7.mol
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1,10-Phenanthroline, 4,7-dibroMo- Chemical Properties

Melting point:
236℃
Boiling point:
466.6±40.0 °C(Predicted)
Density 
1.915±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
form 
powder to crystal
pka
3.29±0.10(Predicted)
color 
White to Yellow
InChI
InChI=1S/C12H6Br2N2/c13-9-3-5-15-11-7(9)1-2-8-10(14)4-6-16-12(8)11/h1-6H
InChIKey
AKZAIDYHEKUXBU-UHFFFAOYSA-N
SMILES
N1C2C(=CC=C3C=2N=CC=C3Br)C(Br)=CC=1
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Safety Information

HS Code 
2933.99.8290
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1,10-Phenanthroline, 4,7-dibroMo- Usage And Synthesis

Synthesis

87330-27-6

156492-30-7

1,10-Phenanthroline-4,7(1H,10H)-dione (73c, 4.2 g, 20 mmol) was used as a feedstock and mixed with tribromophosphine (14.3 g, 50 mmol) in anhydrous chloroform. The reaction mixture was refluxed for 6 hours under nitrogen protection. Upon completion of the reaction, the reaction solution was washed with water followed by saturated brine three times. The organic layer was dried with anhydrous magnesium sulfate and the solvent was removed by evaporation. Finally, the crude product was purified by silica gel column chromatography to afford 4,7-dibromo-1,10-phenanthroline (73d, 4.7 g, 13.9 mmol) in 70% yield.

References

[1] Patent: CN106831743, 2017, A. Location in patent: Paragraph 0129; 0134; 0135
[2] Journal of Organic Chemistry, 1951, vol. 16, p. 941,945
[3] Tetrahedron, 2002, vol. 58, # 44, p. 9095 - 9100

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