1,10-Phenanthroline, 4,7-dibroMo-
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
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
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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1,10-Phenanthroline, 4,7-dibroMo-(156492-30-7)Related Product Information
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