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9-IODOPHENANTHRENE

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9-IODOPHENANTHRENE Basic information

Product Name:
9-IODOPHENANTHRENE
Synonyms:
  • 9-IODOPHENANTHRENE
  • 9-Iodophenanthrene 97%
  • 9-Phenanthryl iodide
  • 2,5-bis(4-ethoxyanilino)-3,6-dimethoxycyclohexa-2,5-diene-1,4-dione
  • Phenanthrene, 9-iodo-
CAS:
17024-12-3
MF:
C14H9I
MW:
304.13
Product Categories:
  • Aryl
  • C13 to C37+
  • Halogenated Hydrocarbons
Mol File:
17024-12-3.mol
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9-IODOPHENANTHRENE Chemical Properties

Melting point:
91-93 °C (lit.)
Boiling point:
411.0±14.0 °C(Predicted)
Density 
1.692±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
Appearance
Light yellow to yellow Solid
Stability:
Stable, but light sensitive - store in the dark. Incompatible with strong oxidizing agents.
InChI
InChI=1S/C14H9I/c15-14-9-10-5-1-2-6-11(10)12-7-3-4-8-13(12)14/h1-9H
InChIKey
CBFIPOTVFMLMFQ-UHFFFAOYSA-N
SMILES
C1=C2C(C3C(C(I)=C2)=CC=CC=3)=CC=C1
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3

MSDS

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9-IODOPHENANTHRENE Usage And Synthesis

Chemical Properties

solid

Synthesis

573-17-1

17024-12-3

General procedure for the synthesis of 9-iodophenanthrene from 9-bromophenanthrene: General method: aryl bromide (10 mmol) was dissolved in anhydrous THF (30 mL) and cooled to -78 °C at room temperature. Slowly add n-butyllithium (1.6 M, dissolved in hexane; 7.5 mL; 12 mmol) dropwise. After 15 min of reaction, a solution of anhydrous THF (10 mL) with iodine (I2, 3.81 g; 15 mmol) was added, followed by gradual warming of the reaction mixture to room temperature and stirring overnight. After completion of the reaction, the mixture was concentrated under vacuum. Water (H2O) was added to the residue and extracted with dichloromethane (DCM, 3 times). The organic phases were combined and washed sequentially with saturated sodium thiosulfate (Na2S2O5) solution and water. The organic phase was dried over anhydrous magnesium sulfate (MgSO4) and concentrated under reduced pressure, and the resulting crude product was purified by column chromatography.

References

[1] Synlett, 2013, vol. 24, # 20, p. 2730 - 2734
[2] Synthesis, 1986, # 1, p. 121 - 122
[3] Journal of Organic Chemistry, 2009, vol. 74, # 12, p. 4650 - 4653
[4] Tetrahedron Letters, 1999, vol. 40, # 36, p. 6671 - 6672
[5] Beilstein Journal of Organic Chemistry, 2011, vol. 7, p. 1499 - 1503

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