9-IODOPHENANTHRENE
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
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
MSDS
- Language:English Provider:SigmaAldrich
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
9-IODOPHENANTHRENESupplier
- Tel
- 021-17514032201 17514032201
- 17514032201@163.com
- Tel
- 18515581800 18501085097
- sales.bj@hwrkchemical.com
- Tel
- 0757-86329057 18934348241
- sales4.gd@hwrkchemical.com
- Tel
- 021-021-58432009 400-005-6266
- sales8178@energy-chemical.com
- Tel
- 021-54306202 13764082696
- info@hanhongsci.com