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9-Iodophenanthrene

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Company Name: Shanghai Fengtian Biotechnology Co., Ltd  Gold
Tel: 021-17514032201 17514032201
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Company Name: Beijing HwrkChemical Technology Co., Ltd  
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Company Name: BeiJing Hwrk Chemicals Limted  
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Company Name: Energy Chemical  
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Company Name: Shanghai Hanhong Scientific Co.,Ltd.  
Tel: 021-54306202 13764082696
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9-Iodophenanthrene manufacturers

9-Iodophenanthrene Basic information
Product Name:9-Iodophenanthrene
Synonyms:9-Iodophenanthrene 97%;9-Phenanthryl iodide;2,5-bis(4-ethoxyanilino)-3,6-dimethoxycyclohexa-2,5-diene-1,4-dione;Phenanthrene, 9-iodo-;9-IODOPHENANTHREN;9-Iodophenanthrene
CAS:17024-12-3
MF:C14H9I
MW:304.13
EINECS:
Product Categories:Aryl;C13 to C37+;Halogenated Hydrocarbons
Mol File:17024-12-3.mol
9-Iodophenanthrene Structure
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
AppearanceLight yellow to yellow Solid
Stability:Stable, but light sensitive - store in the dark. Incompatible with strong oxidizing agents.
InChIInChI=1S/C14H9I/c15-14-9-10-5-1-2-6-11(10)12-7-3-4-8-13(12)14/h1-9H
InChIKeyCBFIPOTVFMLMFQ-UHFFFAOYSA-N
SMILESC1=C2C(C3C(C(I)=C2)=CC=CC=3)=CC=C1
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36
WGK Germany 3
Storage Class11 - Combustible Solids
Hazard ClassificationsEye Irrit. 2
Skin Irrit. 2
STOT SE 3
MSDS Information
ProviderLanguage
SigmaAldrich English
9-Iodophenanthrene Usage And Synthesis
Chemical Propertiessolid
Synthesis
9-Bromophenanthrene

573-17-1

9-IODOPHENANTHRENE

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-Iodophenanthrene Preparation Products And Raw materials
Raw materials9-Bromophenanthrene-->Tetrahydrofuran-->n-Butyllithium-->iodine-->Hexane
Tag:9-Iodophenanthrene(17024-12-3) Related Product Information
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