ChemicalBook--->CAS DataBase List--->57103-21-6

57103-21-6

57103-21-6 Structure

57103-21-6 Structure
IdentificationBack Directory
[Name]

3,6-DIIODO-9-PHENYL-9H-CARBAZOLE
[CAS]

57103-21-6
[Synonyms]

3,6-Diiodo-9-phenylcarbazole
3,6-Diiodo-9-phenylcarbazole>
3,6-DIIODO-9-PHENYL-9H-CARBAZOLE
9H-Carbazole,3,6-diiodo-9-phenyl
[Molecular Formula]

C18H11I2N
[MDL Number]

MFCD11521285
[MOL File]

57103-21-6.mol
[Molecular Weight]

495.1
Chemical PropertiesBack Directory
[Melting point ]

181.0 to 185.0 °C
[Boiling point ]

540.8±43.0 °C(Predicted)
[density ]

1.94±0.1 g/cm3(Temp: 20 °C; Press: 760 Torr)(Predicted)
[storage temp. ]

Keep in dark place,Sealed in dry,Room Temperature
[solubility ]

slightly sol. in dichloromethane
[form ]

powder to crystal
[color ]

White to Light yellow to Light orange
[CAS DataBase Reference]

57103-21-6
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[HS Code ]

2933.99.8290
Spectrum DetailBack Directory
[Spectrum Detail]

3,6-DIIODO-9-PHENYL-9H-CARBAZOLE(57103-21-6)1HNMR
Hazard InformationBack Directory
[Synthesis]

N-PHENYLCARBAZOLE HYDROCHLORIDE

1150-62-5

3,6-DIIODO-9-PHENYL-9H-CARBAZOLE

57103-21-6

The general procedure for the synthesis of 3,6-diiodo-9-phenylcarbazole from N-phenylcarbazole was as follows: first, 24.3 g (100 mmol) of 9-phenylcarbazole was dissolved in 700 mL of glacial acetic acid, followed by the slow addition of 44.9 g (200 mmol) of N-iodosuccinimide. The reaction mixture was stirred at room temperature overnight. Upon completion of the reaction, the resulting precipitate was collected by filtration and the residue was washed sequentially with saturated aqueous sodium bicarbonate solution, water and methanol and finally dried. 47.0 g (95% yield) of the target product 3,6-diiodo-9-phenylcarbazole was obtained as a white powder.

[References]

[1] Patent: WO2006/70912, 2006, A1. Location in patent: Page/Page column 58; 59
[2] Patent: WO2006/43647, 2006, A1. Location in patent: Page/Page column 59-60
[3] Patent: WO2012/25510, 2012, A1. Location in patent: Page/Page column 23
[4] Patent: EP2433928, 2012, A1. Location in patent: Page/Page column 16-17
[5] Journal of Chemical Research, 2017, vol. 41, # 2, p. 79 - 81
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