3-Iodo-N-phenylcarbazole CAS 502161-03-7

Introduction:Basic information about 3-Iodo-N-phenylcarbazole CAS 502161-03-7, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

3-Iodo-N-phenylcarbazole Basic information

Product Name:3-Iodo-N-phenylcarbazole
Synonyms:3-Iodo-N-phenylcarbazole;3-Iodo-9-phenylcarbazole;3-iodo-9-phenyl-9H-carbazole;3-iodo-N-phenylcarbazol;3-Iodo-N-phenylcarba;3-iodo-9-phenylcarbazole,3-Iodo-9-phenylcarbazole;3-Iodo-9-phenylcarbazole/3-Iodo-N-phenylcarbazole;3- iodine-9- phenylcarbazole
CAS:502161-03-7
MF:C18H12IN
MW:369.2
EINECS:808-151-1
Product Categories:OLED materials,pharm chemical,electronic;API intermediates
Mol File:502161-03-7.mol

3-Iodo-N-phenylcarbazole Chemical Properties

Melting point 103.0 to 107.0 °C
Boiling point 480.6±27.0 °C(Predicted)
density 1.55±0.1 g/cm3(Predicted)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
form powder to crystal
color White to Light yellow
CAS DataBase Reference502161-03-7

Safety Information

HS Code 2933998090

3-Iodo-N-phenylcarbazole Usage And Synthesis

Chemical PropertiesWhite crystalline powder
Synthesis

1150-62-5

502161-03-7

General procedure for the synthesis of 3-iodo-9-phenylcarbazole from N-phenylcarbazole: 2.433 g (10 mmol) of intermediate compound A (N-phenylcarbazole) was dissolved in 100 mL of 80% acetic acid solution, followed by the sequential addition of 1.357 g (5.35 mmol) of iodine monomers (I2) and 0.333 g (1.46 mmol) of o-n-octanoic acid ( H5IO6). The reaction mixture was stirred at 80 °C for 2 h under nitrogen protection. After completion of the reaction, the reaction mixture was extracted three times with ether (50 mL). The organic layers were combined and dried with anhydrous magnesium sulfate, followed by evaporation under reduced pressure to remove the solvent. The resulting crude product was purified by silica gel column chromatography to afford 3.23 g of intermediate compound B (3-iodo-9phenylcarbazole) as a white solid in 87% yield.1H NMR (CDCl3, 300 MHz) δ (ppm): 8.43 (d, 1H), 8.05 (d, 1H), 7.62 (dd, 1H), 7.61-7.75 (m, 2H) , 7.51-7.43 (m, 3H), 7.41-7.35 (m, 2H), 7.27 (dd, 1H), 7.14 (d, 1H).

References[1] Patent: EP1661888, 2006, A1. Location in patent: Page/Page column 11
[2] Patent: US2008/174237, 2008, A1. Location in patent: Page/Page column 13-14
[3] Patent: EP2149555, 2010, A1. Location in patent: Page/Page column 19
[4] Patent: KR101791161, 2017, B1. Location in patent: Paragraph 0116; 0123-0128
[5] Patent: EP2738166, 2014, A1. Location in patent: Paragraph 0162

3-Iodo-N-phenylcarbazole Preparation Products And Raw materials

Raw materialsN-PHENYLCARBAZOLE HYDROCHLORIDE-->Acetic acid-->Periodic acid-->iodine
Preparation ProductsN-(4-(phenyl-9H-carbazol-3-yl)phenyl)biphenyl-4-aMine
3-Iodo-9H-carbazole CAS 16807-13-9
3-IODOPROPYLTRIMETHOXYSILANE CAS 14867-28-8
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