3-BroMo-9-(4-broMophenyl)carbazole

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CAS:1226860-66-7
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3-BroMo-9-(4-broMophenyl)carbazole manufacturers

3-BroMo-9-(4-broMophenyl)carbazole Basic information
Product Name:3-BroMo-9-(4-broMophenyl)carbazole
Synonyms:3-BroMo-9-(4-broMophenyl)carbazole;3-Bromo-9-(4-bromophenyl)-9H-carbazole;3-Bromo-9-(4-bromophenyl)-9H-carbazole;9H-Carbazole, 3-bromo-9-(4-bromophenyl)-
CAS:1226860-66-7
MF:C18H11Br2N
MW:401.09
EINECS:
Product Categories:
Mol File:1226860-66-7.mol
3-BroMo-9-(4-broMophenyl)carbazole Structure
3-BroMo-9-(4-broMophenyl)carbazole Chemical Properties
Melting point 148.0 to 152.0 °C
Boiling point 496.4±41.0 °C(Predicted)
density 1+-.0.1 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
form powder to crystal
color White to Almost white
Safety Information
HS Code 2933.99.9701
MSDS Information
3-BroMo-9-(4-broMophenyl)carbazole Usage And Synthesis
Synthesis
(9-(4-BROMOPHENYL))-9H-CARBAZOLE

57102-42-8

3-BroMo-9-(4-broMophenyl)carbazole

1226860-66-7

General procedure for the synthesis of 3-bromo-9-(4-bromophenyl)-9H-carbazole from 9-(4-bromophenyl)carbazole: 9-(4-bromophenyl)-9H-carbazole (3.00 g, 9.31 mmol) was dissolved in dichloromethane (50 mL) under the condition of light avoidance, followed by addition of N-bromosuccinimide (NBS, 1.80 g, 10 mmol). The reaction mixture was stirred at room temperature for 12 hours. Upon completion of the reaction, water was added to the mixture and a white precipitate was precipitated. After filtration and drying, the resulting white solid was purified by recrystallization from petroleum ether. Yield: 100%.

References[1] Organic Electronics: physics, materials, applications, 2014, vol. 15, # 11, p. 2667 - 2676
[2] Patent: WO2016/28902, 2016, A1. Location in patent: Page/Page column 27, 28
[3] Patent: TW2016/25529, 2016, A. Location in patent: Paragraph 0051
[4] Advanced Materials, 2010, vol. 22, # 16, p. 1872 - 1876
3-BroMo-9-(4-broMophenyl)carbazole Preparation Products And Raw materials
Raw materials(9-(4-BROMOPHENYL))-9H-CARBAZOLE-->3-Bromo-9H-carbazole-->Carbazole-->1-Bromo-4-iodobenzene-->4-Bromofluorobenzene-->1,4-Dibromobenzene
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