Production Method 1

1592-95-6

90-14-2

934545-83-2

Reaction Conditions

1.1 Reagents: Potassium carbonate Catalysts: Copper Solvents: Toluene ;  rt → 150 °C; 24 h, 150 °C

Reference

Preparation of anthracene-based compounds useful as electroluminescent material in OLED

, China, , ,

Production Method 2

1592-95-6

90-14-2

934545-83-2

Reaction Conditions

1.1 Reagents: Sodium tert-butoxide Catalysts: Triphenylphosphine ,  Tris(dibenzylideneacetone)dipalladium Solvents: Toluene ;  100 °C

Reference

Preparation of carbazole compounds as organic electronic device materials

, World Intellectual Property Organization, , ,

Production Method 3

22034-43-1

934545-83-2

Reaction Conditions

1.1 Reagents: N-Bromosuccinimide Solvents: Dichloromethane ;  12 h, rt
1.2 Reagents: Water ;  rt

Reference

Triazine-based compounds and organic light-emitting devices including triazine-based compounds

, United States, , ,

Production Method 4

1592-95-6

90-14-2

934545-83-2

Reaction Conditions

1.1 Reagents: Sodium tert-butoxide Catalysts: Triphenylphosphine ,  Tris(dibenzylideneacetone)dipalladium Solvents: Toluene ;  100 °C

Reference

Carbazole compounds as organic electronic device materials

, Korea, , ,

Production Method 5

22034-43-1

934545-83-2

Reaction Conditions

1.1 Reagents: N-Bromosuccinimide Solvents: Dichloromethane ;  rt; 24 h, rt
1.2 Reagents: Hydrochloric acid Solvents: Water ;  rt

Reference

Organic light-emitting device

, United States, , ,

Production Method 6

934545-83-2

Reaction Conditions

Reference

Preparation of carbazole compounds for electronic device

, Korea, , ,

Production Method 7

22034-43-1

934545-83-2

Reaction Conditions

1.1 Reagents: N-Bromosuccinimide Solvents: Toluene ,  Ethyl acetate ;  36 h, rt

Reference

Organic compounds, light-emitting components, light-emitting devices, electronic devices, and lighting devices

, European Patent Organization, , ,

Production Method 8

1592-95-6

90-14-2

934545-83-2

Reaction Conditions

1.1 Catalysts: Tributylphosphine ,  Tris(dibenzylideneacetone)dipalladium Solvents: Toluene ,  Water ;  12 h, rt

Reference

Organic light-emitting devices and displays with emitting layers employing multiple hosts

, United States, , ,

Production Method 9

1592-95-6

90-14-2

934545-83-2

Reaction Conditions

1.1 Reagents: Potassium carbonate Catalysts: Copper ,  18-Crown-6 Solvents: Dimethylformamide ;  24 h, 140 °C

Reference

Preparation of carbazole compounds for electronic device

, World Intellectual Property Organization, , ,

Production Method 10

22034-43-1

934545-83-2

Reaction Conditions

1.1 Reagents: N-Bromosuccinimide Catalysts: Benzoyl peroxide Solvents: Dichloromethane ;  rt

Reference

Organic electronic element containing light efficiency improving layer and electronic device containing the same

, Korea, , ,

Production Method 11

1592-95-6

90-14-2

934545-83-2

Reaction Conditions

1.1 Reagents: Potassium carbonate ,  Sodium sulfate Catalysts: Copper Solvents: Nitrobenzene ;  200 °C

Reference

Heteroaryl compounds as organic electronic device materials

, World Intellectual Property Organization, , ,

Production Method 12

1592-95-6

90-14-2

934545-83-2

Reaction Conditions

1.1 Reagents: Potassium carbonate ,  Sodium sulfate Catalysts: Copper Solvents: Nitrobenzene ;  200 °C

Reference

Carbazole compounds for organic electronic device

, Korea, , ,

Production Method 13

1592-95-6

90-14-2

934545-83-2

Reaction Conditions

1.1 Reagents: Sodium tert-butoxide Catalysts: Triphenylphosphine ,  Tris(dibenzylideneacetone)dipalladium Solvents: Toluene ;  100 °C

Reference

Preparation of heteroaromatic compound for organic electronic element and electronic device thereof

, World Intellectual Property Organization, , ,

Production Method 14

1592-95-6

90-14-2

934545-83-2

Reaction Conditions

1.1 Reagents: Potassium carbonate ,  Sodium sulfate Catalysts: Copper Solvents: Nitrobenzene ;  200 °C

Reference

Carbazole compounds as capping layer materials and electronic device thereby

, Korea, , ,

Production Method 15

934545-83-2

Reaction Conditions

Reference

Preparation of arylamine compounds for organic electroluminescent devices and display devices

, Korea, , ,

3-Bromo-9-(naphthalen-1-yl)-9H-carbazole Raw materials

• 3-Bromo-9H-carbazole
• 9-(Naphthalen-1-yl)-9H-carbazole
• 1-Iodonaphthalene

3-Bromo-9-(naphthalen-1-yl)-9H-carbazole Preparation Products

• 3-Bromo-9-(naphthalen-1-yl)-9H-carbazole (934545-83-2)

• 1. Fate of single walled carbon nanotubes in wetland ecosystems?
  Joseph H. Bisesi,Tara Sabo-Attwood Environ. Sci.: Nano, 2014,1, 574-583
• 2. Estimation of activation energy for electroporation and pore growth rate in liquid crystalline and gel phases of lipid bilayers using molecular dynamics simulations?
  Amit Kumar Majhi,Subbarao Kanchi,V. Venkataraman,K. G. Ayappa,Prabal K. Maiti Soft Matter, 2015,11, 8632-8640
• 3. Enabling chloride salts for thermal energy storage: implications of salt purity?
  J. Matthew Kurley,Phillip W. Halstenberg,Abbey McAlister,Stephen Raiman,Richard T. Mayes RSC Adv., 2019,9, 25602-25608
• 4. Emerging investigator series: kinetics of diopside reactivity for carbon mineralization in mafic–ultramafic rocks
  BrianaAguila,LandonHardee,H.ToddSchaef,SiavashZare,MohammadJavadAbdolhosseiniQomi,JarrodV.Crum,JadeE.HollimanJr.,ElenaTajueloRodriguez,LawrenceM.Anovitz,KevinM.Rosso,QuinR.S.Miller
• 5. Distinct roles of SNARE-mimicking lipopeptides during initial steps of membrane fusion?
  Alena Koukalová,?árka Pokorná,Aimee L. Boyle,Nestor Lopez Mora,Alexander Kros,Martin Hof,Radek ?achl Nanoscale, 2018,10, 19064-19073

• 73087-83-9(3,6-Dibromo-9-(4-bromophenyl)-9H-carbazole)
• 1210469-11-6(10-bromo-7-phenyl-benzo[c]carbazole)
• 934545-80-9(3-Bromo-9-(naphthalen-2-yl)-9H-carbazole)
• 1537218-76-0(3'-Bromo-1,4-di(9-carbazolyl)benzene)
• 57103-20-5(3,6-Dirbomo-9-phenylcarbazole)
• 1153-85-1(3-Bromo-9-phenylcarbazole)
• 174621-52-4(1-(4-bromophenyl)-1H-Indole)
• 185112-61-2(9-(3-Bromophenyl)carbazole)
• 57102-42-8(9-(4-Bromophenyl)-9H-carbazole)
• 750573-26-3(9-(3,5-Dibromophenyl)-9h-carbazole)