Production Method 1

34292-03-0

934545-80-9

Reaction Conditions

1.1 Reagents: N-Bromosuccinimide Solvents: Dimethylformamide ;  4 h, rt

Reference

Novel organic electroluminescent compounds having high luminous efficiency for improved driving lifespan and greater efficiency in electroluminescent devices, and organic electroluminescent devices comprising the organic electroluminescent compounds

, World Intellectual Property Organization, , ,

Production Method 2

1592-95-6

612-55-5

934545-80-9

Reaction Conditions

1.1 Reagents: Potassium carbonate Catalysts: Copper ,  18-Crown-6 Solvents: Dimethylformamide ;  24 h, 140 °C; 140 °C → rt
1.2 Reagents: Hydrochloric acid Solvents: Water ;  30 min, rt

Reference

Preparation of carbazole compounds for electronic device

, World Intellectual Property Organization, , ,

Production Method 3

1592-95-6

580-13-2

934545-80-9

Reaction Conditions

1.1 Reagents: Sodium tert-butoxide Catalysts: Tris(dibenzylideneacetone)dipalladium ,  2-Dicyclohexylphosphino-2′,6′-dimethoxybiphenyl Solvents: Toluene ;  rt → 108 °C; 3 h, 108 °C

Reference

Adamantyl-containing carbazole-type organic compounds, organic electroluminescent device and electronic device comprising the same

, China, , ,

Production Method 4

1592-95-6

612-55-5

934545-80-9

Reaction Conditions

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

Reference

Amine based hole transport layer and carbazole-based light emitting auxiliary layer for organic electroluminescent device

, Korea, , ,

Production Method 5

1592-95-6

612-55-5

934545-80-9

Reaction Conditions

1.1 Reagents: Sodium tert-butoxide Catalysts: Tri-tert-butylphosphine ,  Tris(dibenzylideneacetone)dipalladium Solvents: o-Xylene ;  16 h, 135 - 140 °C

Reference

Preparation of (dibenzofuranyl)indolo[2,3-b]carbazole derivatives as organic light emitting layer and its applications in OLEDs

, China, , ,

Production Method 6

1592-95-6

580-13-2

934545-80-9

Reaction Conditions

1.1 Reagents: Potassium carbonate Catalysts: 1,10-Phenanthroline ,  Cuprous iodide Solvents: Dimethylformamide ;  16 h, 150 °C

Reference

Organic electroluminescence device and amine compound for organic electroluminescence device

, United States, , ,

Production Method 7

1592-95-6

612-55-5

934545-80-9

Reaction Conditions

1.1 Reagents: Potassium acetate Catalysts: 1,10-Phenanthroline ,  Cuprous iodide Solvents: Dimethylformamide ;  18 h, rt → reflux

Reference

Two organic host materials for organic optoelectronic element and display device

, World Intellectual Property Organization, , ,

Production Method 8

1592-95-6

612-55-5

934545-80-9

Reaction Conditions

1.1 Reagents: Potassium carbonate Catalysts: 1,10-Phenanthroline ,  Cuprous iodide Solvents: Xylene ;  6 h, reflux

Reference

Preparation of phosphindolo[2,3-b]carbazole 7-oxide derivatives for organic electroluminescent devices

, Korea, , ,

Production Method 9

1592-95-6

612-55-5

934545-80-9

Reaction Conditions

1.1 Reagents: Sodium tert-butoxide Catalysts: Copper ,  18-Crown-6 Solvents: Toluene ;  24 h, 100 °C

Reference

Azacarbazole compounds as organic electronic device materials

, World Intellectual Property Organization, , ,

Production Method 10

1592-95-6

612-55-5

934545-80-9

Reaction Conditions

1.1 Reagents: Potassium carbonate Catalysts: 1,10-Phenanthroline ,  Cuprous iodide ,  18-Crown-6 Solvents: Dimethylformamide ;  overnight, rt → reflux

Reference

Preparation of heterocyclic compounds for organic electroluminescent devices

, China, , ,

Production Method 11

1592-95-6

612-55-5

934545-80-9

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 12

34292-03-0

934545-80-9

Reaction Conditions

1.1 Reagents: N-Bromosuccinimide Solvents: Tetrahydrofuran ;  20 h, rt

Reference

Hole transport materials and organic electroluminescent devices using them

, Korea, , ,

Production Method 13

34292-03-0

934545-80-9

Reaction Conditions

1.1 Reagents: N-Bromosuccinimide Catalysts: Benzoyl peroxide Solvents: Dichloromethane ;  12 h, rt

Reference

New bipolar green host materials containing benzimidazole-carbazole moiety in phosphorescent OLEDs

Park, Jung Hwan; Kim, Eun Kyung; El-Deeb, Ibrahim M.; Jung, Su Jin; Choi, Dae Hyuk; et al, Bulletin of the Korean Chemical Society, 2011, 32(3), 841-846

Production Method 14

580-13-2

934545-80-9

Reaction Conditions

1.1 Reagents: Potassium carbonate ,  Cuprous iodide Catalysts: 18-Crown-6 Solvents: 1,3-Dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone ;  5 h, reflux; reflux → rt
1.2 Reagents: Water ;  rt; 30 min, rt
1.3 Reagents: N-Bromosuccinimide Solvents: Dimethylformamide ;  40 min, 0 °C; overnight, rt
1.4 Reagents: Water

Reference

preparation of 1,2-benzo[a]anthracene derivatives as organic electroluminescent materials

, China, , ,

Production Method 15

1592-95-6

612-55-5

934545-80-9

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 16

1592-95-6

612-55-5

934545-80-9

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 17

1592-95-6

612-55-5

934545-80-9

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 18

1592-95-6

612-55-5

934545-80-9

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, , ,

3-Bromo-9-(naphthalen-2-yl)-9H-carbazole Raw materials

• 3-Bromo-9H-carbazole
• 9-(naphthalen-2-yl)-9H-carbazole
• 2-Iodonaphthalene
• 2-Bromonaphthalene

3-Bromo-9-(naphthalen-2-yl)-9H-carbazole Preparation Products

• 3-Bromo-9-(naphthalen-2-yl)-9H-carbazole (934545-80-9)

• 1. An amorphous lanthanum–iridium solid solution with an open structure for efficient water splitting?
  Wei Sun,Chenglong Ma,Xinlong Tian,Jianjun Liao,Ji Yang,Chengjun Ge,Weiwei Huang J. Mater. Chem. A, 2020,8, 12518-12525
• 2. An automatic determination of thoria in thoria-urania mixtures
  Analyst, 1966,91, 208-210
• 3. An aptasensor for detection of potassium ions based on RecJf exonuclease mediated signal amplification
  Bidou Wang,Xifeng Chen Analyst, 2014,139, 5695-5699
• 4. An anti-ultrasonic-stripping effect in confined micro/nanoscale cavities and its applications for efficient multiscale metallic patterning?
  Quan Xiang,Yiqin Chen,Zhiqin Li,Kaixi Bi,Guanhua Zhang,Huigao Duan Nanoscale, 2016,8, 19541-19550
• 5. An approach to the structure and vibrational analysis of cis- and trans-3-chlorostyrene through IR/Raman and INS spectroscopies and theoretical ab initio/DFT calculations?
  J. M. Granadino-Roldán,M. Fernández-Gómez,A. Navarro,T. Pe?a Ruiz,U. A. Jayasooriya Phys. Chem. Chem. Phys., 2004,6, 1133-1143

• Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Indoles and derivatives Carbazoles
• Solvents and Organic Chemicals Organic Compounds Organic Halides

• 73087-83-9(3,6-Dibromo-9-(4-bromophenyl)-9H-carbazole)
• 1210469-11-6(10-bromo-7-phenyl-benzo[c]carbazole)
• 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)
• 911660-69-0(Benzenamine, 3-(5-bromo-1H-indol-1-yl)-)
• 94994-62-4(2-Bromo-9-phenyl-9H-carbazole)
• 934545-83-2(3-Bromo-9-(naphthalen-1-yl)-9H-carbazole)