57103-20-5

Basic information

• Product Name: 3,6-DIBROMO-9-PHENYLCARBAZOLE
• Synonyms: 3,6-DIBROMO-9-PHENYLCARBAZOLE;3,6-DibroMo-9-phenylarbazole;3,6-DibroMo-9-phenylarbazole,98%;3,6-DibroMo-9-phenylcarbazole,,6-DIBROMO-9-PHENYLCARBAZOLE;9H-Carbazole, 3,6-dibroMo-9-phenyl- 3,6-DibroMo-9-phenyl-9H-carbazole;6-dibroMo -9-phenylcarbazole
• CAS NO: 57103-20-5
• Molecular Formula: C₁₈H₁₁Br₂N
• Molecular Weight: 401.09
• EINECS: 1312995-182-4
• Product Categories: Carbazoles;Carbazoles (for Conduting Polymer Research);Functional Materials;Reagents for Conducting Polymer Research;carbazole;OLED materials,pharm chemical,electronic;OLED intermediate
• Mol File: 57103-20-5.mol
• Article Data: 35

Chemical Properties

• Melting Point: 160-164℃
• Boiling Point: 505.261 °C at 760 mmHg
• Flash Point: 259.373 °C
• Appearance: /
• Density: 1.642 g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.7
• Storage Temp.: Inert atmosphere,Room Temperature
• Solubility: soluble in dichloromethane
• CAS DataBase Reference: 3,6-DIBROMO-9-PHENYLCARBAZOLE(CAS DataBase Reference)
• NIST Chemistry Reference: 3,6-DIBROMO-9-PHENYLCARBAZOLE(57103-20-5)
• EPA Substance Registry System: 3,6-DIBROMO-9-PHENYLCARBAZOLE(57103-20-5)

Safety Data

• Hazard Codes: Xn
• Statements: 22-41
• Safety Statements: 26-39-24/25
• WGK Germany: 3
• Hazardous Substances Data: 57103-20-5(Hazardous Substances Data)

Usage

Chemical Properties

off-white powder

InChI:InChI=1/C18H11Br2N/c19-12-6-8-17-15(10-12)16-11-13(20)7-9-18(16)21(17)14-4-2-1-3-5-14/h1-11H

Upstream product

• 57102-42-8 N-(4-bromophenyl)carbazole 
• 462-06-6 fluorobenzene 
• 108-86-1 bromobenzene 
• 6825-20-3 3,6-dibromo-9H-carbazole 
• 591-50-4 iodobenzene 
• 4043-87-2 pipecolic Acid 
• 86-74-8 9H-carbazole 
• 1150-62-5 N-phenylcarbazole 

Downstream Products

• 618442-57-2 9-phenyl-3,6-bis-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole 
• 1097245-00-5 3-bromo-9-phenyl-6-(triphenylsilyl)-9-carbazole 
• 145771-93-3 9-phenyl-9H-carbazole-3,6-dicarbaldehyde 
• 1221237-81-5 3-bromo-6-methyl-9-phenyl-9H-carbazole 
• 1221237-01-9 C₄₆H₃₆N₂ 
• 1221237-21-3 C₆₁H₄₈N₂ 
• 1221238-01-2 C₂₅H₁₈ClN 
• 854952-58-2 N-phenyl-9H-carbazol-3-boronic acid 

Relevant articles and documents

Synthesis of carbazole-based small organic molecule hole transport material and application of carbazole-based small organic molecule hole transport material in perovskite solar cell

The invention belongs to the field of perovskite solar cell materials, and discloses a carbazole-based small organic molecule hole transport material. According to the carbazole-based small organic molecule hole transport material, a carbazole intermediate core group fragment is synthesized by utilizing a low-temperature reaction and a bromination reaction; a target product OY1, a target product OY2 and a target product OY3 are obtained by means of synthesis from the carbazole intermediate core group fragment and peripheral triphenylamine micromolecules through an acylation reaction and a coupling reaction; the structures of the target product OY1, the target product OY2 and the target product OY3 are confirmed through a high-resolution mass spectrum characterization means, and the target product OY1, the target product OY2 and the target product OY3 are applied to a perovskite solar cell; the synthesized compound is subjected to photophysic, electrochemical, intrinsic hole mobility and thin film characteristic tests, and in addition, the photovoltaic performance of the perovskite solar cell is represented through tests of output current-voltage, incident monochromatic photon-electron conversion efficiency, long-term stability and the like of the cell device. Due to low cost, easy chemical synthesis and excellent performance, the carbazole-based small organic molecule hole transport material will become a powerful competitor.

Monomer compounds comprising uracil group, Organic layers comprising the cross-linked of the monomer compounds, and Organic electronic device comprising the organic layers

The present invention provides a pyrimidine-based functional group-containing monomolecular compound represented by chemical formula 1 of Ar-(R_1-R_2-Py)_n as a material for an organic layer of an organic electronic device. The compound can form an organic layer within a short time through photo-curing at room temperature. In chemical formula 1, n is 2-10; Ar is a substituted or non-substituted C_6-C_60 aryl group, or a substituted or non-substituted C_3-C_60 heteroaryl group having an n-valent linking group; each of R_1 and R_2 independently represents a single bond, -O-, a substituted or non-substituted C_6-C_30 arylene group, a substituted or non-substituted C_3-C_30 heteroarylene group, a substituted or non-substituted C_1-C_10 alkylene group, a substituted or non-substituted C_1-C10 alkoxylene group, a substituted or non-substituted amide group, or a substituted or non-substituted amine group; and Py is a monovalent linking group derived from a pyrimidine-based functional group.COPYRIGHT KIPO 2020

Symmetric fluorenylbenzimidazole derivative and preparation method therefor

The invention relates to a symmetric fluorenylbenzimidazole derivative and a preparation method therefor. The compound has a structural general formula represented by a formula shown in the description. The method is convenient, universal and economical. The compound has an extensive application prospect in the fields of organic photoelectric materials and fluorescence probing based analysis; in addition, the compound has a symmetrical structure, so that the molecular thermal stability of the compound is improved greatly, and the manufacturing of OLED (Organic Light Emitting Diode) light-emitting devices is better facilitated.