19264-68-7

Basic information

• Product Name: 9-BENZOYLCARBAZOLE
• Synonyms: 9-BENZOYLCARBAZOLE;9-benzoyl-9h-carbazol;9-benzoyl-carbazol;(9H-carbazol-9-yl)(phenyl)Methanone;carbazol-9-yl(phenyl)methanone
• CAS NO: 19264-68-7
• Molecular Formula: C₁₉H₁₃NO
• Molecular Weight: 271.31
• EINECS: 243-031-7
• Product Categories: Carbazoles;Carbazoles (for Conduting Polymer Research);Functional Materials;Reagents for Conducting Polymer Research
• Mol File: 19264-68-7.mol
• Article Data: 29

Chemical Properties

• Melting Point: 101 °C
• Boiling Point: 391.2°Cat760mmHg
• Flash Point: 190.4°C
• Appearance: /
• Density: 1.16g/cm³
• Vapor Pressure: 1.14mmHg at 25°C
• Refractive Index: 1.499
• Solubility: soluble in Toluene
• CAS DataBase Reference: 9-BENZOYLCARBAZOLE(CAS DataBase Reference)
• NIST Chemistry Reference: 9-BENZOYLCARBAZOLE(19264-68-7)
• EPA Substance Registry System: 9-BENZOYLCARBAZOLE(19264-68-7)

Safety Data

• RTECS: FE5780000
• Hazardous Substances Data: 19264-68-7(Hazardous Substances Data)

Usage

General Description

9-BENZOYLCARBAZOLE is a chemical compound that belongs to the class of carbazole derivatives. It is a yellowish powder that is insoluble in water but soluble in organic solvents. 9-BENZOYLCARBAZOLE has been studied for its potential applications in organic electronic devices, such as organic light-emitting diodes (OLEDs) and organic photovoltaic cells (OPVs), due to its high thermal stability and good electron transporting properties. It has also been investigated for its potential antioxidant, anti-inflammatory, and neuroprotective activities. Furthermore, 9-BENZOYLCARBAZOLE has shown promise in the field of medicinal chemistry, as it exhibits anti-tumor and anti-cancer properties in certain studies. Overall, 9-BENZOYLCARBAZOLE is a versatile compound with a wide range of potential applications in various fields.

InChI:InChI=1/C5H10Br2/c1-4(6)3-5(2)7/h4-5H,3H2,1-2H3

Upstream product

• 86-74-8 9H-carbazole 
• 98-88-4 benzoyl chloride 
• 93-97-0 benzoic acid anhydride 
• 611-74-5 N,N-dimethylbenzamide 
• 769-78-8 vinyl benzoate 
• 82390-31-6 N-(2-biphenylyl)-N-hydroxybenzamide 
• 19402-87-0 9-benzyl-9H-carbazole 
• 125424-72-8 (9H-carbazol-9-yl)(2-iodophenyl)methanone 
• 21711-71-7 2-phenylnitrosobenzene 
• 16169-17-8 N-([1,1'-biphenyl]-2-yl)hydroxylamine 
• 7404-97-9 2-(benzoylamino)biphenyl 
• 591-50-4 iodobenzene 
• 13939-06-5 molybdenum hexacarbonyl 
• 15310-02-8 o-iodobenzanilide 

Downstream Products

• 101880-09-5 9-benzoyl-3-nitro-carbazole 
• 19264-66-5 9H-carbazole-3-yl(phenyl)methanone 
• 86-74-8 9H-carbazole 
• 65-85-0 benzoic acid 
• 78901-33-4 3,6-dibenzoylcarbazole 
• 111960-27-1 1-Benzoylcarbazole 
• 125424-75-1 9-acetyl-3-benzoylcarbazole 
• 1219637-88-3 1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole 
• 5041-48-5 3-butyl-2-phenyl-1H-inden-1-one 
• 13304-52-4 2-methyl-3-phenylinden-1-one 
• 10408-73-8 3-methyl-2-phenyl-inden-1-one 
• 1264166-21-3 2,3-bis(4-fluorophenyl)-1H-inden-1-one 
• 96286-65-6 2,3-bis(4-chlorophenyl)-1H-inden-1-one 
• 41099-25-6 2,3-bis (4-methoxyphenyl)-1H-inden-1-one 

Relevant articles and documents

Palladium-catalyzed phosphination and amination through C–H bond functionalization on biphenyl: Amido-substituent as directing group

The formation of N-(2’-(diphenylphosphoryl)-[1,1′-biphenyl]-2-yl)-2,3,4,5,6-pentafluorobenzamide (3_eaaa) has been achieved through the palladium-catalyzed and Ag(I)-assisted C–H functionalization of N-([1,1′-biphenyl]-2-yl)-2,3,4,5,6-pentafluorobenzamide

Method for the synthesis of 1-carbazole-boric acid pinacol ester by amide ortho-orthogonal directing borification

The present invention discloses a method of synthesizing 1-carbazole - boronic acid pinacol ester by orthophoreinization of an amide orthostatic directional boronate, the steps comprising: (1) the carbazole and the amidation reagent under the action of a

X-ray excited ultralong room-temperature phosphorescence for organic afterglow scintillators

We present X-ray-excitable organic ultralong room temperature phosphorescence (X-OURTP) for afterglow scintillators through implanting lone-pair electron involved n-π? transitions and efficient charge transfer characters into H-aggregations of organic cry