19264-71-2

Basic information

• Product Name: 9H-Carbazole, 9-(4-chlorophenyl)-
• CAS NO: 19264-71-2
• Molecular Formula: C18H12ClN
• Molecular Weight: 277.753
• Mol File: 19264-71-2.mol
• Article Data: 27

Chemical Properties

• CAS DataBase Reference: 9H-Carbazole, 9-(4-chlorophenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 9H-Carbazole, 9-(4-chlorophenyl)-(19264-71-2)
• EPA Substance Registry System: 9H-Carbazole, 9-(4-chlorophenyl)-(19264-71-2)

Safety Data

• Hazardous Substances Data: 19264-71-2(Hazardous Substances Data)

Upstream product

• 637-87-6 1-Chloro-4-iodobenzene 
• 86-74-8 9H-carbazole 
• 13029-09-9 2,2'-dibromobiphenyl 
• 106-47-8 4-chloro-aniline 
• 98-80-6 phenylboronic acid 
• 609-73-4 o-nitroiodobenzene 
• 86-00-0 2-nitrobiphenyl 
• 388-82-9 2,2'-difluorobiphenyl 
• 2113-51-1 2-iodobiphenyl 
• 2052-07-5 2-Bromobiphenyl 
• 3296-05-7 1-azido-4-chlorobenzene 
• 4688-76-0 2-Biphenylboronic acid 
• 615-43-0 2-iodophenylamine 
• 4316-56-7 (p-chlorophenyl)diphenylamine 

Downstream Products

• 419536-33-7 4-(carbazol-9-yl)phenylboronic acid 
• 912573-25-2 3,6-bis(trimethylsilylethynyl)-9-(p-chlorophenyl)carbazole 
• 912573-23-0 9-(p-chlorophenyl)-3,6-diethynylcarbazole 
• 912573-26-3 3,6-dibromo-9-(4-chlorophenyl)-9H-carbazole 

Relevant articles and documents

Method for synthesizing carbazole derivative

The invention aims to provide a method for synthesizing a carbazole derivative. The method is characterized in that palladium chloride is used as a catalyst, 2, 2' - dibromobiphenyl is used as an electrophilic reagent, primary amine is taken as a nucleophile, and the carbazole derivative is directly cross-coupled under the conditions of toluene as a solvent and an air atmosphere. The method has the advantages of high yield, high selectivity, simplicity and convenience in operation and the like.

Transition-metal free synthesis of: N -aryl carbazoles and their extended analogs

Herein, we describe a facile synthesis of N-arylated carbazoles via ladderization of fluorinated oligophenylenes. The reaction consists of two subsequent nucleophilic substitutions triggered by an electronic transfer from dimsyl anions. The reaction allows the effective one-pot formation of at least six C-N bonds with pronounced selectivity to the C-F bond placement.

COMPOUND FOR ORGANIC OPTOELECTRONIC DEVICE, COMPOSITION FOR ORGANIC OPTOELECTRONIC DEVICE, ORGANIC OPTOELECTRONIC DEVICE, AND DISPLAY DEVICE

The present invention relates to a compound for an organic optoelectronic device, represented by Chemical Formula 1; a composition for an organic optoelectronic device, including same; an organic optoelectronic device; and a display device. The description of Chemical Formula 1 is the same as that defined in the specification.