58328-30-6

Usage

Uses

Used in Organic Synthesis:
Indolo[3,2-b]carbazole, 5,11-dihydro-5,11-diphenylis utilized as a precursor in the synthesis of various organic compounds. Its unique structure allows for the creation of a wide range of molecules with different properties and applications, making it a valuable component in the field of organic chemistry.
Used in Pharmaceutical Research:
As a research tool, Indolo[3,2-b]carbazole, 5,11-dihydro-5,11-diphenylaids in the study of chemical reactions and biological processes. Its potential implications in pharmaceuticals include the development of new drugs and the understanding of molecular interactions within biological systems.
Used in Materials Science:
Indolo[3,2-b]carbazole, 5,11-dihydro-5,11-diphenylalso holds promise in materials science, where its properties can be harnessed to develop new materials with specific characteristics. Its use in this field can lead to advancements in areas such as electronics, optoelectronics, and nanotechnology.

Upstream product

• 945391-02-6 2',5'-bis(1,1,2,2,3,3,4,4,4-nonafluorobutanesulfonyloxy)-2,2''-dichloro[1,1':4',1''-terphenyl] 
• 62-53-3 aniline 
• 945391-01-5 2,2''-dichloro[1,1':4',1''-terphenyl]-2',5'-diol 
• 108-86-1 bromobenzene 
• 6336-32-9 5H,11H-indolo[3,2-b]carbazole 
• 121655-03-6 2,2''-dichloro-2',5'-dimethoxy[1,1':4',1''-terphenyl] 
• 3900-89-8 2-Chlorobenzeneboronic acid 
• 51560-21-5 1,4-diiodo-2,5-dimethoxybenzene 

Downstream Products

• 1338068-89-5 C₃₀H₁₉IN₂ 
• 1338068-90-8 5,11-diphenyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxoborolan-2-yl)-5,11-dihydroindolo[3,2-b]carbazole 
• 1338068-91-9 C₃₆H₂₃BrN₂ 
• 1338068-92-0 C₄₈H₃₃N₃ 
• 1246562-25-3 C₆₃H₄₅N₃ 

Relevant academic research and scientific papers

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.

Heterocyclic compound and organic light-emitting device including the same

A heterocyclic compound, an organic light-emitting device, and a flat panel display apparatus, the compound being represented by Formula 1, below:

Condensed-Cyclic Compound and Organic Light-Emitting Device Including the Same

A condensed-cyclic compound and an OLED including the same, the condensed-cyclic compound represented by Formula 1 below:

Synthesis of ladder-type π-conjugated heteroacenes via palladium-catalyzed double N-arylation and intramolecular O-arylation

(Chemical Equation Presented) Ladder-type heteroacenes containing pyrrole or furan rings, indolo[3,2-b]carbazoles and dibenzo[d,d′]-benzo[1,2-b:4,5- b′]difurans, were effectively synthesized from the common intermediates, 2,5-bis(o-chloroaryl)hydroquinones. The key reactions are palladium-catalyzed double N-arylation of aniline and intramolecular O-arylation, which enable regioselective ring closure. In addition to the parent indolo[3,2-b]carbazole and dibenzo[d,d′]benzo[1,2-b:4,5-b′]difuran, their derivatives with an alkyl or cyano group were first synthesized. Photophysical and electrochemical studies showed that the obtained heteroacenes have lower HOMO energy levels and larger band gaps than the corresponding hydrocarbon acene, pentacene. An X-ray analysis of dibenzo[d,d′]benzo[1,2-b:4,5-b′] difuran revealed that it was packed in herringbone fashion.