57103-13-6

Basic information

• Product Name: 9-(4-(tert-butyl)phenyl)-9H-carbazole
• Synonyms: 9-(4-(tert-butyl)phenyl)-9H-carbazole
• CAS NO: 57103-13-6
• Molecular Formula: C₂₂H₂₁N
• Molecular Weight: 299.40884
• Mol File: 57103-13-6.mol
• Article Data: 18

Chemical Properties

• Melting Point: 189.0 to 193.0 °C
• Appearance: /
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 9-(4-(tert-butyl)phenyl)-9H-carbazole(CAS DataBase Reference)
• NIST Chemistry Reference: 9-(4-(tert-butyl)phenyl)-9H-carbazole(57103-13-6)
• EPA Substance Registry System: 9-(4-(tert-butyl)phenyl)-9H-carbazole(57103-13-6)

Safety Data

• Hazardous Substances Data: 57103-13-6(Hazardous Substances Data)

Usage

Description

9-(4-(tert-butyl)phenyl)-9H-carbazole is a chemical compound with the molecular formula C28H25N. It belongs to the carbazole family and consists of a carbazole core substituted with a 4-(tert-butyl)phenyl group. 9-(4-(tert-butyl)phenyl)-9H-carbazole is known for its high thermal stability and good charge-transport properties, making it a promising candidate for various optoelectronic applications.

Uses

Used in Organic Electronics:
9-(4-(tert-butyl)phenyl)-9H-carbazole is used as a semiconductor material for its application in light-emitting devices and photovoltaic cells. Its high thermal stability and good charge-transport properties make it a promising candidate for these optoelectronic applications.
Used in Advanced Materials:
9-(4-(tert-butyl)phenyl)-9H-carbazole is also studied for its potential use in organic semiconductors, polymer blends, and other advanced materials. Its unique properties contribute to the development of innovative materials for various applications in the field of materials science.

Upstream product

• 13029-09-9 2,2'-dibromobiphenyl 
• 769-92-6 4-tert-Butylaniline 
• 7598-28-9 4-tert-butylphenyltosylate 
• 86-74-8 9H-carbazole 
• 615-43-0 2-iodophenylamine 
• 98-54-4 para-tert-butylphenol 
• 1016-05-3 dibenzothiophene sulfone 
• 2113-51-1 2-iodobiphenyl 
• 90-41-5 2-phenylaniline 
• 86-00-0 2-nitrobiphenyl 
• 609-73-4 o-nitroiodobenzene 
• 98-80-6 phenylboronic acid 
• 189999-35-7 [1,1'-biphenyl]-2,2'-iodonium trifluoromethanesulfonate 
• 35779-04-5 1-tert-butyl-4-iodobenzene 

Downstream Products

• 1133057-82-5 9-(4-tert-butylphenyl)-3-bromo-9H-carbazole 
• 1384096-17-6 9-(4-tert-butylphenyl)-3-(thiophen-2-yl)-9H-carbazole 
• 1370333-08-6 4-(5-(9-(4-tert-butylphenyl)-9H-carbazol-3-yl)thiophen-2-yl)benzaldehyde 
• 1370333-03-1 (E)-3-(4-(5-(9-(4-tert-butylphenyl)-9 H-carbazol-3-yl)thiophen-2-yl)phenyl)-2-cyanoacrylic acid 
• 1394038-62-0 C₃₀H₃₇N 
• 1219497-88-7 9-(4-tert-butylphenyl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole 
• 1132642-07-9 C₆₀H₄₃Br₂N 
• 1132642-06-8 C₆₀H₄₃Br₂N 
• 871018-06-3 C₄₈H₃₇NO₂ 
• 741293-42-5 3,6-dibromo-9-(4-(tert-butyl)phenyl)-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.

Diazine isomer blue-light material

The invention reveals a diazine isomer blue-light material. The technical scheme of the invention uses a carbazole derivative as an electron donor unit and a diazine isomer as an electron acceptor unit, the photophysical properties of a luminescent materi

A General Palladium–Phosphine Complex To Explore Aryl Tosylates in the N-Arylation of Amines: Scope and Limitations

The scope and limitations of the monoselective N-arylation of various amines by using aryl and hetaryl tosylates are presented. The air-stable and easily accessible Pd(OAc)2/CM-phos {CM-phos=2-[2-(dicyclohexylphosphino)phenyl]-1-methyl-1H-indole}catalyst system was able to deal with a wide range of aryl tosylate substrates as well as amine nucleophiles, including primary and secondary cyclic/acyclic aliphatic amines and anilines. NH-Bearing heterocycles such as indole, carbazole, pyrrole, 10-phenothiazine, and 10-phenoxazine were shown to be feasible coupling partners under this catalytic system. The described reaction conditions tolerate a wide range of functional groups and allow an array of aromatic amines as well as unsymmetrical amine products to be easily accessed from the various phenolic derivatives. Interestingly, this catalyst system even offers the opportunity to perform the reaction in water medium. We also report the intermolecular coupling of optically active α-central chiral amines with aryl tosylates without erosion of the enantiomeric purity.