23866-67-3

Basic information

• Product Name: 9H-Carbazole, 9-(2-pyridinyl)-
• Synonyms: 9-(2-pyridyl)-9H-carbazole;9-[2]Pyridyl-carbazol;9-(pyridin-2-yl)-9H-carbazole;2-(N-carbazolyl)pyridine;9H-Carbazole,9-(2-pyridinyl);9-(2-pyridyl)carbazole
• CAS NO: 23866-67-3
• Molecular Formula: C17H12N2
• Molecular Weight: 244.29100
• Mol File: 23866-67-3.mol
• Article Data: 31

Chemical Properties

• CAS DataBase Reference: 9H-Carbazole, 9-(2-pyridinyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 9H-Carbazole, 9-(2-pyridinyl)-(23866-67-3)
• EPA Substance Registry System: 9H-Carbazole, 9-(2-pyridinyl)-(23866-67-3)

Safety Data

• Hazardous Substances Data: 23866-67-3(Hazardous Substances Data)

Upstream product

• 109-04-6 2-bromo-pyridine 
• 86-74-8 9H-carbazole 
• 372-48-5 2-fluoropyridine 
• 33650-06-5 sodium salt of carbazole 
• 5029-67-4 2-iodopyridine 
• 1243273-04-2 N-(2-deuteriophenyl)-2-aminopyridine 
• 1256380-82-1 (N-([1,1′-biphenyl]-2-yl)pyridin-2-amine) 
• 6631-37-4 2-(phenylamino)pyridine 
• 98-80-6 phenylboronic acid 
• 62-53-3 aniline 
• 615-36-1 2-bromoaniline 
• 239137-40-7 N-(2-bromophenyl)pyridin-2-amine 
• 3240-34-4 [bis(acetoxy)iodo]benzene 
• 504-29-0 2-aminopyridine 

Downstream Products

• 1416353-37-1 1-phenyl-9-(pyridin-2-yl)-9H-carbazole 
• 1416353-52-0 1-(p-tolyl)-9-(pyridin-2-yl)-9H-carbazole 
• 1416353-54-2 1-(4-methoxyphenyl)-9-(pyridin-2-yl)-9H-carbazole 

Relevant articles and documents

Study on Palladium(II)-Catalyzed Mono-1-alkenylation of 9 H -Carbazoles

A general and efficient method is reported for the direct mono-1-alkenylation of 9 H -carbazole molecules with divalent palladium as a catalyst and an N -(2-pyridyl)sulfanyl directing group. This method also provides an efficient synthetic route for the s

Color tuning based on a six-membered chelated iridium(III) complex with aza-aromatic ligand

A six-membered chelated iridium complex containing aza-aromatic ligand is prepared. Emission color tuning from yellow to deep red is observed for electroluminescent devices with different doping concentrations. Copyright

Palladium-Catalyzed Pyridine-Directed Regioselective Oxidative C–H Acylation of Carbazoles by Using Aldehydes as the Acyl Source

We herein report a highly regioselective reaction for the palladium-catalyzed oxidative acylation of carbazole derivatives with various aromatic and aliphatic aldehydes as the acyl source. The carbazole derivatives are N-protected with an easily removable pyridine moiety, which directs the Pd-catalyzed ortho acylation to occur at the C-1 and C-8 positions. The reactions of dibromo- and diiodo-substituted N-pyridylcarbazole derivatives, however, provide only the 1-acylated products. This method can be applied to a broad scope of substrates. A reaction mechanism has also been proposed.

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Metal complex as well as preparation method and application thereof

The invention provides a metal complex with a structure represented by a formula (I). The novel [NOON] tetradentate fourth subgroup metal complex provided by the invention is good in thermal stabilityand high in catalytic activity, is used as a main catal