55542-85-3

Basic information

• Product Name: 6-phenyl-2,3,4,9-tetrahydro-1H-carbazole
• Synonyms: 6-phenyl-2,3,4,9-tetrahydro-1H-carbazole
• CAS NO: 55542-85-3
• Molecular Weight: 247.34
• Mol File: 55542-85-3.mol

Chemical Properties

• CAS DataBase Reference: 6-phenyl-2,3,4,9-tetrahydro-1H-carbazole(CAS DataBase Reference)
• NIST Chemistry Reference: 6-phenyl-2,3,4,9-tetrahydro-1H-carbazole(55542-85-3)
• EPA Substance Registry System: 6-phenyl-2,3,4,9-tetrahydro-1H-carbazole(55542-85-3)

Safety Data

• Hazardous Substances Data: 55542-85-3(Hazardous Substances Data)

Upstream product

• 5425-58-1 2-biphenyl-4-ylamino-cyclohexanone 
• 92-67-1 4-phenylalanine 
• 108-94-1 cyclohexanone 
• 92-66-0 4-bromo-1,1'-biphenyl 
• 2051-62-9 4'-biphenyl chloride 

Downstream Products

• 103012-26-6 3-phenyl-9H-carbazole 

Relevant articles and documents

One-Pot Synthesis of Indoles and Pyrazoles via Pd-Catalyzed Couplings/Cyclizations Enabled by Aqueous Micellar Catalysis

An effective one-pot synthesis of either indoles or pyrazoles can be achieved via Pd-catalyzed aminations followed by subsequent cyclizations facilitated by aqueous micellar catalysis. This new technology includes efficient couplings with low loadings of palladium, a more stable source of the required hydrazine moiety, greater atom economy for the initial coupling, and reduced reaction temperatures, all leading to environmentally responsible processes.

Mild and rapid Pd-catalyzed cross-coupling with hydrazine in continuous flow: Application to the synthesis of functionalized heterocycles

Minimizing risk: The synthesis of arylhydrazines through C?￡?N cross-coupling of aryl chlorides with hydrazine is described. Through the use of continuous flow, the hazards associated with the use of hydrazine in the presence of transition metals are decreased. In addition, multistep flow sequences have also been developed for the generation of functionalized heterocycles utilizing the arylhydrazine intermediates.

Metal-catalyzed arylations of hydrazines, hydrazones, and related substrates

A method is provided for the transition metal-catalyzed arylation, or vinylation, of hydrazines, hydrazones, and the like. Additionally, the invention provides a conceptually novel strategy, the cornerstone of which is the transition metal-catalyzed aryla

A palladium-catalyzed method for the preparation of indoles via the Fischer indole synthesis

A Pd-catalyzed method for the preparation of N-aryl benzophenone hydrazones 4 is described. The use of a Pd/BINAP-based catalyst provides hydrazones 4 in good yields. Using 0.1 mol % of a Pd/9,9-dimethyl-4,5- bis(diphenylphosphino)xanthene (Xantphos) cata