62453-34-3

Basic information

• Product Name: N-(4-chlorophenyl)-9H-fluoren-9-amine
• Synonyms: N-(4-chlorophenyl)-9H-fluoren-9-amine
• CAS NO: 62453-34-3
• Molecular Weight: 291.78
• Mol File: 62453-34-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: N-(4-chlorophenyl)-9H-fluoren-9-amine(CAS DataBase Reference)
• NIST Chemistry Reference: N-(4-chlorophenyl)-9H-fluoren-9-amine(62453-34-3)
• EPA Substance Registry System: N-(4-chlorophenyl)-9H-fluoren-9-amine(62453-34-3)

Safety Data

• Hazardous Substances Data: 62453-34-3(Hazardous Substances Data)

Upstream product

• 106-47-8 4-chloro-aniline 
• 75295-62-4 2′-bromo-[1,1′-biphenyl]-2-carbaldehyde 
• 486-25-9 9-fluorenone 
• 5455-00-5 N-(9H-fluoren-9-ylidene)-4-chlorobenzenamine 

Downstream Products

• 102467-47-0 N-(4-chloro-phenyl)-N-fluoren-9-yl-acetamide 

Relevant articles and documents

Intramolecular Addition of Aryl Radicals to Carbon-Nitrogen Double Bonds

Cyclisation of radicals 6a,b is highly regioselective towards a 5-exo process; 6-endo ring closure is a minor route and their ratio depends on the substituents.No ring expansion of the five-membered radical intermediates 7a,b was observed.Radicals 27a,b give rise to 5-exo cyclisation regiospecifically.A competitive 1,5-hydrogen shift leading to imidoyl radicals was noticed.An analogous behaviour is also exhibited by vinyl radicals when allowed to add to carbon-nitrogen double bonds.

Energetics of Multistep versus One-step Hydride Transfer Reactions of Reduced Nicotinamide Adenine Dinucleotide (NADH) Models with Organic Cations and p-Quinones

Free energy changes of each elementary step involved in the formal hydride transfer (HT-) reactions (including the so-called "one-step" HT- and "multistep" HT- mechanisms) of the reduced ni