61231-45-6

Basic information

• Product Name: NAPHTHALEN-1-YL-DIPHENYL-AMINE
• Synonyms: NAPHTHALEN-1-YL-DIPHENYL-AMINE
• CAS NO: 61231-45-6
• Molecular Formula: C₂₂H₁₇N
• Molecular Weight: 295.37708
• Mol File: 61231-45-6.mol
• Article Data: 26

Chemical Properties

• Melting Point: 142°C
• Boiling Point: 427.06°C (rough estimate)
• Appearance: /
• Density: 1.0541 (rough estimate)
• Refractive Index: 1.8500 (estimate)
• CAS DataBase Reference: NAPHTHALEN-1-YL-DIPHENYL-AMINE(CAS DataBase Reference)
• NIST Chemistry Reference: NAPHTHALEN-1-YL-DIPHENYL-AMINE(61231-45-6)
• EPA Substance Registry System: NAPHTHALEN-1-YL-DIPHENYL-AMINE(61231-45-6)

Safety Data

• Hazardous Substances Data: 61231-45-6(Hazardous Substances Data)

Upstream product

• 90-11-9 1-Bromonaphthalene 
• 122-39-4 diphenylamine 
• 90-30-2 N-phenyl-1-naphthylamine 
• 637-88-7 1,4-Cyclohexanedione 
• 100-47-0 benzonitrile 
• 62-53-3 aniline 
• 86-53-3 1-Cyanonaphthalene 
• 90-14-2 1-Iodonaphthalene 
• 1144-13-4 naphthalen-1-yl N,N-dimethylsulfamate 
• 5856-90-6 sodium diphenylamine 
• 108-86-1 bromobenzene 
• 134-32-7 1-amino-naphthalene 
• 17425-91-1 N-(trimethylsilyl)-diphenylamine 
• 108-90-7 chlorobenzene 

Downstream Products

• 123847-85-8 4,4'-bis[N-(1-naphthyl)-N-phenylamino] biphenyl 

Relevant articles and documents

Iron-catalyzed synthesis, structure, and photophysical properties of tetraarylnaphthidines

We describe the synthesis and photophysical properties of tetraarylnaphthidines. Our synthetic approach is based on an iron-catalyzed oxidative C–C coupling reaction as the key step using a hexadecafluorinated iron–phthalocyanine complex as a catalyst and

DIARYL AMINE COMPOUND AND METHOD FOR PRODUCING THE SAME

The present invention relates to a process for the preparation of diaryl amine compounds. A compound represented by chemical formula 1, a compound represented by chemical formula 2, and a synthetic reagent in a solvent, the synthetic reagent being CsF, KF, 18 - crown -6, K. 2 CO3, [TBAT] The present invention relates to a process for the preparation of diaryl amine compounds comprising a material selected from the group consisting of a (tetrabutylammonium difluorotriphenylsilicate), TBAF (tetrabutylammonium fluoride) and combinations thereof. Chemical Formula 1. Chemical Formula 2. The diaryl amine compound can be synthesized under the absence of a transition metal to be used to synthesize diaryl amine compounds having various substituents.

Sonogashira-Hagihara and Buchwald-Hartwig cross-coupling reactions with sydnone and sydnone imine derived catalysts

Seven different palladium complexes of sydnones and sydnone imines and a co-catalyst system consisting of lithium sydnone-4-carboxylate and Pd(PPh3)4 catalyzed Sonogashira-Hagihara reactions between (hetero)- aromatic bromides and 2-methylbut-3-yn-2-ol (52 examples, up to 100% yield). The co-catalyst system and a sydnone Pd complex were also tested in Buchwald-Hartwig reactions (9 examples, up to 100% yield). (Equation Presented).