92795-23-8

Basic information

• Product Name: 3-phenyl-2-nitronapthalene
• Synonyms: 3-phenyl-2-nitronapthalene
• CAS NO: 92795-23-8
• Molecular Weight: 249.269
• Mol File: 92795-23-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 3-phenyl-2-nitronapthalene(CAS DataBase Reference)
• NIST Chemistry Reference: 3-phenyl-2-nitronapthalene(92795-23-8)
• EPA Substance Registry System: 3-phenyl-2-nitronapthalene(92795-23-8)

Safety Data

• Hazardous Substances Data: 92795-23-8(Hazardous Substances Data)

Upstream product

• 71-43-2 benzene 
• 67116-33-0 2-bromo-3-nitronaphthalene 
• 98-80-6 phenylboronic acid 
• 1450995-35-3 C₁₆H₁₃NO₂ 
• 13115-28-1 3-nitronaphthalen-2-amine 

Downstream Products

• 875822-75-6 2-amino-3-phenyl-naphthalene 
• 30889-48-6 3‐phenylnaphthalen‐2‐ol 
• 1229013-43-7 (+/-)-3,3'-diphenyl-1,1'-binaphthyl-2,2'-diamine 
• 243-28-7 2,3-benzocarbazole 

Relevant articles and documents

Novel organic compounds for organic light-emitting diode and organic light-emitting diode including the same

The present invention relates to an organic electroluminescent compound represented by chemical formula A and an organic light emitting device comprising the same. Substituents A_1 to A_4, R_1 to R_18, L_1, L_2, X, Y, m, n, s, p, and q are the same as defined in the detailed description of the invention.

Regiospecific synthesis of novel cyclic nitrostyrenes and 3-substituted 2-nitronaphthalenes

A two-step, practical, regiospecific, and readily scalable benzannulation protocol for the preparation of novel 3-alkyl- and 3-aryl-substituted 2-nitronaphthalenes is disclosed. Addition of a β-nitrostyrene or nitroalkene to a solution of freshly prepared lithiated o-tolualdehyde tert-butyl imine first leads to the formation of a nitronate, via rapid 1,4-addition, then an intramolecular aza-Henry reaction takes place to afford a six-membered carbocycle. Subsequent treatment of the reaction mixture with aqueous acid affords novel substituted cyclic nitrostyrenes that can be conveniently aromatized via a one-pot radical-induced bromination and elimination sequence to furnish the corresponding 3-alkyl- or 3-aryl-2-nitronaphthalenes in excellent yields. The straightforward syntheses of 2-aminonaphthalenes, substituted BINAMs, 2-naphthols as well as tricyclic fused 1,2,3-triazoles are also described. Georg Thieme Verlag Stuttgart. New York.