115761-64-3

Basic information

• Product Name: 1-Amino-3-phenylnaphthalene
• Synonyms: 1-Amino-3-phenylnaphthalene
• CAS NO: 115761-64-3
• Molecular Formula: C₁₆H₁₃N
• Molecular Weight: 219.28112
• Mol File: 115761-64-3.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-Amino-3-phenylnaphthalene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Amino-3-phenylnaphthalene(115761-64-3)
• EPA Substance Registry System: 1-Amino-3-phenylnaphthalene(115761-64-3)

Safety Data

• Hazardous Substances Data: 115761-64-3(Hazardous Substances Data)

Usage

Chemical classification

Polycyclic aromatic hydrocarbon (PAH)

Structural features

Contains an amino group and a phenyl group attached to a naphthalene backbone

Applications

a. Fluorescent dye
b. Potential use as an anti-cancer agent

Safety concerns

a. Mutagenic effects
b. Genotoxic effects

Hazardous properties

a. Harmful if swallowed
b. Harmful if inhaled
c. Harmful if in contact with skin

Precautions

Proper safety measures should be followed when handling and using this compound

Upstream product

• 115902-63-1 1-(hydroxyimino)-3-phenyl-1,2,3,4-tetrahydronaphthalene 
• 30069-65-9 3-phenylnaphthalen-1-ol 
• 14944-26-4 3-phenyl-1-tetralone 
• 171258-08-5 2-(phenylethynyl)acetophenone 

Relevant articles and documents

Synthesis of α-Aminonaphthalenes via Copper-Catalyzed Aminobenzannulation of (o -Alkynyl)arylketones with Amines

A copper-catalyzed aminobenzannulation of (o-alkynyl)arylketones with amines has been developed. This method features the use of a cheap copper catalyst, the facile annulation involving various amines, and the good functional group tolerance. (Chemical Equation Presented).

Silver-catalysed intramolecular cyclisation of 2-alkynylacetophenones and 3-acetyl-2-alkynylpyridines in the presence of ammonia

Silver-catalysed/microwave-assisted domino reactions of 2-alkynyl-acetophenones and 3-acetyl-2-alkynylpyridines in the presence of ammonia are widely described. In most cases the reaction give a mixture of the imino- and carbo-cyclisation products, with a

Synthesis of 3-aryl-1-naphthalenamines

1-(Hydroxyimino)-3-aryl-1,2,3,4-tetrahydronaphthalenes, when subjected to Semmler-Wolff reaction using Beckmann's mixture, give hitherto unknown 3-aryl-1-naphthalenamines, which have been characterised using elemental analyses and spectral data.