87833-80-5

Basic information

• Product Name: 1-Amino-4-phenylnaphthalene
• Synonyms: 1-Amino-4-phenylnaphthalene
• CAS NO: 87833-80-5
• Molecular Formula: C₁₆H₁₃N
• Molecular Weight: 219.28112
• Mol File: 87833-80-5.mol
• Article Data: 6

Chemical Properties

• Melting Point: 73-74 °C
• Boiling Point: 140-146 °C(Press: 14 Torr)
• Appearance: /
• Density: 1.147±0.06 g/cm3(Predicted)
• PKA: 3.99±0.10(Predicted)
• CAS DataBase Reference: 1-Amino-4-phenylnaphthalene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Amino-4-phenylnaphthalene(87833-80-5)
• EPA Substance Registry System: 1-Amino-4-phenylnaphthalene(87833-80-5)

Safety Data

• Hazardous Substances Data: 87833-80-5(Hazardous Substances Data)

Usage

General Description

1-Amino-4-phenylnaphthalene, also known as 4-phenyl-1-naphthylamine, is a chemical compound that belongs to the family of aromatic amines. It is a yellow crystalline solid with a molecular formula of C16H13N. 1-Amino-4-phenylnaphthalene is primarily used as a precursor for the production of dyes, particularly those used in the textile industry. It has also been found to have potential applications in the field of organic synthesis and chemical research. However, 1-Amino-4-phenylnaphthalene has been associated with health hazards, as it is classified as a possible carcinogen and is known to cause skin and eye irritation. Therefore, proper safety precautions should be taken when handling and using this chemical.

Upstream product

• 33457-01-1 1-nitro-4-phenyl-naphthalene 
• 6921-40-0 1-azidonaphthalene 
• 71-43-2 benzene 
• 86-57-7 1-Nitronaphthalene 
• 2298-07-9 4-Bromo-1-naphthylamine 
• 98-80-6 phenylboronic acid 
• 605-02-7 1-phenylnaphthalene 
• 7469-40-1 1-phenyl-3,4-dihydronaphthalene 
• 529-34-0 3,4-dihydronaphthalene-1(2H)-one 

Downstream Products

• 109590-62-7 5-phenyl-1H-benz[g]indole-2,3-dione 
• 36159-76-9 4-phenyl-1-naphthol 
• 856212-75-4 4-phenyl-naphthalene-1,2-diyldiamine 
• 949462-19-5 N-(biphenyl-4-yl)-4-phenylnaphthalen-1-amine 
• 1407504-41-9 C₁₉H₁₁Cl₂N 
• 1407504-42-0 C₂₅H₁₆ClN 
• 1407502-89-9 C₄₄H₂₉N₃ 
• 1407502-90-2 C₄₄H₂₉N₃ 
• 956285-35-1 4-phenylnaphthalene-1-sulfonic acid dimethylamide 

Relevant articles and documents

Aurora Kinase Modulators and Method of Use

The present invention relates to chemical compounds having a general formula I wherein A1-8, D′, L1, L2, R1, R6-8 and n are defined herein, and synthetic intermediates, which are capable of modulating various protein kinase receptor enzymes and, thereby, influencing various disease states and conditions related to the activities of such kinases. For example, the compounds are capable of modulating Aurora kinase thereby influencing the process of cell cycle and cell proliferation to treat cancer and cancer-related diseases. The invention also includes pharmaceutical compositions, including the compounds, and methods of treating disease states related to the activity of Aurora kinase.

AROMATIC AMINE DERIVATIVE AND ORGANIC ELECTROLUMINESCENT DEVICE USING SAME

Provided are a novel aromatic amine derivative represented by the following general formula (1) and an organic electroluminescent device including an organic thin film formed of one or a plurality of layers including at least a light emitting layer interposed between a cathode and an anode, in which at least one layer of the organic thin film contains the aromatic amine derivative alone or as a component of a mixture, which contributes to suppressing molecular crystallization and improving yield in the production of an organic electroluminescent device, whereby an organic electroluminescent device having a long lifetime can be obtained, and the aromatic amine derivative is capable of realizing the organic electroluminescent device: where: R1 represents an aryl group or the like; a represents an integer of 0 to 4; b represents an integer of 1 to 3; and at least one of Ar1 to Ar4 represents a group represented by the following general formula (2): where Ar5 represents a fused aromatic ring group and Ar6 represents an aryl group or an aromatic heterocyclic group, where remaining groups of Ar1 to Ar4, none of which is represented by the general formula (2), each independently represent an aryl group or an aromatic heterocyclic group.

DIPROTONATION OF NITROARENES

Cryoscopic measurements shows that 1-nitronaphthalene is diprotonated in trifluoromethanesulfonic acid (TFSA).The diprotonated nitronaphthalenes are N,N-dihydroxyiminiumnaphthalenium dications, wich are fully characterised by UV, 1H-, 13/