784-84-9

Basic information

• Product Name: phenyl(quinolin-8-yl)amine
• Synonyms: phenyl(quinolin-8-yl)amine
• CAS NO: 784-84-9
• Molecular Weight: 220.274
• Mol File: 784-84-9.mol
• Article Data: 14

Chemical Properties

• Melting Point: 121-122 °C
• Boiling Point: 222-223 °C(Press: 12 Torr)
• Density: 1.204±0.06 g/cm3(Predicted)
• CAS DataBase Reference: phenyl(quinolin-8-yl)amine(CAS DataBase Reference)
• NIST Chemistry Reference: phenyl(quinolin-8-yl)amine(784-84-9)
• EPA Substance Registry System: phenyl(quinolin-8-yl)amine(784-84-9)

Safety Data

• Hazardous Substances Data: 784-84-9(Hazardous Substances Data)

Usage

General Description

Phenyl(quinolin-8-yl)amine is an organic compound with the chemical formula C15H12N2. It consists of a phenyl group and a quinoline ring connected to an amine functional group. This chemical compound is widely used in the production of pharmaceuticals and agrochemicals. Its properties make it suitable for various applications in the chemical industry, including as a building block for the synthesis of complex organic molecules and as a component in the production of dyes and pigments. Phenyl(quinolin-8-yl)amine has also shown potential in medicinal research, particularly in the development of new drugs for various diseases. Overall, it is a versatile and valuable chemical with a range of applications in different industries.

Upstream product

• 148-24-3 8-quinolinol 
• 62-53-3 aniline 
• 578-66-5 8-amino quinoline 
• 108-90-7 chlorobenzene 
• 66003-78-9 triphenylsulfonium trifluoromethanesulfonate 
• 394-68-3 8-fluoroquinoline 
• 611-33-6 8-chloroquinoline 
• 33757-48-1 N-quinolin-8-yl-benzamide 
• 1182669-71-1 N-(2-methylbenzoyl)-8-aminoquinoline 
• 98-80-6 phenylboronic acid 
• 16567-18-3 8-bromoquinoline 

Downstream Products

• 1223575-52-7 (N-phenylquinolin-8-amine(-1H))Sc(CH₂SiMe₃)2(THF) 

Relevant articles and documents

Copper-Catalyzed Base-Free N-Arylation of 8-Aminoquinoline Amides through Chelation Assistance

A new and efficient approach for the N-arylation of 8-aminoquinoline amides with diaryliodonium salts has been developed. This chelation-assisted selective C-N cross-coupling reaction gave the desired N-arylated 8-aminoquinoline in moderate to good yields

COMPOUND FOR ORGANIC ELECTRONIC ELEMENT, ORGANIC ELECTRONIC ELEMENT USING THE SAME, AND A ELECTRONIC DEVICE THEREOF

PURPOSE: A compound for an electronic element, an electronic element using the same, and an electronic device thereof are provided to improve light emitting efficiency, thermal resistance, color purity, and lifetime and to lower driving voltage using indoloquinoxaline derivatives. CONSTITUTION: A compound of an organic electronic element contains a compound of chemical formula 1. The organic electronic element has one or more organic layers containing the compound. The organic electronic element comprises a first electrode, the organic layers, and a second electrode. The organic layers are selected among a light emitting layer, a hole injection layer, a hole transport layer, an electron injection layer, and an electron transport layer. An electronic device comprises a display device with the organic electronic element; and a control unit which drives the display device.

Transition-metal-free site-selective C–F bond activation for synthesis of 8-aminoquinolines

An efficient and general selective method for the synthesis of 8-aminoquinoline derivatives has been disclosed through transition metal direct C–N coupling from fluoroquinolines and arylamines. Significantly, good chemo- and regio-selectivity was observed