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4-Aminoquinoline
Names
	IUPAC name Quinolin-4-amine
Identifiers
CAS Number	578-68-7 ;
3D model (JSmol)	Interactive image;
ChEMBL	ChEMBL58146 ;
ChemSpider	61751 ;
PubChem CID	68476;
UNII	GTE5P5L97N ;
	InChI InChI=1S/C9H8N2/c10-8-5-6-11-9-4-2-1-3-7(8)9/h1-6H,(H2,10,11) Key: FQYRLEXKXQRZDH-UHFFFAOYSA-N ; InChI=1S/C9H8N2/c10-8-5-6-11-9-4-2-1-3-7(8)9/h1-6H,(H2,10,11);
	SMILES n1ccc(c2ccccc12)N;
Properties
Chemical formula	C9H8N2
Molar mass	144.177 g·mol−1
Appearance	Powder to crystalline, White/Yellow/Orange
Melting point	151.0 to 155.0 °C
Hazards
	Occupational safety and health (OHS/OSH):
Main hazards	Causes skin and serious eye irritation
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

4-Aminoquinoline

4-Aminoquinoline is a form of aminoquinoline with the amino group at the 4-position of the quinoline. The compound has been used as a precursor for the synthesis of its derivatives. ^[1]

A variety of derivatives of 4-aminoquinoline are antimalarial agents useful in treating erythrocytic plasmodial infections.^[2] Examples include amodiaquine, chloroquine, and hydroxychloroquine. Other uses for the derivatives are: anti-asthmatic, antibacterial, anti-fungal, anti-malarial, antiviral and anti-inflammatory agents.^[1]

A patent application for 4-aminoquinoline compounds was filed in 2002 and published in 2005.^[3]