2508-86-3

Basic information

• Product Name: 4-aminoquinoline-1-oxide
• Synonyms: 4-aminoquinoline-1-oxide
• CAS NO: 2508-86-3
• Molecular Formula: C9H8 N2 O
• Molecular Weight: 160.19
• Mol File: 2508-86-3.mol
• Article Data: 3

Chemical Properties

• Melting Point: 272°C (rough estimate)
• Boiling Point: 286.07°C (rough estimate)
• Flash Point: 135.6°C
• Appearance: /
• Density: 1.1846 (rough estimate)
• Vapor Pressure: 0.000492mmHg at 25°C
• Refractive Index: 1.5570 (estimate)
• CAS DataBase Reference: 4-aminoquinoline-1-oxide(CAS DataBase Reference)
• NIST Chemistry Reference: 4-aminoquinoline-1-oxide(2508-86-3)
• EPA Substance Registry System: 4-aminoquinoline-1-oxide(2508-86-3)

Safety Data

• Hazardous Substances Data: 2508-86-3(Hazardous Substances Data)

Usage

Safety Profile

Mutation data reported. Whenheated to decomposition it emits toxic fumes of NOx.

InChI:InChI=1/C9H8N2O.ClH/c10-8-5-6-11(12)9-4-2-1-3-7(8)9;/h1-6,10,12H;1H/b10-8+;

Upstream product

• 1613-37-2 Quinoline N-oxide 
• 578-68-7 4-aminoquinoline 
• 56-57-5 4-nitroquinoline-N-oxide 
• 2669-36-5 4-quinolyl azide N-oxide 
• 4637-59-6 4-Chloroquinoline N-oxide 

Downstream Products

• 22615-00-5 3-bromoquinoline N-oxide 
• 21236-85-1 quinoline-4-carbonitrile 1-oxide 
• 4637-59-6 4-Chloroquinoline N-oxide 
• 80947-25-7 2-chloroquinoline-4-amine 

Relevant articles and documents

Concerning Model Metabolites of the Carcinogen 4-Nitroquinoline 1-Oxide. Reactivity and Solvolytic Behavior of 1-Hydroxy-4-(acetoxyimino)-1,4-dihydroquinoline

1-Hydroxy-4-(acetoxyimino)-1,4-dihydroquinoline is obtained quantitatively by reaction of 1-acetoxy-4-(acetoxyimino)-1,4-dihydroquinoline with piperidine in dimethyl sulfoxide.Spectroscopic results establish that this monoacetate exists preferentially as

KINETICS OF N-OXIDATION OF COMPOUNDS OF THE QUINOLINE SERIES AND ISOMERIC BENZOQUINOLINES BY PERBENZOIC ACID IN CHLOROFORM AND AQUEOUS DIOXANE

The kinetics of the N-oxidation with perbenzoic acid of 15 derivatives of quinoline and benzoquinoline in chloroform and 19 compounds in 50percent aqueous dioxane at 20, 25, 30, and 35 deg C were subjected to a comparative study.The rate constants, parameters of Arrhenius equation, and the activation energies for the N-oxidation of the indicated monoazines were determined.A scale of the reactivities of derivatives of the quinoline series and benzoquinolines was calculated within the framework of general perturbation theory.