20668-43-3

Basic information

• Product Name: 3-propylquinoline
• Synonyms: 3-propylquinoline
• CAS NO: 20668-43-3
• Molecular Formula: C12H13N
• Molecular Weight: 171.24
• Mol File: 20668-43-3.mol
• Article Data: 3

Chemical Properties

• Melting Point: 187 °C
• Boiling Point: 280.9°Cat760mmHg
• Flash Point: 115.4°C
• Appearance: /
• Density: 1.03g/cm³
• Vapor Pressure: 0.00628mmHg at 25°C
• Refractive Index: 1.594
• PKA: 5.19±0.11(Predicted)
• CAS DataBase Reference: 3-propylquinoline(CAS DataBase Reference)
• NIST Chemistry Reference: 3-propylquinoline(20668-43-3)
• EPA Substance Registry System: 3-propylquinoline(20668-43-3)

Safety Data

• Hazardous Substances Data: 20668-43-3(Hazardous Substances Data)

Usage

InChI:InChI=1/C12H13N/c1-2-5-10-8-11-6-3-4-7-12(11)13-9-10/h3-4,6-9H,2,5H2,1H3

Upstream product

• 77-99-6 1,1,1-tri(hydroxymethyl)propane 
• 7664-93-9 sulfuric acid 
• 98-95-3 nitrobenzene 
• 62-53-3 aniline 
• 5332-24-1 3-bromoquinoline 
• 22971-32-0 1-(pyridin-2-yl)butan-1-one 
• 5344-90-1 2-Aminobenzyl alcohol 
• 110-62-3 pentanal 

Relevant articles and documents

Pd-Catalyzed Alkylation of (Iso)quinolines and Arenes: 2-Acylpyridine Compounds as Alkylation Reagents

The first Pd-catalyzed alkylation of (iso)quinolines and arenes is reported. The readily available and bench-stable 2-acylpyridine compounds were used as an alkylation reagent to form the structurally versatile alkylated (iso)quinolines and arenes. The method affords a convenient pathway for the introduction of alkyl groups into organic molecules.

A copper(II)-catalyzed protocol for modified Friedl?nder quinoline synthesis

2-Aminobenzyl alcohol reacts with an array of ketones in dioxane at 100 °C in the presence of a catalytic amount of CuCl2 along with KOH under O2 atmosphere to afford the corresponding quinolines in good yields. 2-Aminobenzyl alcohol is also oxidatively coupled and cyclized with various aldehydes by step-by-step procedure, an initial treatment of 2-aminobenzyl alcohol in the presence of CuCl2 and KOH in dioxane under O2 atmosphere and subsequent addition of aldehyde to the mixture followed by stirring under argon atmosphere, to give 3-substituted quinolines in moderate to good yields.