17507-24-3

Basic information

• Product Name: 2-Isopropylquinoline
• Synonyms: 2-Isopropylquinoline
• CAS NO: 17507-24-3
• Molecular Formula: C₁₂H₁₃N
• Molecular Weight: 171.24
• Mol File: 17507-24-3.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-Isopropylquinoline(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Isopropylquinoline(17507-24-3)
• EPA Substance Registry System: 2-Isopropylquinoline(17507-24-3)

Safety Data

• Hazardous Substances Data: 17507-24-3(Hazardous Substances Data)

Usage

Synthesis Reference(s)

The Journal of Organic Chemistry, 30, p. 4311, 1965 DOI: 10.1021/jo01023a505

Upstream product

• 5344-90-1 2-Aminobenzyl alcohol 
• 598-75-4 3-methyl-2-butanol 
• 53627-32-0 2-isopropyl-1,2,3,4-tetrahydroquinoline 
• 563-79-1 2,3-Dimethyl-2-butene 
• 2637-37-8 Quinoline-2-thione 

Downstream Products

• 608525-30-0 (R)-2-isopropyl-1,2,3,4-tetrahydroquinoline 
• 1011-47-8 1-quinolin-2-yl-ethanone 
• 608525-30-0 (S)-2-isopropyl-1,2,3,4-tetrahydroquinoline 
• 55904-64-8 2-isopropyl-5,6,7,8-tetrahydroquinoline 
• 53627-32-0 2-isopropyl-1,2,3,4-tetrahydroquinoline 

Relevant articles and documents

Synthesis of Tetrahydroquinolines via Borrowing Hydrogen Methodology Using a Manganese PN3Pincer Catalyst

A straightforward and selective synthesis of 1,2,3,4-tetrahydroquinolines starting from 2-aminobenzyl alcohols and simple secondary alcohols is reported. This one-pot cascade reaction is based on the borrowing hydrogen methodology promoted by a manganese(I) PN3 pincer complex. The reaction selectively leads to 1,2,3,4-tetrahydroquinolines thanks to a targeted choice of base. This strategy provides an atom-efficient pathway with water as the only byproduct. In addition, no further reducing agents are required.

Photoaddition of Olefins to Quinolin-, Isoquinolin- and Phthalazin-thione Systems

Irradiation of quinolin-2-, isoquinolin-1-, and phthalazin-1-thiones with olefins afforded photoaddition products: substituted quinolines, isoquinolines and phthalazines at the thiocarbonyl carbon.A new addition-cyclization was found producing tricyclic thiopyrano-isoquinolines and -phthalazines.