104924-34-7

Basic information

• Product Name: Isoquinoline, 1-(4-chlorophenyl)-
• CAS NO: 104924-34-7
• Molecular Formula: C15H10ClN
• Molecular Weight: 239.704
• Mol File: 104924-34-7.mol

Chemical Properties

• CAS DataBase Reference: Isoquinoline, 1-(4-chlorophenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Isoquinoline, 1-(4-chlorophenyl)-(104924-34-7)
• EPA Substance Registry System: Isoquinoline, 1-(4-chlorophenyl)-(104924-34-7)

Safety Data

• Hazardous Substances Data: 104924-34-7(Hazardous Substances Data)

Upstream product

• 104924-33-6 2-(4-chlorobenzamido)-1-phenyl-1-ethanol 
• 106-39-8 bromochlorobenzene 
• 1532-72-5 isoquinoline N-oxide 
• 119-65-3 isoquinoline 
• 106-47-8 4-chloro-aniline 

Downstream Products

• 1443309-00-9 C₂₆H₂₃ClNO₂⁽¹⁺⁾*Br^(1-) 

Relevant articles and documents

Phase-selective modulation of TiO2 for visible light-driven C–H arylation: Tuning of absorption and adsorptivity

To understand and modify TiO2 for organic photoreaction, two points are important: improving light absorption and retaining adsorption sites for organic reagents. Herein, we tuning the absorption and adsorption of TiO2 by introducing

Method for solvent accelerated selective dehydrogenation of tetrahydroisoquinoline type compound

The invention discloses a method for synthesizing 1-substituted-3,4-dihydroisoquinoline through the solvent accelerated selective partial dehydrogenation of a 1-substituted-1,2,3,4-tetrahydroisoquinoline compound. For a simple and easily obtained cyclic amine type compound such as a tetrahydroisoquinoline compound, a corresponding imine compound can be obtained through selective dehydrogenation; the conversion ratio of the cyclic amine type compound is higher; further, the proportion of a partially dehydrogenated product to a fully dehydrogenated product is more than 20 to 1. The method is simple and convenient to operate, is practical, easy and feasible, and is mild in reaction condition; the actual cost is greatly reduced. In addition, a method for synthesizing 3,4-dihydroisoquinoline through the direct dehydrogenation of tetrahydroisoquinoline has the advantages of atom economy and environmental friendliness.

ISOQUINOLINE SYNTHESES VIA 2-OXAZOLINES. PART V. SYNTHESES OF 4-ALKYL-1-PHENYLISOQUINOLINES BY PICTET-GAMS REACTION

Conditions necessary for transformation of hydroxyamides (4) and 2-oxazolines (5) into 4-alkyl-1-phenylisoquinolines have been established.The mechanism of the Pictet-Gams reaction claiming the existence of protonated oxazolines (7) and unsaturated amides