84500-68-5

Usage

Uses

Used in Pharmaceutical Industry:
1-(1,2,3,4-tetrahydroisoquinolin-1-yl)-1,2,3,4-tetrahydroisoquinoline is used as a potential pharmaceutical compound for its possible unique chemical properties and biological activities. 1-(1,2,3,4-tetrahydroisoquinolin-1-yl)-1,2,3,4-tetrahydroisoquinoline's complex structure may offer novel therapeutic applications once its pharmacological profile is fully understood.
Used in Chemical Research:
In the field of chemical research, 1-(1,2,3,4-tetrahydroisoquinolin-1-yl)-1,2,3,4-tetrahydroisoquinoline serves as a subject of study for its complex structure and potential to reveal new insights into heterocyclic chemistry and its applications.

Upstream product

• 84500-67-4 1,2,3,4-tetrahydroisoquinoline-1-carbonitrile 
• 3230-65-7 3,4-dihydroisoquinoline 
• 14040-79-0 N¹, N²-diphenethyloxalamide 
• 34786-39-5 3,3′,4,4′-tetrahydro-1,1′-biisoquinoline 
• 64-04-0 phenethylamine 
• 23069-99-0 N-(2-phenylethyl)formamide 

Relevant academic research and scientific papers

Design aspects of metal-free nitrogen-based catalysts and their influence on the yield in the Henry reaction

Design aspects of metal-free nitrogen-based catalysts and their influence on the yield in the Henry reaction are disclosed. C 1-Symmetric, N,N-1,2-disposed amine-imine type catalysts were found to be most efficient. C 1-N,N-1,2-Disposed 1,2,3,4-tetrahydro-1,1′-biisoquinoline selectively and efficiently catalyzed the addition of nitromethane to α-keto esters and aldehydes giving exclusively the corresponding β-nitro alcohol adducts in excellent yields under very mild conditions. Georg Thieme Verlag Stuttgart New York.

Synthesis and reactions of partially reduced biisoquinolines

An improved synthesis of the 1,1′,2,2′,3,3′,4,4′-octahydro-1,1′-biisoquinoline ring system is described. The reactivity of this system has been investigated, including the unusually high basicity of the parent compound and its N,N′-dimethyl derivative. The resolution of the parent compound has been achieved for the first time, along with the development of a straightforward method for assaying its enantiomeric purity.

Synthesis of 1-(Aminomethyl)-1,2,3,4-tetrahydroisoquinolines and Their Actions at Adrenoceptors in Vivo and in Vitro

An improved synthesis of 1-(aminomethyl)-1,2,3,4-tetrahydroisoquinolines has been developed by using aluminum hydride reduction of 1-cyano-1,2,3,4-tetrahydroisoquinolines.Three 1-(aminomethyl)-6,7-dihydroxytetrahydroisnolines