84500-68-5

Basic information

• Product Name: 1-(1,2,3,4-tetrahydroisoquinolin-1-yl)-1,2,3,4-tetrahydroisoquinoline
• CAS NO: 84500-68-5
• Molecular Formula: C₁₈H₂₀N₂
• Mol File: 84500-68-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1-(1,2,3,4-tetrahydroisoquinolin-1-yl)-1,2,3,4-tetrahydroisoquinoline(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(1,2,3,4-tetrahydroisoquinolin-1-yl)-1,2,3,4-tetrahydroisoquinoline(84500-68-5)
• EPA Substance Registry System: 1-(1,2,3,4-tetrahydroisoquinolin-1-yl)-1,2,3,4-tetrahydroisoquinoline(84500-68-5)

Safety Data

• Hazardous Substances Data: 84500-68-5(Hazardous Substances Data)

Usage

General Description

1-(1,2,3,4-tetrahydroisoquinolin-1-yl)-1,2,3,4-tetrahydroisoquinoline is a chemical compound with a complex structure consisting of two tetrahydroisoquinoline groups connected by a single nitrogen atom. It is a heterocyclic compound with potential pharmacological significance. The molecule's intricate structure suggests it may have unique chemical properties and potential biological activities. Further research is needed to fully understand the potential uses and effects of this compound.

Upstream product

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

Relevant articles and documents

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 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