104465-76-1 Usage
Chemical compound
2-(1,2,3,4-tetrahydroisoquinolin-4-yl)ethanol is a chemical compound.
Pharmacological properties
The compound has potential pharmacological properties and has been studied for its potential as a central nervous system depressant and analgesic agent.
Derivative of tetrahydroisoquinoline
It is a derivative of tetrahydroisoquinoline, a class of compounds found in various natural products.
Interaction with neurotransmitter receptors
Its structure suggests that it may interact with neurotransmitter receptors in the brain.
Potential medical applications
The compound may have applications in the treatment of pain and other neurological disorders, and it has been the subject of research for its potential as a therapeutic agent for conditions such as Parkinson's disease and addiction.
Further investigation needed
Further investigation is needed to fully understand the pharmacological properties and potential medical applications of 2-(1,2,3,4-tetrahydroisoquinolin-4-yl)ethanol.
Check Digit Verification of cas no
The CAS Registry Mumber 104465-76-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,4,6 and 5 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 104465-76:
(8*1)+(7*0)+(6*4)+(5*4)+(4*6)+(3*5)+(2*7)+(1*6)=111
111 % 10 = 1
So 104465-76-1 is a valid CAS Registry Number.
104465-76-1Relevant articles and documents
Synthesis of 4-Vinyl-1,2,3,4-tetrahydroisoquinoline from N-Tethered Benzyl-Alkenol Catalyzed by Indium(III) Chloride: Formal Synthesis of (±)-Isocyclocelabenzine
Behera, Bipin Kumar,Devi, Ngangbam Renubala,Saikia, Anil K.,Shit, Sudip
, p. 1425 - 1434 (2020/04/27)
An intramolecular Friedel-Crafts cyclization reaction catalyzed by indium(III) chloride for the formation of 4-vinyl-1,2,3,4-tetrahydroisoquinoline from N-tethered benzyl-alkenol in good yields has been described. The reaction is highly regioselective and generates an exocyclic vinyl functionality in the piperidine ring. The reaction is compatible with a wide range of functional groups. The strategy is demonstrated for the formal synthesis of (±)-isocyclocelabenzine alkaloid.
