20069-08-3 Usage
Uses
Used in Pharmaceutical Applications:
1-(2-Pyrrolizinoethyl)-1,2,3,4-tetrahydro-β-carboline is used as a compound of interest for its potential psychoactive properties and effects on neurotransmitter systems. Its investigation into the central nervous system makes it a candidate for the development of new medications targeting neurological disorders and conditions.
Used in Neurotoxicology Research:
In the field of neurotoxicology, 1-(2-Pyrrolizinoethyl)-1,2,3,4-tetrahydro-β-carboline is used as a subject of study for its potential involvement in the formation of neurotoxic compounds. Understanding its role in neurotoxicity can contribute to the development of strategies to mitigate or prevent neurodegenerative diseases and other conditions related to neurotoxicity.
Used in Medicinal Chemistry Research:
1-(2-Pyrrolizinoethyl)-1,2,3,4-tetrahydro-β-carboline is utilized as a key compound in medicinal chemistry research, where its unique structure and pharmacological properties are explored for the development of novel therapeutic agents. 1-(2-Pyrrolizinoethyl)-1,2,3,4-tetrahydro-β-carboline's interaction with neurotransmitter systems and its effects on the central nervous system make it a valuable tool in the search for new drugs to treat various neurological and psychiatric conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 20069-08-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,0,6 and 9 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 20069-08:
(7*2)+(6*0)+(5*0)+(4*6)+(3*9)+(2*0)+(1*8)=73
73 % 10 = 3
So 20069-08-3 is a valid CAS Registry Number.
20069-08-3Relevant academic research and scientific papers
6′,7′-Dihydrokeramamine C and analogues: Synthesis and biological evaluation
Pouilhès, Annie,Duval-Lungulescu, Monica,Lambel, Stéphanie,Léonce, Stéphane,Langlois, Yves
, p. 8297 - 8299 (2007/10/03)
6′,7′-Dihydrokeramamine C 7d and analogues have been synthesised and evaluated for their cytotoxicity. Compound 7f in which the azacycloundecane ring has been substituted by a dihexylamino unit showed increasing biological activity.
A PRACTICAL SYNTHESIS OF (+/-)-ELAEOCARPIDINE
Gribble, Gordon W.,Switzer, Frank L.
, p. 377 - 384 (2007/10/02)
The Elaeocarpus densiflorus indole alkaloid (+/-)-elaeocarpidine (1) is synthesized in five steps and 31percent yield from the commercially available materials 2-(2-bromoethyl)-1,3-dioxolane, ethyl 4-bromobutyrate, and tryptamine hydrochloride (7).The key step is a diisobutylaluminum hydride reductive cyclization of amine lactam 8 to give 1 in 86percent yield.
