58911-02-7 Usage
Uses
Used in Pharmaceutical Industry:
1,2,3,4-Tetrahydronorharmane hydrochloride is used as a potential mood modulator for its effects on the serotonin receptor system in the brain. It may help in managing mood disorders and anxiety due to its influence on neurotransmitter activity.
Used in Neuroprotective Applications:
As an antioxidant and potential neuroprotective agent, 1,2,3,4-Tetrahydronorharmane hydrochloride is used in research for its ability to protect neurons from damage and degeneration, which could be beneficial in the treatment of neurodegenerative diseases.
Used in Research and Development:
1,2,3,4-Tetrahydronorharmane hydrochloride is utilized in scientific research to further understand its effects on mood, anxiety, behavior, and neuroprotection. This research aims to explore its potential therapeutic applications and mechanisms of action, contributing to the development of new treatments for various conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 58911-02-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,9,1 and 1 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 58911-02:
(7*5)+(6*8)+(5*9)+(4*1)+(3*1)+(2*0)+(1*2)=137
137 % 10 = 7
So 58911-02-7 is a valid CAS Registry Number.
InChI:InChI=1/C11H12N2.ClH/c1-2-4-10-8(3-1)9-5-6-12-7-11(9)13-10;/h1-4,12-13H,5-7H2;1H
58911-02-7Relevant academic research and scientific papers
Synthesis of imidazo[1′,5′:1,2]pyrido [3,4-b]indole derivatives
Solymar, Magdolna,Palko, Marta,Martinek, Tamas,Fueloep, Ferenc
, p. 1423 - 1430 (2007/10/03)
The reactions of 1,2,3,4-tetrahydro-β-carboline-1-carboxylic acid and its ethyl ester with alkyl and aryl isothiocyanates under mild conditions resulted in the corresponding thiohydantoin-fused tetrahydro-β-carbolines. Treatment of the ethyl ester with isocyanates furnished ethyl 2-alkyl- or arylcarbamoyl-1,2,3,4-tetrahydro-β-carboline-1-carboxylates which were transformed to hydantoinfused tetrahydro-β-carbolines. The structures of the thiohydantoin compounds, involving two conformers and the presence of keto-enol tautomerism, were determined by NMR spectroscopy.
