58349-15-8 Usage
Uses
Used in Pharmaceutical Research and Drug Development:
(R)-5-Methoxy-1,2,3,4-tetrahydronaphthalen-2-aMine (Hydrochloride) is used as a research compound for its potential psychoactive and hallucinogenic effects. It is being studied for its potential use in the treatment of mood disorders and psychiatric conditions, offering a promising avenue for developing novel therapeutic agents.
Used in Mood Disorder Treatment:
In the field of mood disorder treatment, (R)-5-Methoxy-1,2,3,4-tetrahydronaphthalen-2-aMine (Hydrochloride) is used as a potential therapeutic agent for its psychoactive properties. It is being investigated for its ability to modulate mood and alleviate symptoms associated with various mood disorders, providing a new approach to treatment.
Used in Psychiatric Condition Management:
(R)-5-Methoxy-1,2,3,4-tetrahydronaphthalen-2-aMine (Hydrochloride) is utilized as a potential treatment for psychiatric conditions due to its hallucinogenic effects. It is being explored for its capacity to influence neural pathways and cognitive processes, offering a novel perspective in the management of psychiatric disorders.
Used in Drug Formulation:
In the pharmaceutical industry, (R)-5-Methoxy-1,2,3,4-tetrahydronaphthalen-2-aMine (Hydrochloride) is used as a key ingredient in drug formulations. Its increased stability and solubility in the hydrochloride form make it an ideal candidate for developing effective and stable medications for various therapeutic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 58349-15-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,3,4 and 9 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 58349-15:
(7*5)+(6*8)+(5*3)+(4*4)+(3*9)+(2*1)+(1*5)=148
148 % 10 = 8
So 58349-15-8 is a valid CAS Registry Number.
58349-15-8Relevant academic research and scientific papers
Alternative and straightforward synthesis of dopaminergic 5-methoxy-1,2,3,4-tetrahydronaphthalen-2-amine
Oeztaskin, Necla,Goeksu, Sueleyman,Hasan Secen
, p. 2017 - 2024 (2011/06/24)
5-Methoxy-1,2,3,4-tetrahydronaphthalen-2-amine was synthesized from 2-naphthoic acid in six steps with an overall yield of 27%. Following the reaction sequence, bromination, esterification, substitution with NaOMe in the presence of CuI, the Birch reducti
α-Adrenergic Agents. 2. Synthesis and α1-Agonist Activity of 2-Aminotetralins
DeMarinis, R. M.,Shah, D. H.,Hall, R. F.,Hieble, J. P.,Pendleton, R. G.
, p. 136 - 141 (2007/10/02)
Substituted 2-aminotetralins are potent, selective, direct-acting agonists as postjunctional α1 receptors.Within this series, substituent alterations on the ring, as well as on the nitrogen, change the potency of compounds by over three orders
