120218-45-3 Usage
Uses
Used in Pharmaceutical Research:
1-Phenylcyclobutylamine hydrochloride is used as a research chemical for studying its effects on the central nervous system, particularly its role as a selective serotonin releasing agent. This is crucial for understanding its potential in the development of treatments for depression and anxiety.
Used in Neuroscience:
In the field of neuroscience, 1-Phenylcyclobutylamine hydrochloride is used as a tool to explore the mechanisms of serotonin release and its impact on mood regulation, providing insights into the neurobiological basis of mood disorders.
Used in Drug Development:
1-Phenylcyclobutylamine hydrochloride is utilized in the development of new pharmaceuticals targeting mood disorders. Its properties as a SSRA make it a candidate for further research into more effective and safer treatments for depression and anxiety.
Used in Toxicology and Safety Assessments:
In toxicology, 1-Phenylcyclobutylamine hydrochloride is used to evaluate the safety and potential side effects of this class of compounds, ensuring that future drugs developed from this research are both effective and safe for human use.
Check Digit Verification of cas no
The CAS Registry Mumber 120218-45-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,2,1 and 8 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 120218-45:
(8*1)+(7*2)+(6*0)+(5*2)+(4*1)+(3*8)+(2*4)+(1*5)=73
73 % 10 = 3
So 120218-45-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H13N.ClH/c11-10(7-4-8-10)9-5-2-1-3-6-9;/h1-3,5-6H,4,7-8,11H2;1H
120218-45-3Relevant academic research and scientific papers
Synthesis method of arylcyclobutane compound
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Paragraph 0206-0208; 0237-0240, (2022/01/10)
The present invention discloses a method for synthesizing an arylcyclobutane compound to 1eq phenylacetonitrile and 1.1eq 1-bromo-3-chloropropane as raw material, N,N- dimethylacetamide as a solvent, plus 2.5eq sodium hydride, under the protection of iner