54504-51-7 Usage
Uses
Used in Pharmaceutical Applications:
1-acetyl-4-(2-chloroethyl)piperazine is used as a research compound for the development of new psychiatric medications due to its mild sedative and anxiolytic effects. It is of interest in the field of medicinal chemistry for drug discovery and development.
Used in Central Nervous System Disorders Treatment:
In the medical field, 1-acetyl-4-(2-chloroethyl)piperazine is used as a potential treatment for central nervous system disorders, leveraging its pharmacological properties to address neurological conditions.
Used in Anticancer and Anti-tumor Research:
1-acetyl-4-(2-chloroethyl)piperazine is used as a subject of study in cancer research for its potential anti-tumor and anti-cancer properties, indicating its broad range of applications in oncology and contributing to the advancement of cancer therapies.
Used in Research and Development:
In the scientific community, 1-acetyl-4-(2-chloroethyl)piperazine is utilized as a versatile compound in research and development, exploring its diverse potential uses in medicine and science to enhance understanding and innovation in these fields.
Check Digit Verification of cas no
The CAS Registry Mumber 54504-51-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,5,0 and 4 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 54504-51:
(7*5)+(6*4)+(5*5)+(4*0)+(3*4)+(2*5)+(1*1)=107
107 % 10 = 7
So 54504-51-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H15ClN2O/c1-8(12)11-6-4-10(3-2-9)5-7-11/h2-7H2,1H3
54504-51-7Relevant academic research and scientific papers
SUBSTITUTED TRIAZOLE DERIVATIVES AS OXYTOCIN ANTAGONISTS
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Page/Page column 100, (2010/02/13)
The present invention relates to a class of substituted triazoles of formula (I) with activity as oxytocin antagonists, uses thereof, processes for the preparation thereof and compositions containing said inhibitors. These inhibitors have utility in a variety of therapeutic areas including sexual dysfunction, particularly premature ejaculation (P.E.).
Hexahydro-trans- and tetrahydropyridoindole neuroleptic agents
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, (2008/06/13)
Derivatives of 2,3,4,5-tetrahydro-1H-pyrido[4,3-b]-indole and of (+)enantiomeric, mixtures of (+) and (-)enantiomeric or (±)racemic 2,3,4,4a,5,9b-hexahydro-4a,9b-trans-1H-pyrido[4,3-b]indole, substituted at the 5-position with an aryl group and at the 2-p
