100561-34-0 Usage
Uses
Used in Pharmaceutical Industry:
2,2a,3,4-tetrahydro-Benz[cd]indol-5(1H)-one is used as a serotonin receptor agonist for the treatment of disorders such as anxiety, depression, and addiction. Its interaction with serotonin receptors may help modulate mood and behavior, providing therapeutic benefits for individuals suffering from these conditions.
Used in Neurodegenerative Disease Research:
In the field of neurodegenerative diseases, 2,2a,3,4-tetrahydro-Benz[cd]indol-5(1H)-one is utilized for its antioxidant and neuroprotective properties. Its potential to protect neurons from oxidative stress and other damaging processes may contribute to the development of therapies for conditions such as Alzheimer's disease and Parkinson's disease.
Used in Organic Synthesis and Drug Discovery:
2,2a,3,4-tetrahydro-Benz[cd]indol-5(1H)-one serves as a key intermediate in the synthesis of other biologically active molecules. Its unique structure and functional groups make it a valuable building block for the development of new pharmaceutical agents, enhancing the scope of organic synthesis and drug discovery efforts.
Used in Chemical Research:
2,2a,3,4-tetrahydro-Benz[cd]indol-5(1H)-one is also used as a subject of study in chemical research to explore its properties, reactivity, and potential applications in various chemical processes. Understanding its behavior in different chemical environments can lead to the discovery of new reactions and the development of novel synthetic routes for the production of pharmaceuticals and other bioactive compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 100561-34-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,5,6 and 1 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 100561-34:
(8*1)+(7*0)+(6*0)+(5*5)+(4*6)+(3*1)+(2*3)+(1*4)=70
70 % 10 = 0
So 100561-34-0 is a valid CAS Registry Number.
100561-34-0Relevant academic research and scientific papers
Dehydrogenation with Benzeneseleninic Anhydride in the Total Synthesis of Ergot Alkaloids
Ninomiya, Ichiya,Hashimoto, Chiyomi,Kiguchi, Toshiko,Naito, Takeaki,Barton, Derek, H. R.,et al.
, p. 707 - 713 (2007/10/02)
Investigation of the dehydrogenative conversion of indolines into indoles with benzeneseleninic anhydride (1) resulted in the development of an efficient standardised procedure, which was successfully applied to the final steps in first total synthesis of (+/-)-lysergol (18), (+/-)-isolysergol (27), and (+/-)-elymoclavine (29).
