22964-00-7 Usage
Uses
Used in Scientific Research:
Benzo(b)thiophene-3-ethylamine, 5-bromo-, hydrochloride serves as a valuable compound in scientific research for its unique molecular structure and potential reactivity. It is used as a research chemical to explore its properties and interactions with other compounds, which can contribute to the development of new methodologies or understanding of chemical reactions.
Used in Biochemistry:
In the field of biochemistry, Benzo(b)thiophene-3-ethylamine, 5-bromo-, hydrochloride may be employed as a tool to study its interactions with biological molecules. Its specific functional groups could potentially allow it to bind to or modify biomolecules, providing insights into biological processes or the development of bioactive compounds.
Used in Pharmacology:
Benzo(b)thiophene-3-ethylamine, 5-bromo-, hydrochloride may also have applications in pharmacology, where it could be investigated for its potential as a therapeutic agent or a lead compound in drug discovery. Its unique structure and functional groups might offer specific binding affinities or activities against biological targets, which could be harnessed for the treatment of various conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 22964-00-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,9,6 and 4 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 22964-00:
(7*2)+(6*2)+(5*9)+(4*6)+(3*4)+(2*0)+(1*0)=107
107 % 10 = 7
So 22964-00-7 is a valid CAS Registry Number.
22964-00-7Relevant academic research and scientific papers
5-Halobenzothiophene analogues of melatonin: Synthesis and affinity for mt1 and MT2 receptors in man
Leclerc,Beaurain,Depreux,Bennejean,Delagrange,Boutin,Lesieur
, p. 61 - 65 (2007/10/03)
A novel series of melatonin analogues based on the benzothiophene nucleus is described. In these compounds the methoxy group was replaced by electron-attracting groups such halogens (Br and Cl) with the aim of supplementing structure-affinity relationship
