474352-95-9 Usage
Chemical class
Heterocyclic compound
Explanation
It is a compound that contains a benzene ring fused to a diazocine ring, which are both heterocyclic structures.
Explanation
The compound has a complex molecular structure with various substituents attached to the carbon atoms of the rings.
Explanation
1,5-Benzodiazocin-4(1H)-one, 2,3,5,6-tetrahydrohas been the subject of research and development as a potential drug candidate for various therapeutic applications.
Explanation
The compound has potential applications in different areas of medicine, although specific applications are not mentioned in the material provided.
Explanation
The chemical and pharmacological properties of 1,5-Benzodiazocin-4(1H)-one, 2,3,5,6-tetrahydromake it a subject of interest for further study in the field of medicinal chemistry and drug discovery.
Explanation
The compound is still under investigation, and its potential as a drug candidate is being explored in various research studies.
Molecular structure
Complex
Pharmacological properties
Potential
Therapeutic applications
Various
Field of interest
Medicinal chemistry and drug discovery
Research status
Ongoing
Check Digit Verification of cas no
The CAS Registry Mumber 474352-95-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,4,3,5 and 2 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 474352-95:
(8*4)+(7*7)+(6*4)+(5*3)+(4*5)+(3*2)+(2*9)+(1*5)=169
169 % 10 = 9
So 474352-95-9 is a valid CAS Registry Number.
474352-95-9Relevant articles and documents
Synthesis of Medium Ring Nitrogen Heterocycles via a Tandem Copper-Catalyzed C-N Bond Formation-Ring-Expansion Process
Klapars, Artis,Parris, Sean,Anderson, Kevin W.,Buchwald, Stephen L.
, p. 3529 - 3533 (2007/10/03)
A simple method for the preparation of medium ring heterocycles (7-, 8-, 9-, and 10-membered) has been developed. The process employs a Cu-catalyzed coupling of a β-lactam with an aryl bromide or iodide followed by intramolecular attack of a pendant amino group. In some instances, the intermediate β-lactam is observable but can be converted to the aza-heterocycle by catalysis. Acetic acid was found to be superior to transition metal complexes as a catalyst for this ring-expansion process.
