1567-30-2 Usage
Heterocyclic Compound
Yes
Explanation
A heterocyclic compound is a cyclic compound containing atoms of at least two different elements. In this case, the compound has a seven-membered diazocine ring with four carbon atoms and three nitrogen atoms.
Explanation
The compound has a diazocine ring, which is a seven-membered ring containing three nitrogen atoms.
Explanation
The compound is also known by the name octahydrodiphenazine, which is another way to describe its structure.
Explanation
The compound is used in different research applications, including the study of its potential biological activities.
Explanation
Studies have shown that 1,2-Diazocine, 4,5,6,7-tetrahydro-3,8-diphenylexhibits antitumor and antimicrobial properties, making it a potential candidate for further research in the development of new drugs.
Explanation
The compound is used as a building block in the synthesis of other organic compounds, which can be useful in various chemical and pharmaceutical applications.
Ring Structure
Seven-membered diazocine ring
Substituents
4,5,6,7-tetrahydro and 3,8-diphenyl
Synonyms
Octahydrodiphenazine
Research Applications
Various
Biological Activities
Antitumor and antimicrobial properties
Synthesis
Building block for other organic compounds
Check Digit Verification of cas no
The CAS Registry Mumber 1567-30-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,6 and 7 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1567-30:
(6*1)+(5*5)+(4*6)+(3*7)+(2*3)+(1*0)=82
82 % 10 = 2
So 1567-30-2 is a valid CAS Registry Number.
1567-30-2Relevant academic research and scientific papers
Synthesis of Stable 1,2-Diazocines, 4,7-Disubstituted 3,8-Diaryl-1,2-diazacycloocta-2,4,6,8-tetraenes and Their Thermolysis
Yogi, Seiichi,Hokama, Kozo,Ueno, Kazunori,Tsuge, Otohiko
, p. 1087 - 1094 (2007/10/02)
Stable 1,2-diazocines, 3,8-diaryl-4,6-dichloro-1,2-diazacycloocta-2,4,6,8-tetraenes, were prepared via a chlorination-dehydrochlorination sequence starting from readily-available 3,8-diaryl-1,2-diazacycloocta-2,4-dienes.When reacted with metal caroxylates in benzene under reflux, the dichloro-1,2-diazocines were converted into stable 4-acyloxy- and/or 4,7-is(acyloxy)-1,2-diazocines.On the thermolysis in toluene under reflux, all the diazocines gave only pyridine derivatives with extrusion of the corresponding benzonitriles.The thermal behavior of the diazocines are also discussed.
