27969-93-3 Usage
Uses
Used in Pharmaceutical Research:
(1Z)-1-[(2,6-dimethylphenyl)hydrazono]naphthalen-2(1H)-one is utilized as a research compound for investigating its anti-inflammatory and anti-cancer properties. Its unique structure allows scientists to explore its potential as a therapeutic agent, particularly in the treatment of various cancers and inflammatory conditions.
Used in Organic Synthesis:
In the field of organic synthesis, (1Z)-1-[(2,6-dimethylphenyl)hydrazono]naphthalen-2(1H)-one is employed as a chemical building block. Its structural features make it a valuable component in the creation of more complex organic molecules, contributing to the advancement of chemical research and the development of novel compounds with diverse applications.
Used in Structure-Activity Relationship Studies:
(1Z)-1-[(2,6-dimethylphenyl)hydrazono]naphthalen-2(1H)-one is used as a reference compound in structure-activity relationship studies. By examining the effects of its molecular structure on biological activity, researchers can gain insights into the design of more effective pharmaceuticals and chemical compounds with similar properties.
Check Digit Verification of cas no
The CAS Registry Mumber 27969-93-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,9,6 and 9 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 27969-93:
(7*2)+(6*7)+(5*9)+(4*6)+(3*9)+(2*9)+(1*3)=173
173 % 10 = 3
So 27969-93-3 is a valid CAS Registry Number.
27969-93-3Relevant academic research and scientific papers
New dry arenediazonium salts, stabilized to an exceptionally high degree by the anion of o-benzenedisulfonimide
Barbero, Margherita,Crisma, Marco,Degani, Lacopo,Fochi, Rita,Perracino, Paolo
, p. 1171 - 1175 (2007/10/03)
Arenediazonium o-benzenedisulfonimides 3 (20 examples, yield >90%) were prepared in the dry state by diazotization of aromatic amines with (-pentyl nitrite and o-benzenedisulfonimide in glacial acetic acid or formic acid at 0-5°C. Unlike most diazonium salts in the dry state, salts 3 are very highly stable.
