2922-11-4 Usage
Uses
Used in Chemical Research:
2,2'-Pyridylisatogen is used as a spin trap for the hydroxyl radical. It is particularly useful in the study of free radicals and reactive oxygen species, which are important in various chemical reactions and biological processes.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2,2'-pyridylisatogen is used as an intermediate in the synthesis of various drugs and pharmaceutical compounds. Its unique chemical properties make it a valuable building block for the development of new medications.
Used in Material Science:
2,2'-Pyridylisatogen is also used in material science for the development of new materials with specific properties. Its ability to form complexes with various metal ions makes it a useful component in the design of new catalysts and other materials with unique chemical and physical properties.
Check Digit Verification of cas no
The CAS Registry Mumber 2922-11-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,2 and 2 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2922-11:
(6*2)+(5*9)+(4*2)+(3*2)+(2*1)+(1*1)=74
74 % 10 = 4
So 2922-11-4 is a valid CAS Registry Number.
InChI:InChI=1/C13H8N2O2/c16-13-9-5-1-2-7-11(9)15(17)12(13)10-6-3-4-8-14-10/h1-8H
2922-11-4Relevant academic research and scientific papers
A combined experimental and density functional theory study on the Pd-mediated cycloisomerization of o-alkynylnitrobenzenes - Synthesis of isatogens and their evaluation as modulators of ROS-mediated cell death
Ramana, Chepuri V.,Patel, Pitambar,Vanka, Kumar,Miao, Benchun,Degterev, Alexei
experimental part, p. 5955 - 5966 (2011/03/17)
Highly selective cycloisomerization of o-alkynylnitrobenzenes, leading to isatogens, has been achieved by employment of a PdII complex. This reaction is very general and functional-group-tolerant. The possible mechanism of this reaction was inv
AuBr3-catalyzed cyclization of o-(alkynyl)nitrobenzenes. Efficient synthesis of isatogens and anthranils
Asao, Naoki,Sato, Kenichiro,Yamamoto, Yoshinori
, p. 5675 - 5677 (2007/10/03)
The cyclization of o-(arylalkynyl)nitrobenzenes was catalyzed by AuBr3 to produce the corresponding isatogens in good to high yields together with small amounts of anthranils. On the other hand, anthranils were obtained selectively when the AuB
