137225-08-2 Usage
Uses
Used in Pharmaceutical Industry:
2-[(3-methoxyphenyl)amino]isonicotinonitrile is used as a potential drug candidate for its antitumor and antiviral activities. It has been studied for its ability to target and treat various diseases, particularly those related to cancer and viral infections, due to its unique chemical structure and biological activity.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, 2-[(3-methoxyphenyl)amino]isonicotinonitrile serves as a valuable building block for the development of new chemical compounds with potential therapeutic applications. Its structural features allow for the design and synthesis of novel molecules that can be further optimized for specific medical uses.
Used in Organic Synthesis:
2-[(3-methoxyphenyl)amino]isonicotinonitrile is also utilized in organic synthesis as a key intermediate for the preparation of other complex organic molecules. Its reactivity and functional groups make it a versatile component in the synthesis of a wide range of chemical products, including pharmaceuticals, agrochemicals, and other specialty chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 137225-08-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,2,2 and 5 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 137225-08:
(8*1)+(7*3)+(6*7)+(5*2)+(4*2)+(3*5)+(2*0)+(1*8)=112
112 % 10 = 2
So 137225-08-2 is a valid CAS Registry Number.
137225-08-2Relevant academic research and scientific papers
Photochemically Induced Electron Transfer from Aniline Derivatives to Pyridine-2,4-dicarbonitrile: Synthetic and Mechanistic Aspects
Bernardi, Rosanna,Caronna, Tullio,Morrocchi, Sergio,Vittimberga, Bruno M.
, p. 1411 - 1415 (2007/10/02)
A study on the photochemically induced electron transfer from substituted aniline donors to a 2,4-dicyanopyridine acceptor permits the synthesis of new amino derivatives of the pyridine and forms the basis of a hypothesis on the mechanism of the reaction and the influence of the substituent on the aniline ring.
