80840-19-3 Usage
Uses
Used in Organic Synthesis:
(6-methylpyridin-2-yl)cyanamide is used as a building block in organic synthesis for the creation of various complex organic molecules. Its unique structure allows for the formation of diverse chemical entities, making it a valuable component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Development:
In the pharmaceutical industry, (6-methylpyridin-2-yl)cyanamide is used as a starting material for the development of new drugs. Its potential biological activity and versatile chemical structure make it a promising candidate for the design and synthesis of novel therapeutic agents.
Used in Agrochemical Research:
(6-methylpyridin-2-yl)cyanamide is also utilized in agrochemical research for the development of new pesticides and other agricultural chemicals. Its unique properties and potential for chemical modification make it a valuable tool in the search for more effective and environmentally friendly agrochemicals.
Used in Medicinal Chemistry:
Due to its potential biological activity, (6-methylpyridin-2-yl)cyanamide is of interest for further study in medicinal chemistry. Researchers may explore its interactions with biological targets and evaluate its potential as a therapeutic agent or as a lead compound for the development of new drugs.
Check Digit Verification of cas no
The CAS Registry Mumber 80840-19-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,8,4 and 0 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 80840-19:
(7*8)+(6*0)+(5*8)+(4*4)+(3*0)+(2*1)+(1*9)=123
123 % 10 = 3
So 80840-19-3 is a valid CAS Registry Number.
80840-19-3Relevant academic research and scientific papers
Bell, Harold M.,Carver, David R.,Hubbard, James S.,Sachdeva, Yesh P.,Wolfe, James F.,Greenwood, Thomas D.
, p. 3442 - 3444 (1985)
Treatment of 2,4-dichloropyrimidine (1) with a series of ketone potassium enolate in liquid NH3 results in a novel ring transformation leading to the formation of 6-(cyanamino)pyridines (8a-c).An SN(ANRORC) mechanism initiated by nucleophilic addition of the enolate to C6 of 1 is proposed.The pyrimidine-pyridine transformation involves displacement of the N1-C2-N3 portion of pyrimidine with a C-C-N moiety, where the enolate contributes the C-C fragment while NH3 is shown, using 15N-labeled NH3, to be the N donor.
