79055-55-3 Usage
Uses
Used in Pharmaceutical Industry:
2-bromo-3-methyl-4-nitroPyridine is used as a key intermediate in the development of new drugs due to its unique functional groups that can be further modified to create therapeutically relevant molecules.
Used in Agrochemicals:
In the agrochemical industry, 2-bromo-3-methyl-4-nitroPyridine serves as a precursor in the synthesis of herbicides and insecticides, contributing to the development of effective crop protection agents.
Used in Materials Science:
2-bromo-3-methyl-4-nitroPyridine is utilized in the production of specialty chemicals and materials, where its functional groups can be exploited to create novel materials with specific properties for various applications.
Overall, 2-bromo-3-methyl-4-nitroPyridine is a multifaceted compound with a broad spectrum of uses across different industries, highlighting its importance in the synthesis of a wide range of products.
Check Digit Verification of cas no
The CAS Registry Mumber 79055-55-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,0,5 and 5 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 79055-55:
(7*7)+(6*9)+(5*0)+(4*5)+(3*5)+(2*5)+(1*5)=153
153 % 10 = 3
So 79055-55-3 is a valid CAS Registry Number.
79055-55-3Relevant academic research and scientific papers
A Journey through Hemetsberger–Knittel, Leimgruber–Batcho and Bartoli Reactions: Access to Several Hydroxy 5- and 6-Azaindoles
Radix, Sylvie,Hallé, Fran?ois,Mahiout, Zahia,Teissonnière, Amélie,Bouchez, Grégoire,Auberger, Ludovic,Barret, Roland,Lomberget, Thierry
, (2022/02/22)
The preparation of various 5- and 6-azaindoles, heterocyclic structures that are frequently part of molecules in clinical development, and their monohydroxy analogues were described. Different strategies, relying on the de novo pyrrole ring formation, were investigated and, thanks to Hemetsberger–Knittel, Bartoli and Leimgruber–Batcho approaches, 4- and 7-monohydroxy 5- and 6-azaindoles were obtained. The crucial introduction of the oxygen atom was carried out from halogen derivatives, using nucleophilic substitution reactions under basic conditions with or without a copper catalyst. Some preliminary oxidation reactions have shown that it was yet not possible to synthesize the azaquinone indole structure from monohydroxy azaindole, using molecular oxygen in the presence of salcomine as a catalyst.
