60323-95-7 Usage
Uses
Used in Pharmaceutical Industry:
2-Chloro-3-methyl-4-nitropyridine 1-oxide is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique chemical structure allows it to be a building block for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, 2-Chloro-3-methyl-4-nitropyridine 1-oxide serves as an essential intermediate for the production of pesticides and other agrochemicals. Its incorporation into these products can enhance their effectiveness in controlling pests and diseases in agriculture.
Used in Organic Synthesis:
2-Chloro-3-methyl-4-nitropyridine 1-oxide is also utilized in the synthesis of other organic compounds. Its versatile chemical properties make it a valuable precursor for the creation of a wide range of organic molecules with various applications in different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 60323-95-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,3,2 and 3 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 60323-95:
(7*6)+(6*0)+(5*3)+(4*2)+(3*3)+(2*9)+(1*5)=97
97 % 10 = 7
So 60323-95-7 is a valid CAS Registry Number.
60323-95-7Relevant 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.
