33245-30-6 Usage
Uses
Used in Organic Synthesis:
Hydroxy-[(4-methylpyridin-2-yl)amino]-oxo-azanium is utilized as a reagent in organic synthesis for its ability to participate in various chemical reactions. Its reactive groups, such as the hydroxy and amino groups, facilitate the formation of new chemical bonds and the synthesis of complex organic molecules.
Used in Pharmaceutical Research:
In the pharmaceutical industry, hydroxy-[(4-methylpyridin-2-yl)amino]-oxo-azanium serves as a valuable compound for research purposes. Its potential biological activity and pharmacological properties make it a promising candidate for the development of new drugs. Researchers can explore its interactions with biological targets and evaluate its efficacy in treating various diseases.
Used as a Precursor in Chemical Entities:
Hydroxy-[(4-methylpyridin-2-yl)amino]-oxo-azanium can also be employed as a precursor to other chemical entities. Its structural properties and reactive groups allow for further modification and functionalization, leading to the creation of new compounds with specific applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 33245-30-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,2,4 and 5 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 33245-30:
(7*3)+(6*3)+(5*2)+(4*4)+(3*5)+(2*3)+(1*0)=86
86 % 10 = 6
So 33245-30-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H8N3O2/c1-5-2-3-7-6(4-5)8-9(10)11/h2-4H,1H3,(H,7,8)(H,10,11)/q+1
33245-30-6Relevant academic research and scientific papers
Method of preparation of nitroaminopyridine compounds
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Page/Page column 2, (2008/06/13)
A method of preparing an intermediate which is useful for the preparation of azaindole derivatives.
An alternate route to 2-amino-3-nitro-5-bromo-4-picoline: Regioselective pyridine synthesis via 2-nitramino-picoline intermediate
Bhattacharya, Apurba,Purohit, Vikram C.,Deshpande, Prashant,Pullockaran, Annie,Grosso, John A.,DiMarco, John D.,Gougoutas, Jack Z.
, p. 885 - 888 (2012/12/30)
The 2-nitramino functionality in 2-nitramino-4-picoline was successfully exploited not only as a protecting group but also as a directional handle to afford an efficient, atom-economic, and regioselective synthesis of 2-amino-5-bromo-3-nitro-4-picoline (4), a precursor for a drug candidate in development.
Substituent Effects on the Isomer Ratios in the Rearrangement of Some 2- and 4-Nitraminopyridines
Deady, Leslie W.,Korytsky, Olga L.,Rowe, Jeffrey E.
, p. 2025 - 2034 (2007/10/02)
The preparation, and rearrangement in 92percent sulfuric acid, of 4-X-2-nitramino- (1), 2-X-4-nitramino- (2), and 6-X-2-nitramino-pyridines (3) is reported (X=H,Me,MeO,Br,Cl,CO2H).The product isomer ratios can be explained by differential electronic stabilization of the appropriate ? complexes for aromatic nitration and steric effects seem relatively unimportant.Deuteration had no effect on the product distribution
