4966-90-9 Usage
Uses
Used in Pharmaceutical Industry:
4-Hydroxy-6-methyl-3-nitro-2-pyridone is used as a reactant for the synthesis of pyridylthiazole derivatives. These derivatives are important in the development of new pharmaceutical compounds, particularly those with potential applications in the treatment of various diseases and conditions.
Used in Chemical Synthesis:
In the field of chemical synthesis, 4-hydroxy-6-methyl-3-nitro-2-pyridone serves as a key reactant for the production of 4-chloro-6-methyl-3-nitro-2-pyridone. 4-HYDROXY-6-METHYL-3-NITRO-2-PYRIDONE is further utilized in the creation of other chemical products, contributing to the diversity and innovation in the chemical industry.
Overall, 4-hydroxy-6-methyl-3-nitro-2-pyridone plays a significant role in both the pharmaceutical and chemical synthesis industries, showcasing its versatility and importance as a reactant in the development of new compounds and products.
Check Digit Verification of cas no
The CAS Registry Mumber 4966-90-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,6 and 6 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4966-90:
(6*4)+(5*9)+(4*6)+(3*6)+(2*9)+(1*0)=129
129 % 10 = 9
So 4966-90-9 is a valid CAS Registry Number.
InChI:InChI=1/C6H6N2O4/c1-3-2-4(9)5(8(11)12)6(10)7-3/h2H,1H3,(H2,7,9,10)
4966-90-9Relevant articles and documents
CRF receptor antagonists and methods relating thereto
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Page column 16, (2010/01/30)
Compounds are disclosed which have utility in the treatment of a variety of disorders, including the treatment of disorders manifesting hypersecretion of CRF in a warm-blooded animals, including stroke. The compounds of this invention have the following structures: wherein n, m, R, R1, R2, X and Ar are as defined herein, including stereoisomes and pharmaceutically acceptable salts thereof.
Thermal cyclization of 4-azido-3-nitropyridines to furoxanes [1]
Stadlbauer,Fiala,Fischer,Hojas
, p. 1253 - 1256 (2007/10/03)
4-Chloro-3-nitro-2-pyridines 3 and 10, obtained from 4-hydroxy-2-pyridones 1 and 8 after nitration and chlorination, gave with sodium azide 4-azido-3-nitropyridines 4 and 11, which cyclized on thermolysis to furoxans 6 and 12. Desoxygenation of the furoxa