824429-50-7 Usage
Uses
Used in Medicinal Chemistry and Drug Development:
N-(6-HYDROXY-PYRIDIN-2-YL)-2,2-DIMETHYL-PROPIONAMIDE is used as a building block for the synthesis of potential pharmaceutical agents due to its unique structural features and reactivity in chemical reactions.
Used in Biological Research:
N-(6-HYDROXY-PYRIDIN-2-YL)-2,2-DIMETHYL-PROPIONAMIDE is used as a compound with potential biological activities, such as anti-inflammatory and antioxidant properties, for the development of new therapeutic agents.
Used in Coordination Chemistry:
N-(6-HYDROXY-PYRIDIN-2-YL)-2,2-DIMETHYL-PROPIONAMIDE is used as a ligand in coordination chemistry, where it can form complexes with metal ions, potentially leading to new materials with specific applications in various fields.
Used in Chemical Reactions:
Due to its reactivity and structural properties, N-(6-HYDROXY-PYRIDIN-2-YL)-2,2-DIMETHYL-PROPIONAMIDE is used in various chemical reactions to synthesize a range of compounds for different applications in the chemical and pharmaceutical industries.
Check Digit Verification of cas no
The CAS Registry Mumber 824429-50-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,2,4,4,2 and 9 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 824429-50:
(8*8)+(7*2)+(6*4)+(5*4)+(4*2)+(3*9)+(2*5)+(1*0)=167
167 % 10 = 7
So 824429-50-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H14N2O2/c1-10(2,3)9(14)12-7-5-4-6-8(13)11-7/h4-6H,1-3H3,(H2,11,12,13,14)
824429-50-7Relevant academic research and scientific papers
O?mia?owski, Borys,Kolehmainen, Erkki,Ikonen, Satu,Ahonen, Kari,L?fman, Miika
, p. 678 - 683 (2011)
2-Acylamino-6-[1H]-pyridones [acyl = RCO, where R = methyl (1), ethyl (2), iso-propyl (3), tert-butyl (4), and 1-adamantyl (5)] have been synthesized and characterized by NMR spectroscopy. From three congeners, 2, 3 and 5, also single crystal X-ray structures have been solved. For these derivatives GIPAW calculations acts as a "bridge" between solid-state NMR data and calculated chemical shifts based on X-ray determined geometry. In crystals all three compounds exist as pyridone tautomers possessing similar six-membered ring structure stabilized by intramolecular CO?HN hydrogen bond. Theoretical GIPAW calculated and experimental 13C and 15N CPMAS NMR shifts are in excellent agreement with each other.
