1443-23-8 Usage
Uses
Used in Pharmaceutical Applications:
2,4,8,10-tetramethylpyrido[2',3':3,4]pyrazolo[1,5-a]pyrimidine is used as a potential pharmaceutical compound for its possible biological activities. Its unique structure may contribute to its potential as a therapeutic agent, warranting further research into its properties and interactions with biological systems.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, 2,4,8,10-tetramethylpyrido[2',3':3,4]pyrazolo[1,5-a]pyrimidine is used as a subject of study to understand its potential as a lead compound for drug development. Its structural features may offer insights into the design of new molecules with therapeutic potential.
Used in Chemical Synthesis and Characterization:
2,4,8,10-tetramethylpyrido[2',3':3,4]pyrazolo[1,5-a]pyrimidine is used as a challenging compound for the development of new synthetic methods and characterization techniques. Its complex structure provides an opportunity for chemists to explore innovative approaches in the synthesis and analysis of heterocyclic organic molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 1443-23-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,4 and 3 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1443-23:
(6*1)+(5*4)+(4*4)+(3*3)+(2*2)+(1*3)=58
58 % 10 = 8
So 1443-23-8 is a valid CAS Registry Number.
1443-23-8Relevant academic research and scientific papers
Keshk, Reda Mohammed
, p. 3384 - 3393 (2020)
Reaction of 3-cyano-4,6-dimethyl-2-pyridone with ethyl chloroacetate afforded ethyl 2-([3-cyano-4,6-dimethylpyridin-2-yl]oxy)acetate 2 and ethyl 2-(3-cyano-4,6-dimethyl-2-oxopyridin-1[2H]-yl)acetate 3, the reaction product yield depend on the reaction condition (potassium carbonate concentration and reaction time). These compounds used as precursors to synthesize pyridine derivatives 4, 6-10, 15, 17-20, furopyridines 5, 16, pyrazolopyridine 12, pyridopyrazolopyrimidines 14a,b. The structure of the newly synthesized compounds was confirmed by spectral data (IR, NMR, and mass spectra) and elemental analysis.
