766515-35-9 Usage
Uses
Used in Pharmaceutical Research:
5-IODO-1-METHYL-1H-PYRAZOLO[3,4-B] PYRIDIN-3-AMINE is used as a research compound for the development and testing of pharmaceuticals. Its unique structure and properties make it a valuable tool in the discovery of new drug candidates and the understanding of their mechanisms of action.
Used in Chemical Synthesis:
In the chemical industry, 5-IODO-1-METHYL-1H-PYRAZOLO[3,4-B] PYRIDIN-3-AMINE is used as an intermediate in the synthesis of more complex molecules. Its nitrogen-rich heterocyclic ring structure and iodine substituent provide opportunities for further chemical reactions and modifications, leading to the creation of novel compounds with potential applications in various fields.
Used in Academic Research:
5-IODO-1-METHYL-1H-PYRAZOLO[3,4-B] PYRIDIN-3-AMINE is used as a research material in academic institutions, where scientists and researchers explore its chemical properties, reactivity, and potential applications. 5-IODO-1-METHYL-1H-PYRAZOLO[3,4-B] PYRIDIN-3-AMINE serves as a model system for studying the behavior of similar compounds and contributes to the advancement of knowledge in the field of chemistry and related disciplines.
Check Digit Verification of cas no
The CAS Registry Mumber 766515-35-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,6,6,5,1 and 5 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 766515-35:
(8*7)+(7*6)+(6*6)+(5*5)+(4*1)+(3*5)+(2*3)+(1*5)=189
189 % 10 = 9
So 766515-35-9 is a valid CAS Registry Number.
766515-35-9Relevant academic research and scientific papers
Lavecchia,Berteina-Raboin,Guillaumet
, p. 6633 - 6636 (2004)
Indirect iodination of 2-chloro-nicotinonitrile gave 2-chloro-5- iodonicotinonitrile, which was cyclized with methylhydrazine to lead to 3-amino-5-iodopyrazolo[3,4-b]pyridine. Position 3 was then protected by pivaloyl group and the resulting 5-iodo-3-pivaloylaminopyrazolo[3,4-b]pyridine was engaged in palladium-promoted coupling reactions with various reagents to give 3-pivaloylamino-5-substituted compounds. Deprotection and iododediazoniation followed by cross-coupling reactions in position 3 afforded novel unsymmetrical 3,5-disubstituted pyrazolo[3,4-b]pyridine species.
