766515-45-1 Usage
Molecular Structure
1-methyl-3-iodo-5-phenylethynyl-1H-pyrazolo[3,4-b]pyridine has a complex molecular structure that belongs to the pyrazolo[3,4-b]pyridine family.
Functional Groups
The compound contains a methyl group (-CH3), an iodine atom (I), and a phenylethynyl group (C6H5-C≡C-).
Chemical Properties
Due to its unique chemical properties, it is commonly used in organic synthesis and pharmaceutical research.
Potential Applications
The compound may have potential applications in drug discovery and development, particularly in the field of neurological disorders and cancer research.
Handling Precautions
It is important to handle 1-methyl-3-iodo-5-phenylethynyl-1H-pyrazolo[3,4-b]pyridine with caution due to its potential reactivity and toxicity.
Further Research
Additional research and testing are necessary to fully understand the compound's potential uses and risks.
Check Digit Verification of cas no
The CAS Registry Mumber 766515-45-1 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, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 766515-45:
(8*7)+(7*6)+(6*6)+(5*5)+(4*1)+(3*5)+(2*4)+(1*5)=191
191 % 10 = 1
So 766515-45-1 is a valid CAS Registry Number.
766515-45-1Relevant articles and documents
Synthesis of 3,5-difunctionalized 1-methyl-1H-pyrazolo[3,4-b]pyridines involving palladium-mediated coupling reactions
Lavecchia,Berteina-Raboin,Guillaumet
, p. 6633 - 6636 (2007/10/03)
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.
