76006-09-2 Usage
Uses
Used in Pharmaceutical Industry:
1,6-DIHYDRO-7H-PYRAZOLO[3,4-C]PYRIDIN-7-ONE is used as a research compound for its potential role in modulating the central nervous system. It is being studied for its ability to inhibit the enzyme cGMP-specific phosphodiesterase, which may have implications for the treatment of neurological disorders and other medical conditions.
Used in Neuroscience Research:
In the field of neuroscience, 1,6-DIHYDRO-7H-PYRAZOLO[3,4-C]PYRIDIN-7-ONE is used as a tool to investigate the mechanisms of the central nervous system. Its capacity to interact with specific enzymes and pathways could provide insights into the development of new therapeutic approaches for neurological conditions.
Used in Neuropharmacology:
1,6-DIHYDRO-7H-PYRAZOLO[3,4-C]PYRIDIN-7-ONE serves as a compound of interest in neuropharmacology, where it is being examined for its potential to influence neural signaling and neurotransmission. Understanding its effects could contribute to the advancement of treatments for various neurological disorders.
Check Digit Verification of cas no
The CAS Registry Mumber 76006-09-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,0,0 and 6 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 76006-09:
(7*7)+(6*6)+(5*0)+(4*0)+(3*6)+(2*0)+(1*9)=112
112 % 10 = 2
So 76006-09-2 is a valid CAS Registry Number.
76006-09-2Relevant academic research and scientific papers
Pyrazolopyridines. Part 5. Preparation and Reactions of Pyrazolopyridines
Chapman, David,Hurst, Jim
, p. 2398 - 2404 (2007/10/02)
A series of pyrazolopyridines has been prepared by nitrosation of 3-acetamido-4-methylpyridines and subsequent rearrangement and cyclisation of the N-acetyl-N-nitroso-compounds produced.The reactions of the pyrazolopyridines have been investigated. 1- and 2-Acetyl and 1- and 2-benzyl compounds were obtained and their structures elucidated spectroscopically.The ring system readily undergoes electrophilic substitution in the 3-position. 7-Chloropyrazolopyridine has been shown to be more susceptible to nucleophilic substitution than the isomeric 5-chloro-compound.
