245325-34-2 Usage
Uses
Used in Pharmaceutical Industry:
1H-Pyrazolo[3,4-c]pyridine-3-carbonitrile(9CI) is used as a building block for the synthesis of various biologically active molecules, contributing to the development of novel drugs with potential therapeutic effects.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 1H-Pyrazolo[3,4-c]pyridine-3-carbonitrile(9CI) is utilized for its role in the creation of new drug candidates, particularly those with potential applications in treating various diseases and conditions.
Used in Antimicrobial Applications:
1H-Pyrazolo[3,4-c]pyridine-3-carbonitrile(9CI) is studied for its antimicrobial properties, making it a promising candidate for the development of new antimicrobial agents to combat resistant bacterial strains.
Used in Antifungal Applications:
1H-Pyrazolo[3,4-c]pyridine-3-carbonitrile(9CI) is also recognized for its antifungal properties, indicating its potential use in the development of antifungal medications to treat fungal infections.
Used in Antiviral Applications:
1H-Pyrazolo[3,4-c]pyridine-3-carbonitrile(9CI) has been studied for its antiviral properties, suggesting its possible use in the creation of antiviral drugs to treat viral infections.
Check Digit Verification of cas no
The CAS Registry Mumber 245325-34-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,5,3,2 and 5 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 245325-34:
(8*2)+(7*4)+(6*5)+(5*3)+(4*2)+(3*5)+(2*3)+(1*4)=122
122 % 10 = 2
So 245325-34-2 is a valid CAS Registry Number.
245325-34-2Relevant academic research and scientific papers
Synthesis, reactivity and 13C-NMR of 1H-pyrazolo[3,4-c]pyridine derivatives
Milhavet, Jean-Claude,Gueiffier, Alain,Bernal, Lysiane,Teulade, Jean-Claude
, p. 1661 - 1667 (2007/10/03)
The synthesis of various 1H-pyrazolo [.-c.]pyridines was reported. 3- Cyano derivatives were obtained from the corresponding nitro compounds by Sandmeyer Reaction using Na3[Cu(CN)4] at pH 1. The 13C-NMR data of this series were also described.
