885272-41-3 Usage
Uses
Used in Pharmaceutical Research:
5-THIOPHEN-3-YL-1H-INDAZOLE is used as a potential drug candidate for its anti-cancer, anti-inflammatory, and antimicrobial properties. It is valued for its ability to target various biological pathways and mechanisms, making it a promising agent for the development of new therapeutics.
Used in Cancer Treatment:
In the field of oncology, 5-THIOPHEN-3-YL-1H-INDAZOLE is used as an anti-cancer agent, targeting different types of cancer cells and potentially contributing to the inhibition of tumor growth and progression.
Used in Inflammation Management:
5-THIOPHEN-3-YL-1H-INDAZOLE is utilized as an anti-inflammatory agent, which may help in the treatment of various inflammatory conditions by modulating the body's inflammatory response.
Used in Antimicrobial Therapy:
5-THIOPHEN-3-YL-1H-INDAZOLE is also used in antimicrobial applications, where it can potentially combat a range of microbial infections, including bacterial and fungal diseases.
Used in Biological Imaging:
5-THIOPHEN-3-YL-1H-INDAZOLE has been investigated for its potential as a fluorescent dye in biological imaging, which could enhance the visualization of cellular and molecular processes in research and diagnostic settings.
Check Digit Verification of cas no
The CAS Registry Mumber 885272-41-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,5,2,7 and 2 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 885272-41:
(8*8)+(7*8)+(6*5)+(5*2)+(4*7)+(3*2)+(2*4)+(1*1)=203
203 % 10 = 3
So 885272-41-3 is a valid CAS Registry Number.
885272-41-3Relevant academic research and scientific papers
Oh, Yoo Jin,Yum, Eul Kgun
, p. 404 - 411 (2019)
Diverse mono or biaryl substituents were introduced to indazole moieties under microwave-assisted palladium-catalyzed coupling reactions with isomeric bromoindazoles and aryl boronic acids. 1,3-Disubstituted indazoles were also obtained by C?C or C?N coupling of monosubstituted indazoles with functionalized terminal alkenes and arylhalides. Facile introduction of diverse substituents to indazoles showed useful synthetic approach for creating indazole compound library to discover biologically active small molecules.
