CAS NO:68957-50-6 5-bromo-6-methyl-3-nitropyridin-2-amine
CAS NO:68957-50-6 NAME:5-bromo-6-methyl-3-nitropyridin-2-amine MF：C6H6BrN3O2 MW：232.03 EINECS：273-342-3 PURITY:97%MIM APPEARANCE:Powder COA:AVAILABLE SYNONYMS:2-Amino-5-bromo-6-methyl-3-nitropyridine
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Material Chemistry
Other Material Chemicals
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Product introduction
| PRODUCT NAME | 5-bromo-6-methyl-3-nitropyridin-2-amine |
| CAS NO | 68957-50-6 |
| FP | 145℃ |
| BP | 316℃ |
| DENSITY | 1.795 |
| STORAGE | Keep in dark place,Inert atmosphere,Room temperature |
| DELIVERY | 2-3DAYS |
| PACKAGE | According client's request |
Description of CAS NO:68957-50-6 5-bromo-6-methyl-3-nitropyridin-2-amine
The compound "5-Bromo-6-methyl-3-nitropyridin-2-amine" is a derivative of pyridine, a heterocyclic aromatic organic compound.It has potential applications in pharmaceuticals and materials science.
Applications of CAS NO:68957-50-6 5-bromo-6-methyl-3-nitropyridin-2-amine
1)Synthetic Methodologies :in the synthesis of 5-Bromo-2-nitropyridine, highlights the importance of robust reaction conditions for the synthesis of nitropyridine derivatives. These methodologies can be crucial for producing compounds like "5-Bromo-6-methyl-3-nitropyridin-2-amine" on a large scale with high purity and reproducibility, which is vital for further applications in material science or pharmacology
2)Fluorescent Probes Development : The creation of aminoethylpyridine-based fluorescent probes for detecting metal ions in aqueous media showcases the potential of nitropyridine derivatives in sensor technology. Derivatives similar to "5-Bromo-6-methyl-3-nitropyridin-2-amine" could be designed to serve as sensitive and selective probes for environmental monitoring, biomedical diagnostics, and chemical sensing
3)Computational Insights and Drug Interaction : Computational studies on similar nitropyridine compounds, focusing on molecular structure, energy levels, and docking simulations, can guide the development of new drugs or materials. For instance, the speculative assessment and molecular docking studies of nitropyridine derivatives highlight the potential for these compounds in understanding protein interactions and designing inhibitors for specific targets, which might extend to derivatives like "5-Bromo-6-methyl-3-nitropyridin-2-amine"
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