Nombre del producto:2-bromo-4-nitro-1H-imidazole

IUPAC Name:2-bromo-4-nitro-1H-imidazole

CAS:65902-59-2
Fórmula molecular:C3H2BrN3O2
Pureza:95%+
Número de catálogo:CM101985
Peso molecular:191.97

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CM101985-25g in stock NJũ
CM101985-100g in stock ǜȺȬ

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Detalles del producto

Núm. De CAS :65902-59-2
Fórmula molecular:C3H2BrN3O2
Punto de fusión:-
Código de sonrisas:O=[N+](C1=CNC(Br)=N1)[O-]
Densidad:2.156 g/cm3
Número de catálogo:CM101985
Peso molecular:191.97
Punto de ebullición:402.5°C at 760 mmHg
Nº Mdl:MFCD09038915
Almacenamiento:Keep in a tight container and store at ambient temperature

Category Infos

Imidazoles
Imidazole is an important five-membered nitrogen-containing heterocyclic compound. Among the numerous heterocyclic compounds, imidazole and its derivatives are regarded as a unique and multifaceted scaffold material due to their diverse applications in industrial, organic and pharmaceutical chemistry. Imidazoles interact in different ways with many therapeutic targets, enzymes and receptors in biological systems and thus exhibit a wide range of biological activities. In particular, several imidazoles can be used as clinical drugs to treat various types of cancer with high therapeutic efficacy. Furthermore, imidazoles are one of the most critical segments in the field of anti-covid-19 virus drug discovery due to their ability to interact with active targets in living systems.
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Product Other Information

Product Overview 2-bromo-4-nitro-1H-imidazole (BNI) is an organic compound that has been used in various scientific research applications. BNI is a versatile and useful reagent in organic synthesis, and has been used to synthesize a variety of compounds, including pharmaceuticals, agrochemicals, and dyes. BNI is also used in many biochemical and physiological studies, as it can act as a substrate and inhibitor in various biochemical pathways.
Synthesis and Application 2-bromo-4-nitro-1H-imidazole can be synthesized in a variety of ways, depending on the desired purity and quantity. One of the most common methods for synthesizing 2-bromo-4-nitro-1H-imidazole is the nitration of 2-bromo-4-methyl-1H-imidazole. This reaction involves the reaction of 2-bromo-4-methyl-1H-imidazole with nitric acid and sulfuric acid, which produces a mixture of 2-bromo-4-nitro-1H-imidazole and 2-bromo-4-nitro-2H-imidazole. This mixture can then be separated by column chromatography. Another method for synthesizing 2-bromo-4-nitro-1H-imidazole involves the reaction of 2-bromo-4-methyl-1H-imidazole with sodium nitrite in the presence of acetic acid. This reaction produces a mixture of 2-bromo-4-nitro-1H-imidazole and 2-bromo-4-nitro-2H-imidazole, which can then be separated by column chromatography. 2-Bromo-4-nitro-1H-imidazole has been used in a variety of scientific research applications. It has been used as a substrate and inhibitor in various biochemical pathways, and as an intermediate in the synthesis of various compounds. 2-bromo-4-nitro-1H-imidazole has also been used as a catalyst in organic synthesis, and as a reagent for the detection and quantification of various molecules. Additionally, 2-bromo-4-nitro-1H-imidazole has been used in the study of the structure and function of enzymes, and in the study of the mechanisms of drug action.
Future Directions 2-bromo-4-nitro-1H-imidazole has a variety of potential future directions. 2-bromo-4-nitro-1H-imidazole can be used to study the structure and function of enzymes, and to study the mechanisms of drug action. Additionally, 2-bromo-4-nitro-1H-imidazole can be used to develop new drugs and agrochemicals, as well as to study the biochemical and physiological effects of various compounds. 2-bromo-4-nitro-1H-imidazole can also be used in the development of new analytical techniques, and in the study of the mechanisms of drug resistance. Finally, 2-bromo-4-nitro-1H-imidazole can be used in the synthesis of new compounds, and in the study of the structure and function of proteins.