4 Bromo 1 Methyl 2 Nitro Imidazole
quinoline thiophene imidazole thiazole

4-bromo-1-methyl-2-nitro-imidazole

    Specifications

    HS Code

    277948

    Name 4-bromo-1-methyl-2-nitro-imidazole
    Molecular Formula C4H4BrN3O2
    Molecular Weight 205.99 g/mol
    Appearance Solid (Typical description, actual may vary)
    Solubility In Water Low (expected due to non - polar nature of imidazole ring and presence of hydrophobic groups)
    Solubility In Organic Solvents Soluble in common organic solvents like ethanol, acetone (due to its organic nature)

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    General Information
    Where to Buy 4-bromo-1-methyl-2-nitro-imidazole in China?
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    Frequently Asked Questions

    As a leading 4-bromo-1-methyl-2-nitro-imidazole supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

    What are the chemical properties of 4-bromo-1-methyl-2-nitro-imidazole?
    4-Bromo-1-methyl-2-nitroimidazole is also an organic compound. Its chemical properties are unique and have a variety of characteristics.
    In this compound, bromine atoms, methyl groups, nitro groups interact with imidazole rings, resulting in specific chemical activities. Bromine atoms are active and can participate in nucleophilic substitution reactions. Because of their high electronegativity, they can make the connected carbon atoms partially positively charged, vulnerable to attack by nucleophilic reagents, and new compounds are generated by being replaced with bromine.
    Methyl has an electron-pushing effect, which can affect the electron cloud density of imidazole rings, which in turn has an effect on the stability and reactivity of compounds. It can slightly increase the electron cloud density of the imidazole ring adjacent and para-position, and guide the selectivity of the reaction check point in some reactions. The nitro group at the
    2-position is a strong electron-absorbing group, which significantly reduces the electron cloud density of the imidazole ring, makes the imidazole ring more stable, but also makes it difficult to occur electrophilic substitution reactions on the ring. At the same time, the nitro group can be reduced under suitable conditions and converted into other functional groups such as amino groups, thereby expanding the derivation pathway of compounds. The synergy effect of the above functional groups of 4-bromo-1-methyl-2-nitroimidazoline is widely used in the field of organic synthesis, and can be used as a key intermediate to create various organic molecules with biological activity or special functions.
    What are the common uses of 4-bromo-1-methyl-2-nitro-imidazole?
    4-Bromo-1-methyl-2-nitroimidazole is also an organic compound. Its common uses are many, let me tell them one by one.
    First, in the field of pharmaceutical research and development, this compound is quite valuable. Because of its unique structure, potential biological activity, or can be used as a key intermediate in drug synthesis. By chemical means, it can be fused with other compounds, or new drugs can be created to treat various diseases.
    Second, in the field of materials science, it also has its uses. Due to specific chemical properties, it may participate in the process of material modification. After rational design and reaction, the material is endowed with unique characteristics, such as enhancing the stability of the material and changing its optical properties, so as to meet the needs of different application scenarios.
    Third, in the field of organic synthetic chemistry, 4-bromo-1-methyl-2-nitroimidazole is often an important reagent. Chemists can use various organic reactions according to their structural characteristics to construct more complex organic molecular structures, expand the types and functions of organic compounds, and contribute to the development of organic synthetic chemistry.
    Fourth, in terms of scientific research and exploration, because of its special structure and properties, it can provide empirical basis for chemical theoretical research. By studying its reaction mechanism, electron cloud distribution and other characteristics, scholars can deepen their understanding of the basic theory of organic chemistry and promote the progress of chemistry.
    What is 4-bromo-1-methyl-2-nitro-imidazole synthesis method?
    To prepare 4-bromo-1-methyl-2-nitro-imidazole, follow the following method.
    First take 1-methylimidazole as the starting material, which is the key substrate. In an appropriate reaction vessel, add an appropriate amount of 1-methylimidazole, and then introduce brominating reagents. Commonly used brominating reagents such as bromine (Br ²) or N-bromosuccinimide (NBS). If bromine is used, it should be slowly added dropwise in a well-ventilated environment and at low temperature because of its strong corrosiveness and volatility. When N-bromosuccinimide is used, the reaction is relatively mild. The purpose of this step is to bromide the specific position of 1-methylimidazole. In the presence of suitable catalysts and solvents, such as carbon tetrachloride, under the action of light or initiator, the bromine atom selectively replaces the hydrogen atom at the specific position on the imidazole ring to generate 4-bromo-1-methylimidazole.
    After 4-bromo-1-methylimidazole is obtained, the nitrification reaction is continued. Place 4-bromo-1-methylimidazole in another reaction vessel and add a nitrifying agent. The commonly used nitrifying reagent is mixed acid, that is, concentrated nitric acid and concentrated sulfuric acid are mixed in a certain proportion. This mixed acid has strong oxidizing and nitrifying ability. Under low temperature and strict temperature control, the mixed acid is slowly added dropwise to the system containing 4-bromo-1-methylimidazole. Concentrated sulfuric acid is not only a dehydrating agent, but also helps to generate nitroyl positive ions (NO ²), which is an active species of nitrification reaction. During the reaction process, the temperature is closely monitored to prevent side reactions from occurring. After this nitrification step, 4-bromo-1-methyl-2-nitro-imidazole can be obtained. < Br >
    However, after the reaction is completed, the product often contains impurities, which need to be separated and purified. Column chromatography can be used to select an appropriate stationary phase and eluent, and separation can be achieved according to the difference in the distribution coefficients between the product and the impurities in the stationary phase and the eluent. Recrystallization can also be used to select an appropriate solvent to dissolve the product in a hot solvent, crystallize and precipitate after cooling, and the impurities remain in the mother liquor to obtain pure 4-bromo-1-methyl-2-nitro-imidazole.
    What is the price range of 4-bromo-1-methyl-2-nitro-imidazole in the market?
    4-Bromo-1-methyl-2-nitroimidazole is in the market, what is the price? This is a fine chemical, used in medicine, pesticide synthesis and other fields. However, its market price varies depending on purity, supply and demand, and manufacturers.
    Looking at past transactions, if the purity is ordinary, it is about ten yuan per gram. However, if the purity is high, the price may increase several times. If the purchase volume is large, the manufacturer may make a profit to reduce the unit price.
    When the market demand exceeds the supply, the price will rise; if the supply exceeds the demand, the price will drop. And different manufacturers have different pricing due to cost differences. Large manufacturers produce standard, the cost may be high, and the price is also high; small manufacturers may have lower prices due to low costs.
    To know the exact price, you must consult chemical raw material suppliers, chemical reagent companies, or check on the chemical trading platform to get the current market.
    What are the manufacturers of 4-bromo-1-methyl-2-nitro-imidazole?
    4-Bromo-1-methyl-2-nitroimidazole, in today's chemical industry, there are various manufacturers involved in its production. However, I have read the classics, but I have not seen a detailed list of the names of these manufacturers.
    Looking at the current chemical industry landscape, there are many manufacturers specializing in the production of heterocyclic compounds, or involved in the industry of 4-bromo-1-methyl-2-nitroimidazole. Gain heterocyclic compounds are widely used in medicine, pesticides, materials and other fields. Such manufacturers often develop and produce various heterocyclic compounds in response to market needs, 4-bromo-1-methyl-2-nitroimidazole or among them.
    Some factories focus on the manufacture of fine chemicals. The production of fine chemicals is known for its fine process and strict quality requirements. 4-bromo-1-methyl-2-nitroimidazole may be one of its product lines. With their exquisite craftsmanship and advanced equipment, they are committed to producing high-quality fine chemicals, 4-bromo-1-methyl-2-nitroimidazole may also be their key products.
    If you want to know the manufacturer who actually produces this product, you need to consult the chemical directory, industry report, or consult the industry veteran. And the chemical industry is unpredictable, the rise and fall of manufacturers and the improvement of products happen from time to time. Therefore, if you want to obtain accurate and up-to-date information, you can only obtain it when you continue to pay attention to industry trends and search for information widely.