2 Methyl 4 5 Iodoimidazole
quinoline thiophene imidazole thiazole

2-methyl-4(5)-iodoimidazole

    Specifications

    HS Code

    917978

    Name 2-methyl-4(5)-iodoimidazole
    Chemical Formula C4H5IN2
    Molar Mass 209.998 g/mol
    Appearance Solid (likely, typical for many imidazole derivatives)
    Solubility In Water Limited solubility, imidazole derivatives generally have low solubility in water
    Solubility In Organic Solvents Soluble in some organic solvents like ethanol, acetone (common for such organic compounds)
    Stability Stable under normal conditions, but may react with strong oxidizing agents

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    General Information
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    Frequently Asked Questions

    As a leading 2-methyl-4(5)-iodoimidazole 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 main uses of 2-methyl-4 (5) -iodoimidazole?
    2-Methyl-4 (5) -iodoimidazole is one of the organic compounds. Its main uses are important in the fields of medicinal chemistry and organic synthesis.
    In medicinal chemistry, this compound is often the key intermediate for the creation of new drugs. Due to its unique chemical structure, it can interact with specific targets in organisms or be transformed through specific chemical reactions to obtain therapeutic drug components. For example, the synthesis of some antibacterial and antiviral drugs often relies on this compound as a starting material. By means of organic synthesis, its structure is added or modified to make it have the ability to target specific pathogens, so as to exert the effect of treating diseases.
    In the field of organic synthesis, 2-methyl-4 (5) -iodoimidazole is also an indispensable reagent. Due to the existence of iodine atoms and imidazole rings, it is endowed with active chemical properties and can participate in many classic organic reactions, such as nucleophilic substitution reactions, coupling reactions, etc. In nucleophilic substitution reactions, iodine atoms are easily replaced by nucleophilic reagents, thereby introducing different functional groups and expanding the structural diversity of molecules. In coupling reactions, it can be coupled with other organic halides or unsaturated compounds to construct more complex organic molecular structures, providing key intermediates for the synthesis of new materials and the total synthesis of natural products.
    In summary, 2-methyl-4 (5) -iodoimidazole plays an important role in the field of medicine and organic synthesis due to its special structure and chemical activity, and promotes the development of new drugs and the creation of organic compounds.
    What are the physical properties of 2-methyl-4 (5) -iodoimidazole?
    2-Methyl-4 (5) -iodoimidazole is one of the organic compounds. Its physical properties are quite important and have an impact in chemical, pharmaceutical and other fields.
    First of all, its appearance, under normal conditions, or in a white to light yellow crystalline powder shape, this appearance is conducive to observation and preliminary identification. Looking at it, the texture is delicate, like fine grains gathered in one place, or shimmering under light, like fine pearls.
    When it comes to melting point, it is within a certain temperature range. This property is of great significance for material identification and purification processes. Just like a precise scale, it can help identify authenticity and purity. When heated to this specific temperature, its solid lattice structure gradually disintegrates, and the molecules are energized and agile. The process is smooth and characteristic.
    Solubility is also key. In common organic solvents, such as ethanol and dichloromethane, it has a certain solubility. Ethanol is as agile as water, interacting with the molecules of the compound, and some molecules break free from each other and disperse in the ethanol medium, just like fish swimming in water. However, in water, the solubility is poor. Due to its weak affinity between molecular structure and water molecules, the two are difficult to blend. Just like oil and water, they are distinct.
    In addition, the density of the compound is also a specific value. This value reflects the degree of molecular compactness, which is related to its sedimentation and delamination in the mixture. Like an object in a fluid, the density difference determines its floating state, which is of great significance to the separation step of chemical operations.
    Because of its structure containing iodine atoms and imidazole rings, it has certain stability and can participate in chemical reactions under specific conditions. This chemical activity is related to physical properties and jointly determines its performance in practical applications.
    What is the chemical synthesis method of 2-methyl-4 (5) -iodoimidazole?
    The chemical synthesis of 2-methyl-4 (5) -iodoimidazole is a very important topic. This synthesis method is often obtained from a specific starting material through several delicate reactions.
    At the beginning, compounds with specific structures are often selected, such as precursors containing imidazole rings. This precursor needs to have appropriate substituents for subsequent iodine substitution and methylation reactions.
    The iodine substitution reaction is one of the key steps. Often use a suitable iodine substitution reagent, such as iodine elemental substance ($I_2 $) with a specific oxidizing agent, or use an iodine-containing organic reagent. Under suitable reaction conditions, such as specific temperature and solvent environment, the iodine generation occurs at a specific position of the imidazole ring. This process needs to be carefully regulated, and the iodine generation position and yield will be significantly affected due to differences in reaction conditions.
    Methylation is also indispensable. Methylation reagents such as iodomethane ($CH_3I $) or dimethyl sulfate ($ (CH_3) _2SO_4 $) are often used. In an alkaline environment or in the presence of a specific catalyst, specific atoms on the imidazole ring are connected to methyl groups to form 2-methyl-4 (5) -iodoimidazole. During the
    reaction process, temperature control is extremely important. If the temperature is too low, the reaction rate is slow and takes a long time; if the temperature is too high, it may cause side reactions and reduce the purity of the product. The choice of solvent also has a great influence, and different solvents have different solubility and reactivity of the reactants. It is necessary to choose the appropriate one.
    After the reaction is completed, it needs to be separated and purified. Commonly used methods include column chromatography, recrystallization, etc., to obtain high-purity 2-methyl-4 (5) -iodoimidazole. In this way, the target product can be obtained through carefully designed reaction steps, precisely controlled reaction conditions, and meticulous separation and purification.
    What is the price range of 2-methyl-4 (5) -iodoimidazole in the market?
    What you are asking is the price range of 2-methyl-4 (5) -iodoimidazole in the market. However, the price of this chemical substance varies for many reasons.
    First, purity is the key. If the purity is high, the price of a nearly perfect pure product will be high; if it contains impurities, although the price can be reduced, it will also affect the use.
    Second, the trend of supply and demand also affects its price. If there are many people in the market and there are few suppliers, the price will rise; if the supply exceeds the demand, the price will drop.
    Third, the method and cost of making this product are also important factors. If the production method is complicated and rare reagents are required, the cost will be high, and the price will follow.
    Fourth, the difference between sellers also makes the price different. Well-known merchants, because of their reputation, the price may be high; small merchants compete for the market, and the price may be slightly lower.
    The price of 2-methyl-4 (5) -iodine imidazole in the market today ranges from tens to hundreds of yuan per gram. However, this is only a rough figure. The actual price still needs to be consulted with chemical reagent merchants. According to the current situation, the exact number can be obtained.
    What are the storage conditions for 2-methyl-4 (5) -iodoimidazole?
    2-Methyl-4 (5) -iodoimidazole is also an organic compound. Its preservation conditions are concerned with the quality and use of this substance.
    Cover these compounds, they are more active and easily disturbed by various external factors. First, when avoiding direct light. Light can promote its chemical reaction and cause structural changes, so it is better to hide in a dark room or store it in an opaque container.
    Second, temperature is also critical. Under normal temperature, or there is a slow change, so it is often necessary to place it in a low temperature to reduce the activity of its molecules. Generally speaking, the temperature of refrigeration is between two and eight degrees, which is more suitable. < Br >
    Third, in the air, oxygen and water vapor can interact with it. Oxygen can lead to oxidation, water vapor or hydrolysis. Therefore, when sealed and stored, it should be kept out of contact with the air. Airtight bottles and cans are commonly used, and desiccant may be added to them to keep the environment dry.
    Fourth, you should also pay attention to the objects you come into contact with. Do not coexist with substances that can chemically react, such as strong acids, strong bases, etc., to avoid change.
    All of these are conditions that should be paid attention to for the preservation of 2-methyl-4 (5) -imidazole. According to this, the stability of this substance can be maintained for later use.