1 2 2 4 Dichlorobenzyl Oxy 2 2 4 Dichlorophenyl Ethyl 1h Imidazole Nitrate 1 1
quinoline thiophene imidazole thiazole

1-{2-[(2,4-dichlorobenzyl)oxy]-2-(2,4-dichlorophenyl)ethyl}-1H-imidazole nitrate (1:1)

    Specifications

    HS Code

    433757

    Chemical Name 1-{2-[(2,4-dichlorobenzyl)oxy]-2-(2,4-dichlorophenyl)ethyl}-1H-imidazole nitrate (1:1)
    Molecular Formula C20H16Cl4N3O4
    Molecular Weight 507.17 g/mol
    Appearance Typically a solid (description may vary)
    Solubility Solubility characteristics depend on the solvent (e.g., solubility in organic solvents to be determined by experiment)
    Melting Point Specific melting point value requires experimental determination
    Boiling Point Boiling point information requires experimental determination
    Pka Acid dissociation constant value requires experimental determination
    Logp Partition coefficient value requires experimental determination
    Vapor Pressure Vapor pressure value requires experimental determination

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    Frequently Asked Questions

    As a leading 1-{2-[(2,4-dichlorobenzyl)oxy]-2-(2,4-dichlorophenyl)ethyl}-1H-imidazole nitrate (1:1) supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

    What is the chemical structure of 1- {2- [ (2,4-dichlorobenzyl) oxy] 2- (2,4-dichlorophenyl) ethyl} -1H-imidazole nitrate (1:1)
    This is a problem of structural analysis of organic compounds. 1 - {2- [ (2,4-dichlorobenzyl) oxy] -2 - (2,4-dichlorobenzyl) ethyl} -1H-indole-3-formic anhydride (1:1), its chemical structure is quite complex.
    In terms of view, 1H-indole-3-formic anhydride is the core structure of this compound. 1H-indole is a nitrogen-containing heterocyclic aromatic hydrocarbon, and its 3-position is connected to the structure of formic anhydride.
    Looking at the side chain, in the group at the first position, there is a long chain structure. The long chain starts with 2- [ (2,4-dichlorobenzyl) oxy] -2 - (2,4-dichlorobenzyl) ethyl. Among them, (2,4-dichlorobenzyl) means that the 2nd and 4th positions of the benzyl group are replaced by chlorine atoms. There are two structures. One is connected to the main chain through oxygen atoms to form an ether bond; the other is directly connected to the 2nd carbon atom of the main chain.
    In this way, the parts are structurally connected to form a unique chemical structure of 1 - {2 - [ (2,4 - dichlorobenzyl) oxy] - 2 - (2,4 - dichlorobenzyl) ethyl} - 1H - indole - 3 - formic anhydride (1:1). The parts of this structure interact to give the compound specific chemical and physical properties.
    What are the physical properties of 1- {2- [ (2,4-dichlorobenzyl) oxy] 2- (2,4-dichlorophenyl) ethyl} -1H-imidazole nitrate (1:1)
    1 - {2 - [ (2,4 -dihydroxyphenyl) oxy] -2 - (2,4 -dihydroxyphenyl) ethyl} -1H -indole-3 -carboxylic anhydride (1:1) is an organic compound. It has some unique physical properties.
    Looking at its properties, at room temperature, this compound may be in a solid state, mostly powdery, delicate and uniform, easy to use and manipulate. In terms of color, it may be white to light yellow, with pure color and no variegated doping.
    In terms of solubility, the compound has different solubility in organic solvents. In common organic solvents, such as ethanol and acetone, or have a certain solubility, it can form a uniform solution, which is conducive to its function as a reactant or product in organic synthesis reactions, and is also easy to separate and purify. However, in water, its solubility is poor, insoluble or slightly soluble. Due to the large proportion of hydrophobic groups in the molecular structure, it has a weak interaction with water molecules.
    Melting point is also an important physical property. Its melting point is in a specific temperature range, which may be the critical temperature for the compound to change from solid to liquid. Knowing the melting point accurately helps to identify the purity of the compound. The melting point of the pure product is relatively fixed. If it contains impurities, the melting point may decrease and the melting range becomes wider.
    In addition, the density of the compound is slightly higher than that of common organic solvents. In the solution system, its distribution and diffusion may be affected by density differences. Its stability cannot be ignored. In normal temperature and pressure, protected from light and dry environments, the compound may maintain stable structure and properties; in case of high temperature, strong light or specific chemical substances, or chemical reactions occur, resulting in changes in structure and properties.
    What is the main use of 1- {2- [ (2,4-dichlorobenzyl) oxy] 2- (2,4-dichlorophenyl) ethyl} -1H-imidazole nitrate (1:1)
    1 - {2 - [ (2,4 -dinitrophenyl) oxy] -2 - (2,4 -dinitrophenyl) ethyl} -1H -imidazole-4,5 -diformic anhydride is an important chemical substance in the field of organic synthesis. It has many main uses and is often used as a key intermediate in the field of medicinal chemistry to help create new drugs. Due to its special molecular structure, it can undergo various chemical reactions and skillfully combine with other compounds to construct drug molecules with specific biological activities, opening up new avenues for the treatment of diseases.
    In the field of materials science, it also shows unique value. Using this as a raw material can prepare polymer materials with excellent performance. Due to its structure endowing materials with specific physical and chemical properties, such as enhancing the stability of materials and improving their electrical properties, the resulting materials can be used in high-end fields such as electronic devices and aerospace.
    In addition, in the study of organic synthetic chemistry, this substance is an important synthetic building block and can participate in the construction of complex organic molecules. Chemists can precisely modify and modify its structure to achieve fine regulation of the structure and properties of the target product, and promote the development and progress of organic synthetic chemistry. In fact, it is indispensable and important in many fields.
    What are the synthesis methods of 1- {2- [ (2,4-dichlorobenzyl) oxy] 2- (2,4-dichlorophenyl) ethyl} -1H-imidazole nitrate (1:1)
    The synthesis method of 1 - {2- [ (2,4 -dinitrophenyl) oxy] -2 - (2,4 -dinitrophenyl) ethyl} -1H -imidazole-4 -carboxylic anhydride (1:1) is a very important research content in the field of organic synthesis. The synthesis method has been studied by many parties in the past, and now it is your way.
    One method can first introduce (2,4 -dinitrophenyl) oxy groups with appropriate starting materials and through specific reaction conditions. For example, a certain type of compound containing active hydrogen is selected to undergo a nucleophilic substitution reaction with (2,4-dinitrophenyl) halides in a suitable organic solvent in the presence of an alkaline catalyst. This reaction requires precise control of the reaction temperature and time. If the temperature is too high or the time is too long, it may cause side reactions and reduce the yield; if the temperature is too low or the time is too short, the reaction will not be complete.
    After the successful introduction of the (2,4-dinitrophenyl) oxygen group, the next step of the reaction can be carried out. Another compound containing a specific functional group can be used to react with the previous product to introduce the (2,4-dinitrophenyl) ethyl group. This step of the reaction may require the help of a specific catalyst, and the pH of the reaction system is also required.
    As for the construction of the 1H-imidazole-4-carboxylic anhydride part, it can be achieved by performing an appropriate carboxylation reaction on the compound containing the imidazole structure, and then dehydrating and other steps. In this process, the dehydration conditions are crucial, and a suitable dehydrating agent needs to be selected to control the reaction temperature and pressure, so that the reaction can proceed in the direction of generating the target product.
    In the synthesis process, each step of the reaction product needs to be carefully separated and purified. The commonly used methods include column chromatography and recrystallization to ensure the smooth progress of the subsequent reaction and the purity of the final product. In this way, after multiple steps of delicate reaction, 1 - {2 - [ (2,4 - dinitrophenyl) oxy] -2 - (2,4 - dinitrophenyl) ethyl} -1H - imidazole - 4 - carboxylic anhydride (1:1) can be obtained.
    1- {2- [ (2,4-dichlorobenzyl) oxy] 2- (2,4-dichlorophenyl) ethyl} -1H-imidazole nitrate (1:1) What are the precautions during use?
    1 - {2 - [ (2,4 -dihydroxyphenyl) oxy] - 2 - (2,4 -dihydroxyphenyl) ethyl} -1H -indazole-3 -carboxylic anhydride (1:1) is a complex chemical substance, and there are many points to pay attention to during use.
    First of all, this chemical substance has specific chemical activities and reaction characteristics. Because its structure contains a variety of functional groups, such as hydroxy, indazole and carboxylic anhydride, when mixed or reacted with other substances, it is easy to undergo substitution, addition, hydrolysis and other reactions. Therefore, it is necessary to precisely control the reaction conditions, such as temperature, pH, reaction time, etc. If the temperature is too high or too low, it may cause abnormal reaction rate and affect product formation; if the pH is not suitable, it may cause the reaction direction to deviate from expectations, or even cause side reactions.
    Secondly, the substance may have certain toxicity and danger. Be sure to strictly follow the safety operating procedures during use and take protective measures. Wear appropriate protective equipment, such as laboratory clothes, gloves, protective glasses, etc., to avoid skin contact and eye splashing. In case of inadvertent contact, rinse with plenty of water immediately and seek medical attention according to the specific situation.
    In addition, storage should also be paid attention to. Store in a dry, cool and well-ventilated place, away from fire sources and oxidants. Due to the particularity of its structure, damp or high temperature, strong oxidizing agents may cause serious consequences such as deterioration, decomposition and even explosion.
    In addition, when taking and weighing, precise instruments and equipment should be used to ensure the accuracy of the dosage. Minor dosage deviations may also have a significant impact on the results in some reactions or experiments with strict dosage requirements.
    In conclusion, when using 1 - {2 - [ (2,4 - dihydroxyphenyl) oxy] - 2 - (2,4 - dihydroxyphenyl) ethyl} - 1H - indazole - 3 - carboxylic anhydride (1:1), it is necessary to pay full attention to its chemical properties, safety risks, storage conditions and operating specifications, and operate with caution to ensure the smooth progress of the experiment or production.