2 Butyl 4 Chloro 5 Formy Imidazole
quinoline thiophene imidazole thiazole

2-butyl-4-chloro-5-formy imidazole

    Specifications

    HS Code

    815220

    Chemical Formula C8H11ClN2O
    Molecular Weight 186.64
    Appearance Solid (predicted)
    Boiling Point 363.4°C at 760 mmHg (predicted)
    Melting Point 138 - 140°C
    Flash Point 173.6°C (predicted)
    Density 1.239 g/cm³ (predicted)
    Solubility In Water Insoluble (predicted)
    Logp 2.03 (predicted)
    Vapor Pressure 2.14E-06 mmHg at 25°C (predicted)

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    General Information
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    Frequently Asked Questions

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    What is the chemistry of 2-butyl-4-chloro-5-formy+imidazole?
    2-Butyl-4-chloro-5-formyl imidazole, this is an organic compound. It has many unique chemical properties.
    First, the imidazole ring in the molecule is a five-membered heterocyclic ring containing two nitrogen atoms, which endows it with certain aromaticity. The aromatic system makes the compound relatively stable, and the delocalization of π electrons can reduce the overall energy of the molecule.
    The presence of its 2-position butyl, because butyl is alkyl, has an electron-induced effect. This effect can increase the electron cloud density of the imidazole ring, which in turn affects the reactivity of the compound. In the electrophilic substitution reaction, the electron cloud density increases more easily to be attacked by electrophilic reagents. Although the chlorine atom at the
    4 position is a halogen atom, it has an electron-absorbing induction effect, which will reduce the electron cloud density of the imidazole ring. At the same time, the lone pair electrons of the chlorine atom can be p-π conjugated with the imidazole ring, and to a certain extent, it can disperse the positive charge on the ring, which has an impact on the reactivity and selectivity. The formyl group at the
    5 position is a functional group with strong electron-absorbing properties. It not only reduces the electron cloud density of the imidazole ring significantly and changes the electron distribution on the ring, but also causes many specific reactions due to the existence of carbon If it can react with nucleophiles, it can form acetals with alcohols, and imines with amines.
    In addition, the physical properties of this compound are also affected by various groups. Butyl increases the lipid solubility of molecules, while formyl groups can participate in intermolecular hydrogen bonding, contributing to physical properties such as melting point, boiling point and solubility.
    Due to the interaction of various groups, 2-butyl-4-chloro-5-formyl imidazole can be used as a key intermediate in the field of organic synthesis to construct more complex organic molecular structures.
    What are the common uses of 2-butyl-4-chloro-5-formy+imidazole?
    2-Butyl-4-chloro-5-formylimidazole is an organic compound that is very important in the field of organic synthesis. Its common uses are as follows:
    First, the field of drug synthesis. This compound can be used as a key intermediate for the creation of various drugs. The structural unit of imidazole is common in many bioactive molecules, and it may interact with specific targets in organisms. The specific substituents of 2-butyl-4-chloro-5-formylimidazole, such as butyl, chlorine atom and formyl group, can regulate the physicochemical properties and biological activities of molecules. Taking the development of anti-cancer drugs as an example, through structural modification and derivatization of the compound, new drug molecules with high selective inhibitory activity on cancer cells may be obtained.
    Second, the field of materials science. Due to its unique chemical structure, it may be able to participate in specific polymerization reactions, and then prepare polymer materials with special properties. For example, polymerization with other monomers containing active groups may generate polymers with special optical and electrical properties, which may have potential applications in the field of optoelectronic materials, such as organic Light Emitting Diode (OLED) materials.
    Third, it also has potential uses in the field of organic catalysis. Some groups in its molecular structure may exhibit catalytic activity, which can catalyze specific organic reactions, such as nucleophilic addition, cyclization, etc. With its unique electronic effect and steric resistance, it may achieve effective regulation of reaction selectivity and activity, providing an efficient catalytic pathway for organic synthesis.
    Fourth, in the design of new ligands. 2-butyl-4-chloro-5-formylimidazole can be modified and used as a ligand for metal complexes. After its coordination with metal ions, the formed complexes may emerge in the fields of catalysis, fluorescence sensing, etc. For example, in fluorescence sensing, specific metal ions or molecules can be specifically identified and detected, and sensitive detection of the target can be achieved by changing the fluorescence properties of the complex.
    What is 2-butyl-4-chloro-5-formy+imidazole synthesis method?
    To prepare 2-butyl-4-chloro-5-formyl imidazole, the following method can be used.
    Take suitable starting materials first, such as compounds containing butyl, chlorine and functional groups that can be converted into formyl groups. Often imidazole derivatives with appropriate substituents are used as the base materials.
    At the beginning of the reaction, a suitable halogenating agent, such as a chlorine-containing halogenating agent, can be selected to halogenate with imidazole derivatives to introduce chlorine atoms at specific locations. This halogenation reaction requires attention to the control of reaction conditions, such as temperature, solvent and catalyst use. Too high or too low temperature may affect the selectivity and yield of the reaction. A suitable solvent should be able to dissolve the reactants well and have no adverse effect on the reaction, and the catalyst can effectively promote the reaction.
    Then, for the introduction of butyl, an alkylation reaction can be used. Select an appropriate butylation reagent, and under suitable basic conditions and catalysts, the butyl is successfully attached to the imidazole ring. This step also requires precise regulation of the reaction parameters to ensure that the butyl is accurately connected to the target position to avoid side reactions.
    As for the introduction of formyl groups, a suitable formylation reagent can be selected. There are various common formylation methods, such as using carbon monoxide and a specific catalyst system to achieve formylation under suitable reaction conditions; or using other reagents containing formyl groups to react with imidazole derivatives in a specific reaction environment, so that the formyl group is smoothly connected to the designated position. During the whole reaction process, after each step of the reaction is completed, the product needs to be separated and purified by methods such as column chromatography and recrystallization to ensure the purity of the product in each step and lay a good foundation for the subsequent reaction. In this way, through multi-step reaction and fine operation, it is expected to achieve the synthesis of 2-butyl-4-chloro-5-formyl imidazole.
    What is the market price of 2-butyl-4-chloro-5-formy+imidazole?
    There is a question today about the market price of 2 - butyl - 4 - chloro - 5 - formy + imidazole. This is an organic chemical substance, and its market value is difficult to determine. The price of its price is determined by many reasons.
    First, the price of raw materials. The synthesis of this substance requires specific raw materials. If the price of raw materials is high, or the acquisition of raw materials is difficult, the cost of producing this substance will be high, and the market value will rise accordingly. Second, the difficulty of preparation. If the synthesis method is complicated, special instruments and reagents are required, or the reaction conditions are harsh, and many human, material and financial resources are required, the cost will increase and the market value will also be high. Third, the supply and demand of the market. If the product is in wide demand in the fields of medicine, chemical industry, etc., but the supply is limited, the price must be high; if the demand is small and the supply is large, the price must be low. Fourth, the scale of production. Large-scale production may reduce costs through scale effects, and the market value may be reduced; however, small-scale production, the cost is difficult to reduce, and the price may be high.
    And the name of this substance may be wrong. The "+" of "formy +" in "2-butyl-4-chloro-5-formy + imidazole" may be wrong. If it is "formyl" (formyl), it is the correct name. Due to limited information, it is difficult to determine the exact market value. It is necessary to check the chemical product trading platform in detail, consult professional chemical raw material suppliers, or refer to relevant industry reports to get a more accurate price.
    What are 2-butyl-4-chloro-5-formy+imidazole safety precautions?
    2-Butyl-4-chloro-5-formylimidazole, this is a chemical substance. Regarding its safety precautions, let me come one by one.
    First, protection needs to be thorough. This substance may be irritating to the eyes, skin and respiratory tract. Therefore, when operating, it is necessary to wear suitable protective equipment. Goggles can protect the eyes from splashing damage; gloves should be made of chemically resistant materials, such as nitrile gloves, to protect the skin of the hands; gas masks are also indispensable, especially in poorly ventilated areas, which can effectively filter harmful substances in the air and avoid inhalation hazards.
    Second, storage should be cautious. Be sure to keep it in a cool, dry and well-ventilated place. Keep away from fires and heat sources to prevent fires or exacerbate their chemical reactions. It should also be stored separately from oxidants, acids, alkalis, etc., because it coexists with them or causes violent reactions, which increases the danger.
    Third, the operation should be standardized. Operating in a fume hood can remove volatile harmful gases in time. When taking it, the action should be slow to avoid dust. If it is accidentally sprinkled, do not panic, and take proper cleaning measures immediately. A small amount of sprinkling can be collected in a dry and clean container with a clean shovel; if a large amount is sprinkled, it needs to be covered with inert materials to prevent the spread and then cleaned up.
    Fourth, emergency response should be well known. If you accidentally come into contact with the skin, you should rinse with a large amount of flowing water as soon as possible, and then seek medical treatment. If it splashes into the eye, you should immediately open the eyelids, rinse with flowing water or normal saline, and seek medical attention quickly. In case of inhalation, quickly move to a fresh air place to keep the respiratory tract unobstructed. If breathing difficulties require oxygen and breathing stops, artificial respiration should be administered immediately and medical attention should be sought.
    In short, when treating 2-butyl-4-chloro-5-formylimidazole, only by strictly observing safety procedures and being vigilant at all times can you prevent problems before they occur and ensure the safety of people and the environment.