1h Imidazole 5 Carboxaldehyde 4 1 1 Dimethylethyl
quinoline thiophene imidazole thiazole

1H-Imidazole-5-carboxaldehyde, 4-(1,1-dimethylethyl)-

    • Product Name 1H-Imidazole-5-carboxaldehyde, 4-(1,1-dimethylethyl)-
    • Alias 4-tert-Butyl-1H-imidazole-5-carbaldehyde
    • Einecs 68507-62-0
    • Mininmum Order 1 g
    • Factory Site West Ujimqin Banner, Xilingol League, Inner Mongolia, China
    • Price Inquiry sales9@alchemist-chem.com
    • Manufacturer Taiy Chemical
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    Specifications

    HS Code

    869265

    Chemical Formula C9H12N2O
    Molar Mass 164.204 g/mol
    Physical State Solid (predicted from structure and similar compounds)
    Solubility In Water Low (due to non - polar tert - butyl group and relatively hydrophobic imidazole ring)
    Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform, acetone (due to its organic nature)

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    Frequently Asked Questions

    As a leading 1H-Imidazole-5-carboxaldehyde, 4-(1,1-dimethylethyl)- 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 1H-Imidazole-5-carboxaldehyde, 4- (1,1-dimethylethyl) -?
    4- (1,1-dimethylethyl) -1H-imidazole-5-formaldehyde, this material has unique chemical properties. Its appearance is often in a specific form, mostly crystalline or powder state, white or slightly colored, depending on the preparation and purity.
    In terms of physical properties, the melting point is a key characteristic. The melting point or at a specific temperature range, this temperature range depends on the strength of the intermolecular force. The molecular structure contains specific groups, and the interaction between molecules has its own characteristics, which affects the melting point. The boiling point is also determined by factors such as the attractive force between molecules and the molecular mass, reflecting the energy required to change from liquid to gas.
    Solubility is also an important property. In common organic solvents, such as ethanol and dichloromethane, because their structures contain polar and non-polar parts, they may have a certain solubility according to the principle of similar miscibility. The polar imidazole ring can form a specific interaction with the polar solvent molecule to promote dissolution; the non-polar tert-butyl group affects the solubility. In water, its solubility may be limited due to the degree of polarity of the whole molecule.
    Chemically active, aldehyde group is its key active site. The aldehyde group can participate in many chemical reactions, such as oxidation reaction, can be oxidized to the corresponding carboxylic acid, and the selection of suitable oxidants, such as mild weak oxidants, can achieve this conversion. In the reduction reaction, aldehyde groups can be reduced to alcohols, and different reducing agents and reaction conditions can obtain different reduction products. In addition, aldehyde groups can condensate with compounds containing active hydrogen to form new carbon-carbon or carbon-heteroatomic bonds and expand molecular structures. Although tert-butyl groups in molecules are relatively stable, they can affect the molecular spatial resistance and electron cloud distribution, which in turn affect the overall chemical reaction activity and selectivity.
    What is the main use of 1H-Imidazole-5-carboxaldehyde, 4- (1,1-dimethylethyl) -?
    4- (1,1-dimethylethyl) -1H-imidazole-5-formaldehyde, this substance has a wide range of uses. In the field of medicinal chemistry, it is often used as a key intermediate. Due to its unique chemical structure, it can participate in a variety of chemical reactions and help synthesize compounds with specific biological activities, such as some therapeutic drugs for specific diseases. In the creation process, this is used as the starting material, and through a series of delicate transformations, the final product with significant pharmaceutical effect is obtained.
    In the field of materials science, it also has its uses. It may be integrated into polymer material synthesis to give new properties to the material. Because of its aldehyde group and imidazole ring properties, it may improve the stability and adsorption of the material. For example, when preparing adsorption materials with special functions, with the help of its structural advantages, the adsorption capacity of the material to specific substances can be improved, so that the material can play a role in environmental purification, material separation, etc.
    In the field of organic synthesis, it is even more indispensable. As an important synthetic building block, it can react with many organic reagents to build complex organic molecular structures. Chemists can follow a specific reaction path and use it to cleverly build carbon-carbon bonds or carbon-heteroatom bonds, paving the way for the synthesis of novel and unique functional organic compounds, and promoting the continuous development of organic synthesis chemistry.
    What are the synthesis methods of 1H-Imidazole-5-carboxaldehyde, 4- (1,1-dimethylethyl) -
    The method of synthesizing 4- (1,1-dimethylethyl) -1H-imidazole-5-formaldehyde can be obtained from many ways.
    One, or from a suitable starting material, can be achieved by the conventional reaction path of organic synthesis. First, take the imidazole derivative with the corresponding substituent and modify it to introduce the aldehyde functional group. If the imidazole compound containing tert-butyl is selected, the imidazole ring is halogenated at a specific position by halogenation reaction. This halogen atom can be used as the activity check point for subsequent reactions. Then a metal reagent, such as organolithium or Grignard reagent, interacts with the halimidazole derivative to generate the corresponding metal-organic intermediate. Then the intermediate is reacted with a suitable carbonyl source, such as N, N-dimethylformamide (DMF), and the aldehyde group is introduced into the imidazole ring by the nucleophilic addition mechanism, so as to obtain the target product 4- (1,1-dimethylethyl) -1H-imidazole-5-formaldehyde.
    Second, another way can also be found. From the perspective of constructing the imidazole ring, nitrile compounds containing tert-butyl and diamines are selected, and under suitable reaction conditions, the cyclization reaction is carried out to construct the skeleton of the imidazole ring. Then, by suitable oxidation means, the specific group on the imidazole ring is oxidized to an aldehyde group. For example, a mild oxidizing agent can be used to achieve the conversion to an aldehyde group under precise control of the reaction conditions to achieve the purpose of synthesis.
    Third, or a synthesis strategy with similar structures in the reference literature can be used. According to the structural characteristics of the target product, the existing method is slightly improved. If the reaction solvent, temperature, catalyst and other factors are considered in detail, the reaction conditions are optimized, the reaction yield and selectivity are improved, and the synthesis path is more efficient and convenient, so as to synthesize 4- (1,1-dimethylethyl) -1H-imidazole-5-formaldehyde.
    1H-Imidazole-5-carboxaldehyde, 4- (1,1-dimethylethyl) - is used in which areas
    1H-imidazole-5-formaldehyde, 4- (1,1-dimethylethyl), this substance has a wide range of uses and is used in many fields.
    In the field of pharmaceutical chemistry, it is often the key intermediate for the synthesis of drugs. The structure of Geinimidazole has unique chemical activity and can react with a variety of compounds to construct complex drug molecular structures. With its characteristics, it may be able to synthesize drugs with specific pharmacological activities, such as antibacterial and antiviral drugs, opening up new paths for pharmaceutical research and development.
    In the field of materials science, it also plays an important role. It can participate in the preparation of special functional materials, such as materials with specific adsorption and catalytic properties. Due to the presence of active aldehyde groups and specific substituents in the molecular structure, it can endow materials with unique properties, playing a key role in adsorption separation and catalytic reaction systems, and helping to improve material properties and efficiency.
    In the field of organic synthetic chemistry, it is an extremely important synthetic building block. Chemists use it as a starting material by ingeniously designing reaction routes to build complex organic molecular frameworks through various organic reactions, such as nucleophilic addition and condensation. It provides an effective way to synthesize new organic compounds and promotes the development of organic synthetic chemistry.
    This compound has important application value in many fields such as medicine, materials and organic synthesis. It is like a key to opening many scientific and technological doors, helping researchers explore more unknown fields and create more beneficial results.
    What is the market outlook for 1H-Imidazole-5-carboxaldehyde, 4- (1,1-dimethylethyl) -?
    Guanfu 1H-imidazole-5-formaldehyde, 4- (1,1-dimethylethyl) is an interesting topic in today's market prospects.
    At present, the field of chemical pharmaceuticals is booming, and this compound may emerge in the meantime. Due to its unique structure, it can be used as a key raw material for organic synthesis to create various new drugs. In the process of drug development, seeking molecules with unique activity and potential is a top priority. This imidazole derivative, or with its special chemical structure, precisely fits with the target in the organism, showing the efficacy of treating diseases. Therefore, in the eyes of pharmaceutical companies, it may be the key to opening the door to new drug research and development, and it is expected to give birth to many innovative drugs, which will benefit human health and well-being.
    Furthermore, there are many potential applications in the field of materials science. With the development of science and technology, the demand for special performance materials is increasing day by day. This compound may be ingeniously designed and modified due to its unique chemical properties, and integrated into various materials, giving the material advantages such as enhanced stability and improved optical properties. For example, in the synthesis of new polymer materials, it may be able to optimize the structure and properties of materials and broaden the application range of materials, from electronic devices to aerospace.
    However, its market prospects are not entirely smooth. The process of synthesizing this compound may face many technical problems and cost constraints. To achieve large-scale production, it is necessary to overcome technical bottlenecks and optimize the synthesis process to reduce costs and enhance product competitiveness. And market acceptance and recognition also need time to cultivate. Many wold-be users, such as pharmaceutical manufacturers, material research and development enterprises, need to have a deep understanding of its performance and advantages before they can adopt it.
    To sum up, although 1H-imidazole-5-formaldehyde, 4- (1,1-dimethyl ethyl) faces challenges, its potential in the fields of pharmaceuticals and materials science makes it quite promising. If we can properly deal with the difficulties, we will be able to win a place in the future market.