2 Phenylimidazo 1 2 A Pyrazine
pyridine pyrrole pyrazine piperidine piperazine

2-phenylimidazo[1,2-a]pyrazine

    Specifications

    HS Code

    550228

    Chemical Formula C12H8N4
    Molar Mass 208.22 g/mol
    Appearance Solid (color depends on purity and crystal form)
    Melting Point Data needed from literature
    Boiling Point Data needed from literature
    Solubility In Water Low solubility (organic compound, non - polar nature)
    Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform
    Density Data needed from literature
    Uv Vis Absorption Absorbs in the ultraviolet - visible region, λmax data needed from literature
    Fluorescence Properties May exhibit fluorescence, quantum yield data needed from literature

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    Frequently Asked Questions

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    What are the physical properties of 2-phenylimidazo [1,2-a] pyrazine?
    2-Phenylimidazo [1,2-a] pyrazine is an organic compound. The physical properties of this compound are very important for its application in various fields.
    Looking at its appearance, 2-phenylimidazo [1,2-a] pyrazine is often in a solid state at room temperature and pressure. Its color may be white to light yellow powder, which makes it easy to identify and handle in many reactions and preparations.
    The melting point of 2-phenylimidazo [1,2-a] pyrazine has been determined by many experiments to be within a certain range. This melting point data is crucial because it can be used to judge the purity of the compound and predict its behavior during heating. The determination of the melting point is often a key step in the identification and characterization of this compound.
    Solubility is also one of the important physical properties of 2-phenylimidazo [1,2-a] pyrazine. It exhibits good solubility in organic solvents such as dichloromethane and chloroform. This property makes it possible to choose such solvents as reaction media during organic synthesis to help the reaction proceed smoothly. However, its solubility in water is poor, due to the dominant hydrophobic groups in the molecular structure of the compound, which makes it interact weakly with water molecules.
    Furthermore, the density of 2-phenylimidazo [1,2-a] pyrazine also has a specific value. Density is a basic physical property of a substance. When preparing and applying this compound, it plays an indispensable role in precise measurement and determination of its proportion in the mixture.
    In addition, the compound has certain stability in the solid state, but under extreme conditions such as high temperature, strong acid or strong base, the structure may change. The understanding of this stability is extremely critical for the control of its storage and use environment.
    From the above, it can be seen that the physical properties of 2-phenylimidazo [1,2-a] pyrazine, such as appearance, melting point, solubility, density and stability, are interrelated and jointly determine its application potential and method in chemical synthesis, materials science and many other fields.
    What are the chemical properties of 2-phenylimidazo [1,2-a] pyrazine
    2-Phenylimidazolo [1,2-a] pyrazine, this is an organic compound. Its chemical properties are unique and worthy of investigation.
    First of all, its physical properties, under room temperature, or solid state, are mostly crystalline. Due to strong intermolecular forces, its melting point is relatively high. Appearance may be white to light yellow powder, depending on purity and crystallization conditions.
    Re-discussion of chemical activity, 2-phenylimidazolo [1,2-a] pyrazine contains imidazole and pyrazine heterocyclic structure, with a unique electron cloud distribution. The nitrogen atom of the imidazole ring has a solitary pair of electrons, which can be used as an electron donor to exhibit alkalinity and can react with acids to form corresponding salts. The pyrazine ring expands the entire molecular conjugation system and enhances its stability. At the same time, due to conjugation, the compound has characteristic absorption in the ultraviolet region, which can be identified and quantified by ultraviolet spectroscopy.
    Its aromaticity is significant, and the fused ring system composed of imidazole and pyrazine rings conforms to the Shock rule and has aromaticity. This property makes the molecule stable, less prone to addition reactions, and more prone to electrophilic substitution reactions. If under appropriate conditions, halogenation, nitrification, sulfonation and other electrophilic substitution reactions can occur on the benzene ring, and different functional groups can be introduced in organic synthesis to expand its derivatization path.
    The solubility of this compound cannot be ignored. Due to the hydrophobic benzene ring and heterocyclic structure of the molecule, the solubility in polar solvents such as water is limited, but it has good solubility in organic solvents such as chloroform, dichloromethane, N, N-dimethylformamide. This property needs to be considered when separating, purifying and selecting the reaction solvent.
    In addition, 2-phenylimidazolo [1,2-a] pyrazine may participate in cyclization, condensation and other reactions under specific conditions to further construct complex organic molecular structures, which has potential application value in pharmaceutical chemistry, materials science and other fields.
    What are the common synthesis methods of 2-phenylimidazo [1,2-a] pyrazine?
    The common synthesis methods of 2-phenylimidazolo [1,2-a] pyrazine cover various routes. One is obtained by the cyclization reaction of nitrogen-containing heterocycles. First, appropriate starting materials, such as compounds containing phenyl and pyrazine-related structures, are taken to undergo cyclization and condensation under specific reaction conditions. In this process, careful selection of reaction reagents and catalysts is required to promote the smooth progress of the cyclization reaction. If suitable alkali substances are selected, the pH of the reaction system can be adjusted to help the reaction advance towards the target product.
    Furthermore, it can be synthesized through a coupling reaction catalyzed by transition metals. In this method, transition metals (such as palladium, copper, etc.) are used as catalysts to couple different organic fragments with each other to construct the structure of 2-phenylimidazolo [1,2-a] pyrazine. This reaction requires precise control of reaction temperature, time and ratio of reactants in order to obtain higher yield products. At the same time, the choice of reaction solvent is also crucial, and suitable solvents can improve the solubility and reactivity of the reactants.
    In addition, there is a strategy for multi-step reaction synthesis. The parent nuclear structure of imidazolo [1,2-a] pyrazine is first synthesized, and then phenyl is introduced through substitution reaction. Each step of the reaction requires fine operation, and the reaction conditions are strictly controlled to ensure the selectivity and yield of the reaction. In this way, after multi-step transformation, 2-phenylimidazolo [1,2-a] pyrazine can be successfully prepared. In short, the synthesis of this compound requires comprehensive consideration of various reaction conditions and steps, and careful design of the synthesis route to achieve the desired goal.
    In which fields is 2-phenylimidazo [1,2-a] pyrazine used?
    2-Phenylimidazolo [1,2-a] pyrazine is useful in various fields.
    In the field of medicine, this compound has great potential. Its structure is unique, or it can be specifically combined with biological macromolecules in vivo to modulate the physiological and biochemical processes of the body. Medical research, hoping to make new drugs to treat diseases, such as the research of anti-tumor drugs. Cancer cells proliferate rapidly, 2-phenylimidazolo [1,2-a] pyrazine may inhibit the division of cancer cells and hinder their growth, contributing to the anti-cancer cause.
    In the field of materials science, it can also be used. This compound may have special optoelectronic properties and can be used to make new optoelectronic devices. If it can make good use of its characteristics, it can create a high-efficiency Light Emitting Diode to make the lighting light brighter and save energy; or it can be used for photovoltaic materials to improve the efficiency of solar energy conversion and find solutions to energy problems.
    In the field of organic synthesis, 2-phenylimidazole [1,2-a] pyrazine is the key intermediate. Organic synthesis craftsmen can use it to build complex organic molecules through clever reactions according to its structure. Based on this, expand the synthesis path, create a variety of organic compounds, and add brilliance to the chemical world.
    In the field of agriculture, it may have the effect of repellent and bacteriostatic. It can produce pesticides, protect crops from pest bacteria, protect harvests, and maintain the prosperity of agriculture. < Br >
    2-Phenylimidazolo [1,2-a] pyrazine is hidden like a pearl in many fields such as medicine, materials, organic synthesis, agriculture, etc. It is waiting for everyone to tap its potential and develop its extraordinary uses for human well-being.
    What is the market outlook for 2-phenylimidazo [1,2-a] pyrazine?
    2-Phenylimidazo [1,2-a] pyrazine is an organic compound. Its market prospect is related to many factors.
    From the perspective of the pharmaceutical field, this compound may have potential biological activity. In today's pharmaceutical research and development, organic molecules with special structures are often explored, hoping that it can provide opportunities for the creation of new drugs. If 2-phenylimidazo [1,2-a] pyrazine is proven to have positive effects in the treatment of diseases, such as anti-cancer, antiviral or neurological diseases, it will surely attract the attention of pharmaceutical companies, and the market prospect will be extremely broad. Many medical research teams are dedicated to exploring such potential compounds. If their activity is confirmed, the road to follow-up clinical trials and drug development will be long and difficult, but once successful, the market demand will be limitless.
    In the field of materials science, organic compounds are often the cornerstone of new materials. 2 - phenylimidazo [1,2 - a] pyrazine will also open up new markets if its unique structure can endow materials with special properties, such as excellent optical, electrical or thermal properties. For example, in the field of optoelectronic materials, compounds with special fluorescence or electrical conductivity can be used to fabricate high-efficiency Light Emitting Diodes, solar cells and other devices. If this compound is properly modified and applied to meet the material performance requirements, it will attract material companies to invest in R & D and production, and the market prospect is quite promising.
    However, its marketing activities also face challenges. The cost and process complexity of synthesizing the compound are key factors. If the synthesis route is long, harsh conditions and low yield, it will lead to high production costs and limit its large-scale production and market application. Furthermore, in-depth research on its properties and applications still requires time and resources. Scientific researchers need to fully explore its properties and potential uses in order to accurately evaluate the market value. This process may consume a lot of manpower, material resources and time.
    To sum up, 2 - phenylimidazo [1,2 - a] pyrazine has an addressable market opportunity, but to turn the potential into actual market success, scientific research and industry need to join hands to overcome the synthesis problem, in-depth exploration of performance, in order to develop its application in medicine, materials and other fields.