2 1 Benzofuran 2 Yl 4 5 Dihydro 1h Imidazole
quinoline thiophene imidazole thiazole

2-(1-benzofuran-2-yl)-4,5-dihydro-1H-imidazole

    Specifications

    HS Code

    387976

    Chemical Formula C11H10N2O
    Molecular Weight 186.21 g/mol
    Appearance Solid (predicted, actual may vary based on purity and conditions)
    Melting Point Data may vary, needs experimental determination
    Boiling Point Data may vary, needs experimental determination
    Solubility In Water Low solubility expected (due to non - polar benzofuran and relatively non - polar imidazole parts)
    Solubility In Organic Solvents Likely soluble in common organic solvents like dichloromethane, chloroform, etc.
    Pka Data may vary, depends on the acidic or basic nature of the functional groups in different environments
    Logp Positive value expected (lipophilic due to aromatic rings)
    Stability Stable under normal conditions, but may react with strong oxidizing or reducing agents

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    General Information
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    Frequently Asked Questions

    As a leading 2-(1-benzofuran-2-yl)-4,5-dihydro-1H-imidazole 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 2- (1-benzofuran-2-yl) -4,5-dihydro-1H-imidazole?
    The question of this chemical structure needs to be solved in the quaint and elegant style of "Tiangong Kaiwu".
    The structure of "2- (1-naphthalimidazole-2-yl) -4,5-dihydro-1H-pyrazole" is related to the chemical essence. This compound, the naphthalimidazole part, is connected to the naphthalene ring and the imidazole ring. The naphthalene ring has the structure of a fused ring aromatic hydrocarbon and has a conjugated system to increase its stability. The imidazole ring contains nitrogen atoms and has certain basicity and reactivity.
    And the "4,5-dihydro-1H-pyrazole" part, the pyrazole ring has two adjacent nitrogen atoms, and the state of dihydrogen indicates that it is partially unsaturated. In the overall structure, each part affects each other. The connection between naphthalimidazole and pyrazole determines its spatial configuration and electron cloud distribution.
    In this structure, the atoms are connected by covalent bonds to form a stable structure. The electronic effects of different groups, such as induction effect and conjugation effect, affect its chemical properties. The conjugation of aromatic rings makes the electron cloud delocalized and affects the activity of electrophilic and nucleophilic reactions. Nitrogen atoms are solitary to electrons, or participate in the reaction, or affect the polarity and solubility of molecules.
    The spatial structure is also important. The relative positions of each group determine the intermolecular interactions, such as hydrogen bonds, van der Waals forces, etc., which have an impact on the crystal structure and solution behavior. In short, the chemical structure of this "2- (1-naphthalimidazole-2-yl) -4,5-dihydro-1H-pyrazole" is cleverly combined by various groups, and its characteristics are derived from the interaction between atoms and groups in the structure, which is the key to chemical investigation.
    What are the physical properties of 2- (1-benzofuran-2-yl) -4,5-dihydro-1H-imidazole?
    The physical properties of Guanfu 2- (1-naphthalimidazole-2-yl) -4,5-dihydro-1H-pyrazole are quite explainable.
    Its appearance is often a specific morphology, or crystalline, with a relatively regular texture. Under light, it may have a unique luster, as if it contains mysterious characteristics endowed by the microstructure. In terms of solubility, it shows different degrees of dissolution tendency in specific organic solvents. When encountering some polar solvents, it may be partially soluble, just like snowflakes melting into warm water and gradually dispersing in it, while in non-polar solvents, it may be insoluble, such as a rock in oil, which does not move at all. This is due to the difference in its molecular structure and the force between solvent molecules.
    Its melting point is also an important physical property. When the temperature gradually rises to a certain value, the substance changes from a solid state to a liquid state, just like ice and snow melting. This melting point value is stable, like the unique "ID card" of the substance, reflecting the strength of the interaction between molecules. In addition, density is also the key to consider. The mass of the material contained in each unit volume reveals the degree of tightness of the internal particle arrangement, or dense as lead, or loose as cotton, which is reflected in the density value.
    In terms of spectral characteristics, observed by a specific spectrometer, in the infrared spectrum, the vibration absorption peak of a specific chemical bond is like a unique music note, playing the melody of the material structure; in the nuclear magnetic resonance spectrum, hydrogen atoms or carbon atoms in different chemical environments, like choruses of different parts, each emits unique signals, providing strong clues for analyzing their fine structure. These physical properties, like pieces of a puzzle, together piece together the microscopic world of the substance 2- (1-naphthalimidazole-2-yl) -4,5-dihydro-1H-pyrazole.
    What are the main uses of 2- (1-benzofuran-2-yl) -4,5-dihydro-1H-imidazole?
    The main uses of 2 - (1 - gustraimidazole - 2 - yl) - 4,5 - dioxy - 1H - pyrazole are as follows:
    This compound has shown great application value in the field of medicinal chemistry. In the field of drug development, it can be used as a key lead compound. Due to its specific chemical structure, it can interact with specific targets in organisms. For example, studies have found that it may inhibit or activate some key enzymes, which play a key role in human physiological and pathological processes, such as participating in cell signaling, metabolic regulation, etc. For example, if it can inhibit an enzyme closely related to the proliferation of tumor cells, then it is expected to further develop new anti-tumor drugs based on this.
    In the field of pesticides, 2- (1-Ligonimidazole-2-yl) -4,5-dioxy-1H-pyrazole also has application potential. It may be able to affect the nervous system or physiological and metabolic pathways of some pests with its unique chemical activity, thus exerting insecticidal or deworming effects. In addition, due to the particularity of its structure, compared with traditional pesticides, it may have better environmental friendliness and selectivity. While effectively controlling pests, the harm to non-target organisms is relatively small, and the adverse impact on the ecological environment is reduced.
    In addition, in terms of materials science, this compound may be able to be used as a building block for functional materials. With its special electronic structure and chemical properties, it can endow materials with unique properties such as fluorescence and conductivity, and then be used in photoelectric materials, sensors and other fields. For example, through rational design and modification, it is possible to prepare fluorescent sensor materials with high sensitivity and selective identification ability for specific substances, which can be used to detect environmental pollutants or specific biomarkers in organisms.
    What are the synthesis methods of 2- (1-benzofuran-2-yl) -4,5-dihydro-1H-imidazole?
    To prepare 2- (1-naphthalimidazole-2-yl) -4,5-dihydroxy-1H-pyrrolizine, there are many synthesis methods, each with its own advantages. The following are selected:
    One is the cyclization condensation method. First, with suitable starting materials, through ingeniously designed reaction steps, each group in the molecule interacts and undergoes a cyclization condensation reaction. This process requires precise regulation of reaction conditions, such as temperature, pH, reaction time, etc. If the temperature is too high, it may cause side reactions to cluster and the product is impure; if the temperature is too low, the reaction rate will be slow and take a long time. Through careful control, the reaction proceeds along the expected path to build the basic skeleton of the target product.
    The second is the transition metal catalysis method. With the unique catalytic properties of transition metals, the formation of key chemical bonds can be effectively promoted. Transition metals are like magical batons that guide the orderly binding of reactant molecules. In this process, transition metal catalysts and their ligands need to be carefully selected. Different combinations have a great impact on the activity and selectivity of the reaction. Appropriate selection can greatly improve the yield and purity of the target product, but inappropriate combinations may cause the reaction to get into trouble or generate a large number of impurities.
    The third is biosynthesis. Using the special metabolic pathways of enzymes or microorganisms in the organism, the synthesis of the target product can be achieved under mild conditions. This method is green and environmentally friendly, with mild conditions and environmental friendliness. However, the biological system is complex, requiring in-depth understanding of relevant biological metabolic mechanisms, and the scale of biosynthesis is often limited. To achieve large-scale production, many technical problems need to be overcome.
    All this synthesis method has advantages and disadvantages. The cyclization method is classic and mature, and the conditions are properly controlled to obtain high yields; the transition metal catalysis method has good selectivity and can effectively construct complex structures; the biosynthesis method is green and mild, in line with the concept of sustainable development. The specific method to be selected depends on the actual situation, such as the availability of raw materials, cost considerations, product purity requirements, etc., to ensure that the synthesis path is cost-effective and the product is excellent.
    What are the precautions for storage and transportation of 2- (1-benzofuran-2-yl) -4,5-dihydro-1H-imidazole?
    2-%281-%E8%8B%AF%E5%B9%B6%E5%91%8B%E5%96%83-2-%E5%9F%BA%29-4%2C5-%E4%BA%8C%E6%B0%A2-1H-%E5%92%AA%E5%94%91 this chemical expression is confusing and it is difficult to specify the specific substance, the following answer is based on "what should be paid attention to in storage and transportation" in classical Chinese form:
    All things should be stored and transported with caution. First, it is related to the environment. It must be stored in a dry and cool place, away from direct sunlight, to prevent it from changing due to heat or causing danger. If it is easy to deliquescent, it needs to be tightly sealed and do not allow moisture to invade it.
    Second, about packaging. When using suitable equipment, it should be strong and tight to prevent leakage. In case of corrosive, the packaging material must be resistant to erosion, so as not to damage and hurt objects and people.
    Third, when transporting, pay attention to stability. Driving or boating should be smooth, avoid bumps and vibrations, and avoid damage to objects due to impact. And different things should be placed in categories, so as not to mix and cause chemical reactions.
    Fourth, the handling of personnel. Those who are in charge of storage and transportation must be familiar with the nature of things and follow the rules. In case of emergencies, they can also deal with it calmly, keeping things safe and protecting people's integrity. In this way, they can be stored and transported securely.