2 2 2 1 3 5 Benzinetriyl Tris 1 Phenyl 1 H Benzimidazole
quinoline thiophene imidazole thiazole

2,2',2"-(1,3,5-benzinetriyl)-tris(1-phenyl-1-H-benzimidazole)

    Specifications

    HS Code

    756662

    Chemical Formula C63H42N6
    Molar Mass 907.04 g/mol
    Appearance Solid
    Solubility Insoluble in water
    Optical Properties May have fluorescence properties
    Chemical Reactivity Reacts with strong oxidizing agents

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    General Information
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    Frequently Asked Questions

    As a leading 2,2',2"-(1,3,5-benzinetriyl)-tris(1-phenyl-1-H-benzimidazole) 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 main application fields of 2,2 ', 2' - (1,3,5-phenyltriyl) -tris (1-phenyl-1-H-benzimidazole)
    2%2C2%27%2C2%27%27-%281%2C3%2C5-%E8%8B%AF%E4%B8%89%E5%9F%BA%29-%E4%B8%89%281-%E8%8B%AF%E5%9F%BA-1-H-%E8%8B%AF%E5%B9%B6%E5%92%AA%E5%94%91%29 this compound has shown unique application value in many fields.
    In the field of medicinal chemistry, it may have the potential to interact with biological targets due to specific chemical structures. For example, it can precisely bind to the activity check point of key enzymes to regulate the activity of enzymes, and then affect disease-related physiological processes. For some inflammatory diseases, it may play an anti-inflammatory effect by inhibiting the synthesis and release of inflammatory mediators; for tumor diseases, it may interfere with the proliferation signaling pathway of tumor cells and block tumor cell growth.
    In the field of materials science, it can be used as a key building block for functional materials. Due to their unique spatial structure and electronic properties, materials with special optical and electrical properties may be prepared through specific design and synthesis processes. For example, synthetic organic optoelectronic materials may have excellent fluorescence properties, suitable for light emitting diodes, biological imaging and other fields; or they may exhibit unique electrical conductivity, providing direction for the development of new conductive materials.
    In the agricultural field, there may also be application opportunities. Or it can be developed into new pesticides or plant growth regulators. By binding with specific receptors in plants, it regulates the growth and development process of plants, such as promoting seed germination and improving crop resistance; it may also have inhibitory or killing effects on some pests or pathogens, and because of its relatively unique chemical structure, it may reduce the negative impact on the environment, which is in line with the development needs of green agriculture.
    In summary, 2%2C2%27%2C2%27%27-%281%2C3%2C5-%E8%8B%AF%E4%B8%89%E5%9F%BA%29-%E4%B8%89%281-%E8%8B%AF%E5%9F%BA-1-H-%E8%8B%AF%E5%B9%B6%E5%92%AA%E5%94%91%29 has potential and wide application prospects in many fields such as medicine, materials, agriculture, etc., and is worthy of in-depth research and exploration.
    What is the synthesis method of 2,2 ', 2' - (1,3,5-phenyltriyl) -tris (1,3,5-phenyltriyl) -tris (1-phenyl-1-H-benzimidazole)
    To prepare 2,2 ', 2' - (1,3,5-phenyltriyl) -tris (1,3,5-phenyltriyl) -tris (1-phenyl-1 -H-benzimidazole), the following ancient method can be followed:
    First take 1,3,5-tribromobenzene as the starting material, and use palladium catalysis to perform Suzuki coupling reaction with phenylboronic acid. This reaction needs to be carried out in an alkaline environment, in a mixed solvent of toluene, ethanol and water, heated and refluxed. In this way, 1,3,5-tris (phenyl) benzene can be obtained. During the reaction, the amount of palladium catalyst, the type and amount of base, the ratio of solvent, and the reaction temperature and time need to be carefully adjusted to increase the yield and purity of the product. < Br >
    After obtaining 1,3,5-tris (phenyl) benzene, mix it with o-phenylenediamine, use polyphosphoric acid as catalyst and solvent, heat it to an appropriate temperature, and perform a condensation cyclization reaction to produce 1,3,5-tris (1-phenyl-1-H-benzimidazole-2-yl) benzene. In this step, the amount, reaction temperature and time of polyphosphoric acid have a significant impact on the reaction process and product formation, so it must be treated with caution.
    Finally, using 1,3,5-tris (1-phenyl-1 -H-benzimidazole-2-yl) benzene as raw material, again with palladium catalysis, and 1,3,5-tris (4,4,5,5-tetramethyl-1,3,2-dioxyboropentyl-2-yl) benzene, react under conditions similar to Suzuki coupling to obtain the target product 2,2 ', 2' - (1,3,5-phenyltriyl) -tris (1,3,5-phenyltriyl) -tris (1-phenyl-1 -H-benzimidazole). This step also requires strict control of the reaction conditions, such as catalyst dosage, alkali concentration, reaction temperature and duration, etc., in order to make the reaction smooth and obtain the ideal product.
    After each step of the reaction, the product needs to be purified by suitable separation and purification methods, such as column chromatography, recrystallization, etc., to remove impurities, improve the purity of the product, and then provide high-quality raw materials for the next reaction to ensure the success of the entire synthesis process.
    What are the physical properties of 2,2 ', 2' - (1,3,5-phenyltriyl) -tris (1-phenyl-1-H-benzimidazole)
    2%2C2%27%2C2%27%27-%281%2C3%2C5-%E8%8B%AF%E4%B8%89%E5%9F%BA%29-%E4%B8%89%281-%E8%8B%AF%E5%9F%BA-1-H-%E8%8B%AF%E5%B9%B6%E5%92%AA%E5%94%91%29 is a complex organic compound. The physical properties of this compound are related to its structure and composition, and have a profound impact on its behavior in a specific environment.
    Its appearance is often solid, mostly powdery or crystalline. The intermolecular forces promote the orderly arrangement of molecules, so a specific crystal structure is formed. Its color varies due to the presence of impurities and conjugated systems. In pure state, it is either colorless and transparent, or white. If the structure contains chromophores such as conjugated double bonds, it may show light yellow, light brown and other colors.
    Melting point is one of the important physical properties of this compound. Due to the existence of hydrogen bonds, van der Waals forces and other forces between molecules, in order to melt from a solid state to a liquid state, a certain amount of energy needs to be absorbed to overcome these forces. The compound has a complex molecular structure and strong intermolecular forces, so the melting point may be relatively high.
    In terms of solubility, its solubility in organic solvents may vary depending on the type of solvent. If an organic solvent can form similar forces between molecules of the compound, such as hydrogen bonds, van der Waals forces, etc., the solubility is better. In polar organic solvents, the solubility is also different due to the different degree of matching between molecular polarity and solvent polarity. In non-polar organic solvents, if the intermolecular dispersion force matches, there is also a certain solubility.
    Density is related to molecular weight and molecular arrangement. The compound has a complex structure, a large molecular mass, and a tight molecular arrangement, so the density may be larger.
    In addition, the compound may have specific optical properties. If the molecular structure contains a chiral center or is optically active, it can rotate the vibration direction of polarized light under polarized light. And because it contains a conjugated system or absorbs under specific wavelength light irradiation, it exhibits ultraviolet-visible absorption spectral characteristics.
    The above physical properties are of key significance for the synthesis, separation, identification and practical application of this compound. During synthesis, properties such as melting point and solubility can help to select suitable reaction conditions and solvents; during separation and purification, appropriate separation methods can be selected according to their solubility differences; during identification, appearance, melting point, optical properties, etc. can be used as an important basis.
    What is the chemical stability of 2,2 ', 2' - (1,3,5-phenyltriyl) -tris (1-phenyl-1-H-benzimidazole)?
    Nowadays, there are chemical substances called 2,2 ', 2' - (1,3,5-phenyltriyl) -tris (1-phenyl-1-H-benzimidazole). The chemical stability of this substance is related to its many characteristics, and it is also the key to explore.
    Looking at its molecular structure, the benzene ring is cleverly connected with the benzimidazole group, which is like a mortise and tenon joint, to build a unique structure. The benzene ring has a conjugated large π bond, which is quite stable and can provide a solid foundation for the whole molecule, just like the cornerstone of a building, making the molecular framework not easy to collapse. The benzimidazole group also has a conjugated system, which can interact with the conjugated system of the benzene ring to form a wider range of electron delocalization, which is like pulling the trigger and affecting the whole body, enhancing the stability of the molecule as a whole.
    Furthermore, from the perspective of chemical bond energy, the chemical bond between the atoms in the molecule may be a covalent bond, and the bond energy size determines the stability of the bond. Covalent bonds such as carbon-carbon bonds and carbon-nitrogen bonds in this substance have high bond energy and require greater energy to break them. This is also one of the important guarantees for the chemical stability of the substance, as if it is a strong armor for the molecule.
    In terms of steric hindrance, the large benzene ring and benzimidazole groups are intertwined in the spatial distribution, forming a certain spatial hindrance. When external substances want to react with the molecule, the steric hindrance will make it difficult for the reagent to approach the reaction check point, like many barriers, hindering the progress of the reaction, thereby maintaining the chemical stability of the molecule.
    In addition, intermolecular forces also affect its stability. Intermolecular forces such as van der Waals forces and hydrogen bonds may exist in this substance. Although the van der Waals force is relatively weak, the van der Waals force between many molecules is superimposed on each other, which should not be underestimated, just like countless filaments implicated in each other, making the molecular bonding more closely; if there is a hydrogen bond, the force is stronger, like a strong rope, which connects the molecules tightly and further improves the chemical stability of the substance.
    Overall, 2,2 ', 2' - (1,3,5-phenyltriyl) -tris (1-phenyl-1-H-benzimidazole) has high chemical stability due to its unique molecular structure, high bond energy, spatial resistance and intermolecular forces.
    What is the price range of 2,2 ', 2' - (1,3,5-phenyltriyl) -tris (1-phenyl-1-H-benzimidazole) in the market?
    This is a rare chemical named 2,2 ', 2' - (1,3,5-phenyltriyl) -tris (1-phenyl-1-H-benzimidazole). However, the price of this product in the market is difficult to determine. The price fluctuation is affected by many factors.
    First, the difficulty of production is the key. If the preparation method is complicated, the required raw materials are rare and difficult to obtain, and the process conditions are harsh, the cost will be high, and the price will be high.
    Second, the market supply and demand situation has a great impact. If there are many people who want it, the use of it is wide, but the output is limited, and the supply is in short supply, the price will rise; on the contrary, if there is little demand and excess supply, the price will decline.
    Third, the quality grade is also an important factor. Those with high purity and excellent quality often have higher prices than ordinary ones.
    Fourth, the difference in region also has an impact. In different places, due to transportation costs, tax policies, etc., the price may be different.
    To sum up, if you want to know the price range of this product in the market, you should carefully study the prices quoted by chemical raw material trading platforms and chemical product suppliers, or consult experts in the chemical industry to obtain a more accurate number. However, due to the above factors, it is difficult to determine the exact price range.