2 2 Bis 2 Chlorophenyl 4 4 5 5 Tetraphenyl 2 H 1 2 Biimidazole
quinoline thiophene imidazole thiazole

2,2'-bis(2-chlorophenyl)-4,4',5,5'-tetraphenyl-2'H-1,2'-biimidazole

    Specifications

    HS Code

    425387

    Chemical Formula C48H32Cl2N4
    Molecular Weight 729.69 g/mol
    Appearance Solid (usually powder)
    Physical State Solid at room temperature
    Melting Point Specific value would require literature search
    Solubility Poorly soluble in water, soluble in some organic solvents like DMSO
    Stability Stable under normal conditions, but may react with strong oxidizing agents
    Purity Can be obtained in various purity levels, e.g., 95%, 98% etc. depending on synthesis and purification methods

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    General Information
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    Frequently Asked Questions

    As a leading 2,2'-bis(2-chlorophenyl)-4,4',5,5'-tetraphenyl-2'H-1,2'-biimidazole 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 '-bis (2-chlorophenyl) -4,4', 5,5 '-tetraphenyl-2' H-1,2 '-biimidazole
    2% 2C2% 27 - bis% 282 - chlorophenyl% 29 - 4% 2C4% 27% 2C5% 2C5% 27 - tetraphenyl - 2% 27H - 1% 2C2% 27 - biimidazole, Chinese name is often 2,2 '-bis (2-chlorophenyl) -4,4', 5,5 '-tetraphenyl-2' H-1,2 '-biimidazole. The main application fields of this compound are as follows:
    One is the field of materials science. In this field, it is often used as a key component of organic optoelectronic materials due to its unique molecular structure. In the manufacture of organic Light Emitting Diode (OLED), it can act as a luminescent layer or a transport layer material. Due to the conjugated structure in the molecule, it can effectively absorb and emit light of specific wavelengths, thereby improving the luminous efficiency and color purity of OLED devices. For example, in the development of some new display technologies, after the introduction of this compound, the display color of the screen is more vivid and the contrast is also improved.
    Second, in the field of chemical analysis. It can be used as a special chemical probe. With its selective interaction with specific metal ions or organic molecules, it can achieve high sensitivity detection of certain substances. For example, in the detection of heavy metal ions in environmental water samples, it can react with specific heavy metal ions, accompanied by changes in color or fluorescence signal, in order to qualitatively or quantitatively analyze the content of heavy metal ions in water samples, providing an effective means for environmental monitoring.
    The third is in the field of pharmaceutical chemistry. Although there are relatively few related studies, its structural characteristics provide new ideas for drug design. Its complex imidazole structure can be used as a carrier for active groups. By modifying its structure, it is possible to develop new drugs with unique pharmacological activities, opening up potential directions for new drug research and development.
    What are the synthesis methods of 2,2 '-bis (2-chlorophenyl) -4,4', 5,5 '-tetraphenyl-2' H-1,2 '-biimidazole
    2% 2C2% 27 - bis% 282 - chlorophenyl% 29 - 4% 2C4% 27% 2C5% 2C5% 27 - tetraphenyl - 2% 27H - 1% 2C2% 27 - biimidazole is 2,2 '-bis (2-chlorophenyl) -4,4', 5,5 '-tetraphenyl-2' H-1,2 '-biimidazole. The synthesis method is as follows:
    To prepare this product, first take an appropriate amount of 2-chlorobenzaldehyde and acetophenone, use alcohol as solvent, add an appropriate amount of basic catalyst, such as potassium hydroxide or sodium hydroxide, control the temperature at 50-80 ℃, and stir the reaction number. In this step, the aldehyde and ketone are condensed to obtain the intermediate chalcone compound.
    Then, the obtained chalcone and phenylhydrazine are used as raw materials, glacial acetic acid is used as a solvent, and a little zinc powder is added as a catalyst. When the reflux number is heated. Zinc powder helps phenylhydrazine and chalcone to cyclize to form an intermediate containing an imidazole ring.
    Then take the obtained imidazole intermediate, add an appropriate oxidizing agent, such as active manganese dioxide or ammonium persulfate, in an organic solvent such as toluene or dichloromethane, control the temperature at 40-60 ° C, and stir the reaction. After oxidative coupling, the two imidazole units are connected to obtain 2,2 '-bis (2-chlorophenyl) -4,4', 5,5 '-tetraphenyl-2' H-1,2 '-imidazole.
    After the reaction is completed, the product can be separated and purified by conventional methods, such as extraction, column chromatography or recrystallization, to obtain a pure target product. During operation, pay attention to the control of reaction conditions to ensure that each step is sufficient to improve the yield and purity of the product.
    What are the physical and chemical properties of 2,2 '-bis (2-chlorophenyl) -4,4', 5,5 '-tetraphenyl-2' H-1,2 '-biimidazole
    2% 2C2% 27 - bis% 282 - chlorophenyl% 29 - 4% 2C4% 27% 2C5% 2C5% 27 - tetraphenyl - 2% 27H - 1% 2C2% 27 - biimidazole, this is an organic compound. Its physical and chemical properties are quite critical, which is related to its application in many fields.
    Looking at its physical properties, it is mostly solid at room temperature and pressure. The melting point of this compound may be in a specific temperature range due to the interaction and structure between molecules. There are many aromatic ring structures in the molecule, resulting in strong intermolecular forces and relatively high melting points. Its solubility may exhibit different behaviors in organic solvents. Due to its many hydrophobic groups such as benzene rings, it may have good solubility in non-polar organic solvents, such as toluene and chloroform; however, in polar solvents, such as water, the solubility may be poor.
    When it comes to chemical properties, the imidazole ring structure in the compound has a certain alkalinity. Due to the presence of lone pair electrons on the nitrogen atom, protons can be accepted. This basic property may play an important role in some chemical reactions, such as acid-base neutralization and catalytic reactions. At the same time, the presence of chlorine atoms in the molecule makes the compound have certain reactivity. Chlorine atoms can participate in nucleophilic substitution reactions and interact with nucleophiles to realize the conversion of functional groups, thereby deriving a variety of chemical derivatives and expanding their application scope. And because of its many benzene ring structures, the compounds have certain conjugated systems, or exhibit special optical and electrical properties, which may have potential uses in the field of optoelectronic materials.
    What is the price of 2,2 '-bis (2-chlorophenyl) -4,4', 5,5 '-tetraphenyl-2' H-1,2 '-biimidazole in the market?
    I don't know what you said about "2% 2C2% 27 - bis% 282 - chlorophenyl% 29 - 4% 2C4% 27% 2C5% 2C5% 27 - tetraphenyl - 2% 27H - 1% 2C2% 27 - biimidazole" on the market price. This is a very professional chemical substance, and its price is often affected by many factors.
    First, purity has a great impact. If the purity is very high, it is almost perfect, and there is no impurity interference, the price will be high; on the contrary, if the purity is low and there are many impurities, the price may drop.
    Second, the yield is also the key. If the preparation of this product is difficult and the output is scarce, the so-called "rare is more expensive", its price will be high; if the preparation process is mature and the output is considerable, the price may become more affordable.
    Third, market demand also affects the price. If many industries have strong demand for it, demand exceeds supply, and prices rise; if demand is low, supply exceeds demand, and prices may decline.
    Fourth, the price varies depending on the manufacturer. Manufacturers with high reputation and excellent craftsmanship have good product quality and high prices; new factories or unknown factories may have an advantage in order to compete for the market.
    To know the exact price of this product, you need to consult merchants in the chemical raw material market or chemical product trading platforms to obtain accurate numbers.
    How is the stability of 2,2 '-bis (2-chlorophenyl) -4,4', 5,5 '-tetraphenyl-2' H-1,2 '-biimidazole
    2% 2C2% 27 - bis% 282 - chlorophenyl% 29 - 4% 2C4% 27% 2C5% 2C5% 27 - tetraphenyl - 2% 27H - 1% 2C2% 27 - biimidazole, this is an organic compound. The analysis of its stability needs to be viewed from many aspects.
    First, chemical bonds, this compound contains many carbon-carbon bonds, carbon-nitrogen bonds and carbon-chlorine bonds. The carbon-carbon bond is quite stable, because its bond energy is quite high, it requires more energy to break. The carbon-nitrogen bond is also quite stable, which is beneficial to the maintenance of molecular structure. However, compared with the carbon-chlorine bond, the stability is slightly inferior. The chlorine atom has a certain electronegativity, or the carbon-chlorine bond has a certain polarity. Under certain conditions, it may easily react and cause molecular structure changes.
    The second time looking at the spatial structure, the molecular structure of this compound is complex, containing multiple phenyl groups and imidazole rings. The large spatial structure enhances the intermolecular force, which increases its stability to a certain extent. However, the complex structure may also cause tension in the molecule. If the tension is too large, it may affect its stability. When the external conditions are suitable, the molecule may change the configuration to reduce the tension. This process may involve the breaking and formation of chemical bonds.
    Furthermore, environmental factors have a great impact on its stability. At high temperatures, the thermal motion of molecules intensifies, and the vibration of chemical bonds increases. When the energy reaches a certain level, the chemical bonds may break, causing the compound to decompose. In case of strong acids and bases, the compound contains nitrogen and other atoms that can interact with acid and base, or undergo acid-base reactions, changing the molecular structure. If there is a specific oxidizing agent or reducing agent, it will affect its stability according to the oxidation state of each atom in the compound, or the redox reaction will occur.
    Light is also an important factor. Light energy of a specific wavelength may be absorbed by the compound, causing electron transitions, triggering photochemical reactions, and changing the structure of the compound. Therefore, in order to maintain the stability of this compound, it is necessary to control temperature, avoid acid and base and strong oxidative reducing agents, and prevent light.