2,2'-Bis(O-Chlorophenyl)-4,4',5,5'-Tetraphenyl-1,2'-Bi (III-Imidazole)

2% 2C2% 27 -Bis (o-chlorophenyl) - 4% 2C4% 27% 2C5% 2C5% 27 -tetraphenyl - 1% 2C2% 27 -linked (ⅲ-imidazole) This substance is useful in many fields.
First, in the field of pharmaceutical research and development, its unique structure endows it with potential biological activity. It may act on specific biological targets and have exploratory value for the treatment of certain diseases. For example, it may be found to have growth inhibitory effects on specific cancer cells in research, or it may emerge in drug screening for neurodegenerative diseases, providing possible lead compounds for the creation of new drugs.
Second, in the field of materials science, due to the stable structure and special electronic properties of the compound, it may be used to prepare new photoelectric materials. For example, in the field of organic Light Emitting Diode (OLED), it can regulate the luminescence performance, improve the luminous efficiency and stability of the device; in solar cell materials, it may help to separate and transport photogenerated carriers, thereby improving the photoelectric conversion efficiency of the battery.
Third, in the field of catalysis, this compound may act as a ligand to coordinate with metal ions to form an efficient catalyst. It can be applied to organic synthesis reactions, such as carbon-carbon bond formation reactions, oxidation-reduction reactions, etc., to improve the selectivity and rate of the reaction, and to promote the development of green chemical synthesis.
Fourth, in the field of analysis and detection, due to its unique structure and properties, it can be used for the identification and detection of specific substances. For example, building chemical sensors that interact specifically with target analytes to achieve highly sensitive detection of environmental pollutants, biomarkers, etc.

2% 2C2% 27 -bis (o-chlorophenyl) - 4% 2C4% 27% 2C5% 2C5% 27 -tetraphenyl - 1% 2C2% 27 -linked (III-imidazole) This substance has unique physical and chemical properties. Looking at its state, it often takes the shape of [specific appearance], which is determined by its molecular structure arrangement. Its color, or [specific color], the appearance of this color, is related to the intramolecular electron transition.
On its melting point, it is about [specific melting point value]. When the temperature reaches this point, the intermolecular force weakens and the lattice structure begins to change. The boiling point is at [specific boiling point value], when the molecule obtains enough energy to break free from the liquid phase.
In terms of solubility, it is soluble in [specific solvent 1], because the solvent and the compound can form [specific interactions, such as hydrogen bonds, etc.]; in [specific solvent 2], it is difficult to dissolve, and the intermolecular forces between the two molecules do not match.
Stability is also an important property. Under normal conditions, it is quite stable and the molecular structure is not easy to change. In case of [specific conditions, such as high temperature, strong acid, etc.], it is easy to react, and the chemical bonds within the molecule are broken and rearranged, resulting in [specific reaction types and products]. The physical and chemical properties of this compound are closely related to its unique molecular structure, which lays the foundation for its application in various fields.

To prepare 2,2 '-bis (o-chlorophenyl) -4,4', 5,5 '-tetraphenyl-1,2' -biphenyl (ⅲ-imidazole), there are many methods, choose one or two.
Prepare o-chlorobenzaldehyde, acetophenone and other raw materials first. In a suitable reactor, put o-chlorobenzaldehyde and acetophenone, and use an appropriate amount of base as catalyst, such as sodium hydroxide or potassium hydroxide, in an alcohol solvent, heat it at controlled temperature to promote its condensation reaction. This process requires attention to temperature and reaction time to prevent side reactions from breeding. After the reaction is completed, the condensation product is obtained by conventional separation methods, such as extraction, distillation, etc.
Mix this product with an appropriate amount of imidazole derivatives in a specific solvent, such as dichloromethane or N, N-dimethylformamide. Add suitable catalysts, such as some transition metal salts, and react at a certain temperature. During this period, the reaction process can be closely monitored by means of thin-layer chromatography. After the reaction is completed, it is purified by column chromatography or recrystallization to obtain the target product 2,2 '-bis (o-chlorophenyl) -4,4', 5,5 '-tetraphenyl-1,2' -bis (ⅲ-imidazole).
Another method is to first react o-chlorophenzaldehyde with a specific amine compound to obtain a nitrogen-containing intermediate. After the intermediate is reacted with acetophenone derivative under suitable conditions, the target product can also be obtained through multi-step transformation. However, each method has its advantages and disadvantages, and the implementation needs to be weighed according to many factors such as raw material availability, cost, yield and so on.

I have not heard of the exact price of "2,2 '-bis (o-chlorophenyl) -4,4', 5,5 '-tetraphenyl-1,2' -imidazole (ⅲ-imidazole) " in the market. However, the price of this product may fluctuate greatly due to the difficulty of preparation, the variety of materials used, and the different uses.
If its preparation requires rare raw materials, or the process is complicated, requires precise instruments, strict temperature control, and takes a long time, the price will be high. And if it is used in niche and critical fields such as high-end scientific research and special pharmaceutical research and development, its price will also be high due to specific needs and small quantities.
On the contrary, if the preparation is becoming easier, the raw materials are easily available, and the application field is becoming more widespread and large-scale production, the price may decline.
In summary, the price range is difficult to determine in today's market. To know the exact price, it is necessary to consult chemical raw material suppliers, scientific research reagent sales offices and other professional places to obtain accurate prices.

2% 2C2% 27 - Bis% 28O - Chlorophenyl% 29 - 4% 2C4% 27% 2C5% 2C5% 27 - Tetraphenyl - 1% 2C2% 27 - Bi% 28III - Imidazole% 29 is an organic compound. The stability of this compound is related to its ability to maintain its own chemical structure and properties under different environments.
At room temperature and pressure without the influence of specific chemical reaction conditions, this compound may exhibit relative stability. Due to its molecular structure, each atom is connected to each other by chemical bonds to build a relatively stable structure. Among them, the interaction of structural units such as chlorophenyl, phenyl and imidazole rings may endow molecules with certain spatial resistance and electronic effects, which in turn contribute to their stability.
However, the stability is also affected by many external factors. In case of high temperature, the thermal motion of the molecule intensifies, the vibration of the chemical bond is enhanced, or the chemical bond is weakened or even broken, and the stability is reduced. If it is exposed to extreme high temperatures in a hot fire, the structure of the compound may be difficult to maintain.
Furthermore, specific chemical reagents will also affect its stability. Strong oxidizing agents or reducing agents can react with the compound and change its chemical structure. For example, when exposed to strong oxidants such as potassium permanganate, some chemical bonds in the compound may be oxidized, resulting in structural changes and impaired stability.
In addition, lighting conditions cannot be ignored. Some compounds are sensitive to light, and may cause luminescent chemical reactions under light. If the compound is sensitive to specific wavelengths of light, in the light environment, intra-molecular electrons excite, initiating chemical reactions, and stability is also affected.
In summary, the stability of 2% 2C2% 27 - Bis% 28O - Chlorophenyl% 29 - 4% 2C4% 27% 2C5% 2C5% 27 - Tetraphenyl - 1% 2C2% 27 - Bi% 28III - Imidazole% 29 is not static and often varies due to factors such as external temperature, chemical reagents, and light.