Chemical Formula | C14H10ClFN2 |
Molecular Weight | 260.698 g/mol |
Appearance | Typically a solid (description may vary by purity and conditions) |
Melting Point | Data may vary based on purity and experimental conditions |
Boiling Point | Specific value depends on purity and experimental setup |
Solubility In Organic Solvents | Soluble in some common organic solvents like dichloromethane, chloroform |
Density | Data may be lacking or vary based on form and purity |
Pka | Related to the acid - base properties of the benzimidazole moiety, specific value depends on environment |
Logp | Indicates lipophilicity, value reflects its tendency to partition between octanol and water |
Chemical Formula | C14H10ClFN2 |
Molar Mass | 260.696 g/mol |
Appearance | Solid (predicted) |
What are the chemical properties of 2-Chloro-1- (4-fluorobenzyl) benzimidazole?
2-Chloro-1- (4-fluorobenzyl) benzimidazole, an organic compound. Its chemical properties are of great interest and have attracted the attention of many chemistry researchers.
Looking at its structure, the benzimidazole ring system is very stable, which is the core structure of this compound. The introduction of the 2-position chlorine atom endows it with a certain chemical activity. The chlorine atom has electron-absorbing properties, which can affect the distribution of electron clouds on the benzimidazole ring, and then change the reactivity of each atom on the ring. In the nucleophilic substitution reaction, the chlorine atom can react with the nucleophilic reagent as a leaving group to derive a series of new compounds. < Br >
Furthermore, the 1-linked (4-fluorobenzyl) group is also significant. The electronegativity of fluorine atoms is quite high, and its existence will affect the electron cloud density of the benzyl part. At the same time, the carbon-carbon bond of the benzyl part is relatively stable, but the hydrogen atom on its α-carbon can participate in the reaction under certain conditions, such as oxidation reaction or nucleophilic substitution reaction, because the intermediate of benzyl carbon cation is relatively stable.
In terms of physical properties, this compound is usually in a solid state due to the existence of van der Waals forces and possible hydrogen bond interactions between molecules. Its solubility is related to the polarity of the molecule. The benzimidazole ring, chlorine atom and fluorine atom all affect the polarity of the molecule. Generally, there is a certain solubility in organic solvents such as dichloromethane and chloroform, but the solubility in water is relatively low. Because water is a strong polar solvent, the interaction with the compound molecules is weak.
In terms of chemical reactivity, in addition to the above-mentioned nucleophilic substitution reaction, the nitrogen atom of the benzimidazole ring can be used as a nucleophilic check point to react with electrophilic reagents. For example, by reacting with acyl halides or haloalkanes, new substituents are introduced on the nitrogen atom, thereby expanding the chemical derivation path of the compound and laying the foundation for the synthesis of compounds with more complex structures.
What are the physical properties of 2-Chloro-1- (4-fluorobenzyl) benzimidazole
2-Chloro-1- (4-fluorobenzyl) benzimidazole is one of the organic compounds. Its physical properties are very important and are related to many characteristics of this compound.
This compound may be in a solid state at room temperature, and its texture may be crystalline. Looking at its color, it may be white to off-white, and its color is relatively pure. Its melting point is one of the key physical parameters, usually around a specific temperature range. This temperature range makes this substance change from solid to liquid. In chemical research and practical applications, knowing the melting point helps to control its phase change.
In terms of solubility, 2-chloro-1- (4-fluorobenzyl) benzimidazole has different manifestations in organic solvents. In common organic solvents, such as ethanol and dichloromethane, it has a certain solubility, which makes it easy to participate in the reaction in the form of solution in the process of organic synthesis, providing convenience for the design of synthesis routes. However, in water, its solubility is very small, because the molecular structure of the compound is composed of carbon, hydrogen, nitrogen, chlorine, fluorine and other elements, the polarity is weak, and the force between it and water molecules is small, so it is difficult to dissolve in water.
Furthermore, its density is also one of the physical properties. Although the exact value varies slightly due to the measurement conditions, its density is relatively fixed. This parameter is indispensable in the study of mass and volume conversion, or the distribution of substances in a specific system.
In addition, the stability of this compound also belongs to the category of physical properties. Under general environmental conditions, 2-chloro-1- (4-fluorobenzyl) benzimidazole is relatively stable, but under extreme conditions such as high temperature and strong oxidants, its structure may change, which affects its chemical properties and applications.
In summary, the physical properties of 2-chloro-1- (4-fluorobenzyl) benzimidazole, such as state, color, melting point, solubility, density, and stability, are of great significance for its applications in chemical research, drug synthesis, materials science, and other fields. Researchers need to understand in detail in order to make good use of this compound.
What is the preparation method of 2-Chloro-1- (4-fluorobenzyl) benzimidazole
The preparation of 2-chloro-1- (4-fluorobenzyl) benzimidazole is an important technique in the field of chemical synthesis. To prepare this substance, the common method is to use an appropriate starting material through a series of carefully designed chemical reaction steps.
First, the appropriate starting reactant needs to be selected. Generally speaking, the starting material containing benzimidazole structure and related compounds containing 4-fluorobenzyl and chlorine substituents will be selected. The purity and quality of the starting material have a great influence on the quality of the final product, so it needs to be strictly controlled.
Later, the common reaction types in organic synthesis are often used. For example, the nucleophilic substitution reaction can be used to make the compound containing benzimidazole structure interact with the halogenated benzyl structure. During the reaction process, the control of the reaction conditions is crucial, such as the reaction temperature, reaction time, molar ratio of the reactants, and the choice of solvent and catalyst, all of which will have a significant impact on the reaction process and the yield of the product.
The reaction temperature needs to be precisely controlled according to the activity of the reactants involved and the reaction mechanism. If the temperature is too high, it may increase the side reaction and decrease the purity of the product; if the temperature is too low, the reaction rate will be delayed and take a long time. The reaction time also needs to be properly controlled. If it is too short, the reaction will not be fully functional, and it will be too long or cause unnecessary side reactions. The molar ratio of the
reactants is also an important consideration. The appropriate ratio can promote the smooth progress of the reaction in the direction of generating the target product and improve the yield of the product. The choice of solvent depends on the solubility and reactivity of the reactants, and the reaction rate and selectivity may vary in different solvents. The addition of catalysts can often accelerate the reaction process, reduce the activation energy of the reaction, and improve the reaction efficiency.
After the reaction is completed, the separation and purification steps are required to obtain high-purity 2-chloro-1 - (4-fluorobenzyl) benzimidazole. Commonly used separation methods include extraction, distillation, column chromatography, etc. According to the physical and chemical properties of the product and impurities, an appropriate method is selected to achieve the purpose of purifying the product.
In which fields is 2-Chloro-1- (4-fluorobenzyl) benzimidazole used?
2-Chloro-1- (4-fluorobenzyl) benzimidazole is an organic compound that is used in many fields.
In the field of medicine, it can be used as an intermediate for drug synthesis. Due to its special chemical structure, it can react with other compounds by organic synthesis to prepare drugs with specific pharmacological activities. Or it can participate in the synthesis of anti-parasitic drugs, and the modified structure can make it inhibit or kill specific parasites to help treat parasite-related diseases.
In the field of materials science, it may be used to create new polymer materials. Because of its stable structure and certain reactivity, it can be used as a monomer or crosslinking agent for polymerization reaction. By polymerizing with other monomers, the material can be endowed with unique properties, such as enhancing the heat resistance and mechanical strength of the material, or endowing it with special optical and electrical properties, which have potential application value in electronic devices, aerospace and other fields.
In agriculture, it may be developed as a pesticide. Due to its chemical properties, it may have a control effect on diseases and pests of some crops. It may interfere with the physiological and metabolic processes of pests, or inhibit the growth and reproduction of certain pathogenic bacteria, so as to protect the healthy growth of crops and improve the yield and quality of crops.
In the field of scientific research and exploration, this compound is often used as a research object due to its unique structure, helping scientists gain in-depth insight into the mechanism of organic chemical reactions. By studying its reaction characteristics, the methods and strategies of organic synthesis can be expanded, laying the foundation for the creation of new compounds and the development of new materials.
What is the market outlook for 2-Chloro-1- (4-fluorobenzyl) benzimidazole?
2-Chloro-1- (4-fluorobenzyl) benzimidazole, this is an organic compound. In terms of current market prospects, it has emerged in the field of medicine and pesticides and has great potential for development.
Looking at the field of medicine, with the progress of scientific research, the research on various disease targets continues to deepen. Numerous studies have shown that benzimidazole compounds have potential therapeutic effects on specific diseases. 2-Chloro-1- (4-fluorobenzyl) benzimidazole has a unique structure and can interact with specific biomacromolecules, thereby exhibiting pharmacological activities such as antibacterial, antiviral, and antitumor. In recent years, the research and development of anti-tumor drugs has attracted much attention. Due to its unique structure, this compound is expected to become the lead compound of new anti-tumor drugs. Researchers have modified and optimized its structure, hoping to improve the efficacy and reduce toxic and side effects. Therefore, in the frontier field of pharmaceutical research and development, its market demand may increase with the deepening of research.
In the field of pesticides, the resistance of pests to traditional pesticides is increasing, and the research and development of new pesticides is imminent. 2-Chloro-1- (4-fluorobenzyl) benzimidazole may have a unique insecticidal and bactericidal mechanism, which can have an effect against pests and bacteria. With the increasing emphasis on the quality and safety of agricultural products and environmental protection, the demand for high-efficiency, low-toxicity and environmentally friendly pesticides is strong. If this compound can meet these requirements, it will gain broad space in the pesticide market, whether it is used for field crops, or for pest control of cash crops such as vegetables and fruits, it has potential application prospects.
However, its market expansion also faces challenges. The synthesis process needs to be further optimized to reduce production costs, improve yield and purity, so as to enhance market competitiveness. And new drugs and new pesticides have a long R & D cycle and huge investment, and need to pass strict safety and effectiveness evaluations. However, overall, with the potential application value in the field of medicine and pesticides, the market prospect of 2-chloro-1- (4-fluorobenzyl) benzimidazole is relatively optimistic, and it is expected to occupy an important position in the future development of related industries.