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What is the main use of 1H-Benzimidazole 2- [ (4-chlorophenyl) methyl]
1H-benzimidazole-2- [ (4-chlorophenyl) methyl] This substance has a wide range of uses. In the field of medicine, it is often the key raw material for the creation of new drugs. The genbenzimidazole structure plays an important role in many drug molecules, which can closely bind to specific targets in organisms and exhibit various biological activities, such as antibacterial, antiviral, and anti-tumor effects. The introduction of 4-chlorophenyl methyl may further optimize the pharmacological properties of drugs, such as enhancing its affinity for specific cells or pathogens, and enhancing the therapeutic effect.
In the field of materials science, it is also useful. It can be used as an important monomer in the synthesis of special functional materials. For example, by means of a specific chemical reaction, it is integrated into the structure of a polymer material, giving the material unique optical, electrical or thermal properties. Or participate in the construction of materials with special adsorption properties to enrich or separate specific substances, and play a role in environmental monitoring, chemical separation, etc.
In the agricultural field, it may contribute to the development of new pesticides. Because it has certain biological activity, it can be rationally designed and modified, or it can become an efficient, low-toxic and environmentally friendly pesticide ingredient to prevent and control pests and diseases, ensure the healthy growth of crops, and improve the efficiency of agricultural production. In short, 1H-benzimidazole-2- [ (4-chlorophenyl) methyl] has important potential application value in many fields, just like a shining gem, waiting for the world to dig deeper and make good use of it.
What are the physical properties of 1H-Benzimidazole 2- [ (4-chlorophenyl) methyl]
1H-benzimidazole-2- [ (4-chlorophenyl) methyl] This substance has important physical properties and is related to many uses. In terms of its properties, it is often crystalline, with a white appearance and pure texture, just like white jade carved, showing its pure state.
When it comes to melting point, this substance has a specific melting point value, about [X] degrees Celsius. The melting point is stable and accurate, like a nautical needle, providing a key basis for the identification and purification of this substance, like a beacon for navigators to guide the direction.
Solubility is also one of the key physical properties. In common organic solvents, such as ethanol, acetone, etc., it has a certain solubility. In ethanol, it is slightly soluble, just like snowflakes merging into a stream and slowly disappearing; in acetone, it has slightly better solubility, and can quickly blend with acetone to form a uniform system. This property makes it an important position in various chemical synthesis and preparation.
Furthermore, its density is also unique. After accurate measurement, the density is [X] grams per cubic centimeter. This value is like the weight of a substance, which determines its distribution and behavior in different environments. It is of great significance for practical application considerations, just like the accurate calculation of the weight of each brick when building a high-rise building. In addition, its stability is good, and under normal environmental conditions, it can maintain its own chemical structure and properties for a long time, just like an ancient city wall that has stood still after years of erosion. It is not easily disturbed by external factors, providing great convenience for its storage and transportation, and can be widely used in many fields without any worries.
What are the chemical properties of 1H-Benzimidazole 2- [ (4-chlorophenyl) methyl]
The chemical properties of 1H-benzimidazole-2- [ (4-chlorophenyl) methyl] are quite unique. In this compound, the part of 1H-benzimidazole has the characteristics of a nitrogen-containing heterocycle, and the nitrogen atom has lone pair electrons, so it can exhibit alkalinity and react with acids to form corresponding salts. At the same time, the heterocyclic structure endows the molecule with certain stability and aromaticity, which makes its electron cloud distribution show a special pattern and affects its chemical reactivity.
Furthermore, the chlorine atom in the 2 - [ (4-chlorophenyl) methyl] part, 4-chlorophenyl group, because of its large electronegativity, can change the electron cloud density of the benzene ring, resulting in a relatively low electron cloud density of the benzene ring o and para-site, which in turn affects the activity of the electrophilic substitution reaction and makes the reaction more likely to occur in the meta-site. The methylene connected to benzimidazole plays the role of connecting the two groups, and the hydrogen atom on the methylene group has a certain activity and can participate in some substitution reactions.
On the whole, 1H-benzimidazole-2- [ (4-chlorophenyl) methyl] has both the reactivity of nitrogen-containing heterocycles and the characteristics of chlorophenyl groups due to the interaction of these two parts. In the field of organic synthesis, it can be used as a key intermediate to construct more complex organic molecular structures and participate in many types of chemical reactions, such as nucleophilic substitution, electrophilic substitution, and reactions with metal-organic reagents. It exhibits diverse and important chemical properties and reactivity.
What is the production method of 1H-Benzimidazole 2- [ (4-chlorophenyl) methyl]
The preparation method of 1H-benzimidazole-2- [ (4-chlorophenyl) methyl] is involved in the field of organic synthesis. To prepare this product, the following steps are often followed.
The first step is to construct a benzimidazole skeleton with suitable starting materials. It can react with formic acid under specific conditions. The o-phenylenediamine and formic acid are mixed in a certain proportion, and in a heated environment, the two are condensed to form a benzimidazole structure. This reaction requires strict control of the temperature and reaction time. If the temperature is too high, or side reactions occur, the purity of the product decreases; if the reaction time is too short, the reaction is incomplete and the yield is not good. Generally speaking, the temperature is controlled between 100-150 ° C, and the reaction is appropriate for several hours.
Next step, introduce a (4-chlorophenyl) methyl group. The prepared benzimidazole is used as a substrate to react with a reagent containing (4-chlorophenyl) methyl. (4-chlorobenzyl) halides such as (4-chlorobenzyl) chloride or (4-chlorobenzyl) bromine are often used. In the presence of a base, the two undergo nucleophilic substitution. The function of the base is to capture the hydrogen on the benzimidazole nitrogen atom, enhance its nucleophilicity, and promote the smooth progress of the reaction. Commonly used bases include potassium carbonate, sodium carbonate, etc. The reaction is carried out in organic solvents, such as N, N-dimethylformamide (DMF), dimethyl sulfoxide (DMSO), etc. Such solvents can effectively dissolve the reactants and facilitate full contact of the reaction. The reaction temperature is usually controlled at 50-100 ° C, and the reaction time depends on the specific situation, generally 6-12 hours.
After the reaction is completed, the product needs to be separated and purified. The commonly used method is column chromatography, using silica gel as the fixed phase, and selecting a suitable eluent, such as a mixed solvent of petroleum ether and ethyl acetate, to achieve separation according to the difference between the polarity of the product and the impurity. The recrystallization method can also be used to select a suitable solvent to dissolve the product, cool and crystallize to obtain high-purity 1H-benzimidazole-2 - [ (4-chlorophenyl) methyl]. In this way, the target product can be obtained through a series of operations.
What is the price range of 1H-Benzimidazole 2- [ (4-chlorophenyl) methyl] in the market?
1H-benzimidazole-2- [ (4-chlorophenyl) methyl] This product is in the market, and its price range is difficult to break. Its price is not static, but often changes due to many reasons.
Its price may vary due to the simplicity of the production method. If the preparation method is exquisite and complicated, requires many processes, rare drugs, and has strict requirements on appliances and the environment, the cost will be high, and the price will be high. On the contrary, if the production method is simple, the required materials are easy to obtain, the cost will decrease, and the price will also decrease.
Furthermore, the supply and demand of the market is also the key. If this product is widely needed and has a wide range of uses, such as medicine, chemical industry and many other fields, and the supply is relatively scarce, the price will rise. However, if the market is oversupplied, merchants may reduce prices to promote transactions in order to sell their goods.
In addition, the price of raw materials also affects. If the price of raw materials required for production, such as 4-chlorophenyl, fluctuates due to factors such as origin, season, and output, the price of 1H-benzimidazole-2 - [ (4-chlorophenyl) methyl] will also change accordingly.
Overall, the price range is difficult to determine, either as low as a few dollars, or as high as a hundred gold, depending on the above factors.