1h Benzimidazole 6 Carboxylic Acid 5 4 Bromo 2 Chlorophenyl Amino 4 Fluoro 1 Methyl Methyl Ester
quinoline thiophene imidazole thiazole

1H-Benzimidazole-6-carboxylic acid,5-[(4-bromo-2-chlorophenyl)amino]-4-fluoro-1-methyl-, methyl ester

    Specifications

    HS Code

    748472

    Chemical Formula C16H12BrClFN3O2
    Molecular Weight 412.64
    Appearance Unknown
    Melting Point Unknown
    Boiling Point Unknown
    Solubility In Water Unknown
    Solubility In Organic Solvents Unknown
    Density Unknown
    Flash Point Unknown
    Pka Unknown

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    General Information
    Where to Buy 1H-Benzimidazole-6-carboxylic acid,5-[(4-bromo-2-chlorophenyl)amino]-4-fluoro-1-methyl-, methyl ester in China?
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    Frequently Asked Questions

    As a leading 1H-Benzimidazole-6-carboxylic acid,5-[(4-bromo-2-chlorophenyl)amino]-4-fluoro-1-methyl-, methyl ester supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

    What is the chemical structure of 1H-Benzimidazole-6-carboxylic acid, 5- [ (4-bromo-2-chlorophenyl) amino] -4-fluoro-1-methyl-, methyl ester?
    The chemical structure of 1H-benzimidazole-6-carboxylic acid, 5- [ (4-bromo-2-chlorophenyl) amino] -4-fluoro-1-methyl-, methyl ester is a complex and delicate structure in the field of organic chemistry. This compound is based on the benzimidazole parent nucleus, which is connected with a variety of substituents at specific positions.
    The benzimidazole parent nucleus has a nitrogen-containing heterocyclic structure with unique electron cloud distribution and chemical activity. The 6-position is connected with a carboxyl group and exists in the form of a methyl ester. The -COOCH 🥰 structure endows the molecule with certain lipophilicity and reactivity. The 5-position is connected to 4-bromo-2-chlorophenyl via amino group, and the introduction of bromine and chlorine atoms changes the electron cloud density of the benzene ring, which affects the molecular polarity, reaction check point and biological activity. The introduction of fluorine atoms at the 4-position further adjusts the electronic structure of the molecule due to the large electronegativity of fluorine atoms, which affects its physicochemical properties and biological activities. The substitution of methyl at the 1-position changes the steric resistance and lipophilicity of the molecule.
    Overall, the interaction between atoms and groups in this chemical structure synergistically determines the unique physicochemical properties and potential biological activities of the compound. It may have important research value and application potential in the fields of medicinal chemistry, organic synthesis chemistry and other fields.
    What are the physical properties of 1H-Benzimidazole-6-carboxylic acid, 5- [ (4-bromo-2-chlorophenyl) amino] -4-fluoro-1-methyl-, methyl ester?
    1H-benzimidazole-6-carboxylic acid, 5- [ (4-bromo-2-chlorophenyl) amino] -4-fluoro-1-methyl -, methyl ester, its physical properties are quite complex. Looking at its morphology, it may be solid at room temperature, but the exact state depends on the preparation process and environmental conditions. When it comes to color, or white to light yellow powder, just like late autumn frost, the color is light and elegant.
    As for the melting point, determined by fine experiments, it is about a specific temperature range. This temperature range is crucial for its identification and purity determination. It is like a precise scale that defines its characteristics. Its solubility is also a key property. In organic solvents, it may behave differently. In some organic solvents, such as dichloromethane, N, N-dimethylformamide, etc., it may have a certain solubility, like fish entering water, it can be moderately melted; in water, the solubility may be very low, like oil floating in water, and it is difficult to miscible.
    Furthermore, density is also a physical property that cannot be ignored. Although the exact value needs to be measured by professional instruments, the characteristics of its relative density are instructive in the separation, purification and selection of application scenarios of substances, just like the rudder of a ship, guiding the direction. Its stability may be relatively good in normal environments, but it may change in case of high temperature, strong light or specific chemical substances, just like a delicate flower meeting a strong wind, and its shape is easy to change. These many physical properties are interrelated, and together outline the physical outline of the substance, laying the foundation for its application in scientific research, industry and other fields.
    What are the main uses of 1H-Benzimidazole-6-carboxylic acid, 5- [ (4-bromo-2-chlorophenyl) amino] -4-fluoro-1-methyl-, methyl ester?
    1H-benzimidazole-6-carboxylic acid, 5- [ (4-bromo-2-chlorophenyl) amino] -4-fluoro-1-methyl-, methyl ester. Its use is quite specific, but it is difficult to find it in ancient books. Today, it is speculative.
    Or used in medicine. Looking at its chemical structure, it is fine and unique, or it is helpful for the development of new drugs. Nowadays, medicine is often based on chemically synthesized materials to develop remedies for treating diseases and saving people. The structure of this substance is complex, or it can be targeted at the target of specific diseases. After pharmacological research and experiments, it can be made into a drug to cure diseases, such as fighting tumors and relieving inflammation.
    Or it can be used in the field of materials science. Modern materials pursue high performance and multi-functionality, and chemical compounds are often the key elements. This methyl ester may be used as a special additive to be incorporated into specific materials to improve the properties of materials. Such as enhancing the stability of materials and improving their optical properties, making materials suitable for high-end fields such as optical instruments and electronic components.
    In addition, the road of scientific research and exploration may also need its help. In the research of organic synthetic chemistry, it may serve as a key intermediate. By reacting and transforming them, chemists have derived more compounds with novel structures, expanding the boundaries of organic chemistry and paving the way for future scientific and technological progress. Although it is difficult to determine its true use, according to the current trend of scientific development, there may be one of the above uses.
    What are the synthesis methods of 1H-Benzimidazole-6-carboxylic acid, 5- [ (4-bromo-2-chlorophenyl) amino] -4-fluoro-1-methyl-, methyl ester?
    The synthesis method of 1H-benzimidazole-6-carboxylic acid, 5- [ (4-bromo-2-chlorophenyl) amino] -4-fluoro-1-methyl-methyl-methyl ester is complicated, and it is described in detail today.
    First, the starting material can be halogenated to obtain a halogen containing bromine and chlorine. Select a suitable halogenating reagent, and at a suitable temperature and reaction time, the halogen atom can be precisely introduced into the target check point. This step requires controlling the reaction conditions to prevent side reactions from generating and causing the product to be impure.
    Second, the fluorine-containing, methyl-containing benzimidazole derivatives are connected to the above-mentioned halides by a condensation reaction. Select a condensation agent with suitable activity, and with the help of a catalyst, promote the combination of the two. In this process, the choice of solvent is also critical, and it is necessary to consider its influence on the solubility and reactivity of the reactants.
    Furthermore, the ester-forming reaction is necessary to obtain methyl esters. Take the intermediate obtained from the reaction and esterify it with methanol under acid or base catalysis. When acid catalysis is used, strong acids such as sulfuric acid are commonly used; when alkali catalysis is used, the type and dosage of bases need to be precisely controlled to obtain high-yield methyl ester products.
    In addition, during the reaction process, monitoring methods are indispensable. Thin-layer chromatography and high-performance liquid chromatography can be used to observe the progress of the reaction and determine the end point of the reaction, so as to adjust the reaction conditions in time. The product is separated and purified by column chromatography, recrystallization and other methods to remove impurities to obtain pure 1H-benzimidazole-6-carboxylic acid, 5- [ (4-bromo-2-chlorophenyl) amino] -4-fluoro-1-methyl -, methyl ester, in order to meet the needs of experiments and applications.
    1H-Benzimidazole-6-carboxylic acid, 5- [ (4-bromo-2-chlorophenyl) amino] -4-fluoro-1-methyl-, methyl ester market prospects?
    Today, there are 1H-benzimidazole-6-carboxylic acid, 5- [ (4-bromo-2-chlorophenyl) amino] -4-fluoro-1-methyl-methyl-methyl ester, and its market prospects have attracted much attention. If we look at it from an ancient method, we can only know its clues when we look at the four things carefully.
    Looking at the world's pharmaceutical chemical market, it has developed rapidly in recent years, and all kinds of new drug research and development have emerged one after another. This 1H-benzimidazole derivative may have potential uses in the field of medicine due to its unique molecular structure. Today, many pharmaceutical companies are competing to explore new active pharmaceutical ingredients to solve the suffering of patients in the world. If this compound is effective in treating certain diseases, it will definitely stimulate the market.
    Let's talk about the chemical raw material market, the supply and price fluctuations of raw materials have a profound impact on its production. 4-Bromo-2-chloroaniline, 1-methyl-4-fluoro-1H-benzimidazole-6-carboxylic acid methyl ester and other raw materials, if the supply is stable and the price is suitable, can pave the way for its large-scale production. On the contrary, if the supply of raw materials is in short supply or the price rises sharply, the production cost will increase greatly and the market expansion will also be hindered.
    Furthermore, the state of peer competition cannot be ignored. There are many chemical pharmaceutical companies in the world, or there are already peers in the industry who have glimpsed the potential of this compound and are the first to lay out R & D and production. If they do not have their own unique process and cost advantages, it may be difficult to win a place in the market.
    However, if they can make good use of the right time and the right place, find the unique application of this compound, optimize the production process, and control the cost, they may be able to emerge in the market, achieve some achievements, and leave a good name in the field of pharmaceutical and chemical industry, and also seek well-being for the people of the world.