5 Trifluoromethyl 1h Benzimidazole 2 Carboxylic Acid
quinoline thiophene imidazole thiazole

5-(Trifluoromethyl)-1H-benzimidazole-2-carboxylic acid

    Specifications

    HS Code

    224927

    Chemical Formula C9H5F3N2O2
    Molecular Weight 230.14
    Appearance Solid (likely white or off - white powder)
    Solubility In Water Low (due to the non - polar trifluoromethyl and benzimidazole groups)
    Solubility In Organic Solvents Soluble in polar organic solvents like DMSO, DMF; less soluble in non - polar solvents
    Pka Carboxylic Acid Group Typical range for aromatic carboxylic acids around 3 - 5
    Uv Vis Absorption Absorption bands characteristic of the benzimidazole ring and the influence of the trifluoromethyl group

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    General Information
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    Frequently Asked Questions

    As a leading 5-(Trifluoromethyl)-1H-benzimidazole-2-carboxylic acid 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 chemical properties of 5- (trifluoromethyl) -1H-benzimidazole-2-carboxylic acid?
    5- (trifluoromethyl) -1H-indole-2-carboxylic acid is an organic compound. It is acidic, and the carboxyl group can be released as a proton. It acts as an acid in the acid-base reaction and forms a salt with the base. This compound contains an indole ring, which is aromatic and has high stability. It can participate in electrophilic substitution reactions, such as halogenation, nitrification, sulfonation, etc. Electrophilic reagents attack the high electron cloud density area of the indole ring. Because of its trifluoromethyl group, this group has strong electron absorption, which affects the electron cloud distribution and reactivity of the compound, enhances the acidity of the carboxyl group, and also affects the molecular polarity and fat solubility, which in turn affects its physicochemical properties and biological activities At the same time, the indole ring of this compound can participate in a variety of heterocyclic synthesis reactions. With appropriate reaction conditions and reagents, heterocyclic compounds with complex and diverse structures can be constructed, which are widely used in the fields of organic synthesis and medicinal chemistry, laying the foundation for the creation of new compounds with specific biological activities and pharmacological properties.
    What are the synthesis methods of 5- (trifluoromethyl) -1H-benzimidazole-2-carboxylic acid?
    The synthesis method of 5- (trifluoromethyl) -1H-benzimidazole-2-carboxylic acid has been around for a long time, and many paths have been developed with the change of years.
    First, it uses o-phenylenediamine and trifluoroacetic acid or its derivatives as starting materials. Under suitable reaction conditions, the two can be condensed and cyclized to obtain the target product. The raw materials of this method are relatively common, but the control of the reaction conditions needs to be fine, otherwise it is easy to produce side reactions, resulting in the purity and yield of the product being affected.
    Second, through the conversion of nitroaromatic hydrocarbons. First, the aromatic hydrocarbon compound containing nitro group is reduced to obtain the corresponding amine, and then reacts with the trifluoroacetyl compound, and then forms a ring through cyclization reaction. This path has a little more steps, but the selectivity of the raw material is wide, and the reaction conditions can be flexibly adjusted according to the characteristics of different starting materials to achieve the desired effect.
    Third, halogenated aromatic hydrocarbons are used as starting materials. The halogenated aromatic hydrocarbons and the reagents containing trifluoromethyl groups are coupled under the action of catalysts, and then the product is prepared by subsequent cyclization reaction. This method relies on efficient catalysts, which require high reaction equipment and operation. However, if used properly, the target product can be synthesized efficiently, and the product structure is easy to control.
    Each of these methods has its own advantages and disadvantages, and it is necessary to comprehensively consider the actual situation, such as the availability of raw materials, reaction cost, product purity requirements, etc., and carefully choose to achieve the ideal synthesis effect.
    In which fields are 5- (trifluoromethyl) -1H-benzimidazole-2-carboxylic acids used?
    5- (triethylmethyl) -1H-benzimidazole-2-carboxylic acid, which is useful in many fields such as medicine and chemical industry.
    In the field of medicine, it is often used as a key intermediate in drug synthesis. The structure of Geiinbenzimidazole has unique biological activities, and this structure can be modified to obtain compounds with various pharmacological properties. For example, by chemically modifying 5- (triethylmethyl) -1H-benzimidazole-2-carboxylic acid, drugs with antibacterial activity can be prepared, which can effectively inhibit bacterial growth and reproduction, and contribute to the development of anti-infective drugs; drugs with anti-tumor activity can also be prepared, which act on specific targets of tumor cells, or block tumor cell proliferation signaling pathways, or induce tumor cell apoptosis, opening up new paths for the development of tumor therapeutic drugs.
    In the chemical field, it has outstanding performance in material synthesis. It can be used as a monomer for synthesizing functional polymer materials, giving materials special properties. If it is introduced into polymer, it can improve the thermal stability of the material, so that the material can still maintain good physical and chemical properties in high temperature environment, and is widely used in aerospace, electronic appliances and other fields that require strict thermal stability of materials; or enhance the adsorption performance of the material, so that the material has a strong adsorption force for specific substances, and can play a role in sewage treatment, gas purification and other fields. It can efficiently remove heavy metal ions, organic pollutants in sewage, or purify harmful gases in the air.
    In summary, 5- (triethylmethyl) -1H-benzimidazole-2-carboxylic acid plays an important role in the field of medicine and chemical industry due to its unique structure and properties, providing strong support for the development of related industries.
    What is the market price of 5- (trifluoromethyl) -1H-benzimidazole-2-carboxylic acid?
    Today there are 5- (trifluoromethyl) -1H -benzimidazole-2 -carboxylic acids, and their market price depends on many reasons. This compound is used in various fields such as medicine, pesticides and materials, and the amount of demand has a huge impact on its price. If the demand for this substance surges when developing new drugs, the price may rise; if the development of related industries slows down, the demand may fall, and the price may also fall.
    And the preparation method and cost are also the main reasons for pricing. If the preparation process is complicated, the materials used are expensive, and high-end equipment and fine operation are required, the cost will be high, and the price will also be high; if there is a simple and low-cost preparation method, the price may drop.
    The supply of raw materials also affects its price. If raw materials are scarce, or the supply is not smooth due to natural disasters in the place of origin, geopolitics, etc., the price will increase; if raw materials are abundant, the supply will be stable, and the price will be stable or reduced.
    Furthermore, the situation of market competition also has a great impact on its price. If there are many merchants and the competition is intense, they may have a price reduction strategy in order to occupy the market; if there are few merchants and they have a monopoly, the price may be high.
    In short, the market price of 5- (trifluoromethyl) -1H-benzimidazole-2-carboxylic acid is constantly changing due to the interaction of many factors such as demand, preparation cost, raw material supply and market competition. To know the real-time price, you need to carefully observe the market dynamics and consult industry experts or relevant trading platforms.
    What are the precautions in the preparation of 5- (trifluoromethyl) -1H-benzimidazole-2-carboxylic acid?
    There are many precautions in the preparation of 5- (trifluoromethyl) -1H -indole-2-carboxylic acid.
    First, the selection of raw materials must be accurate. The quality and purity of the starting materials used are related to the success or failure of the product. Impurities exist in the raw materials, which are prone to side reactions and reduce the purity and yield of the product. It is necessary to strictly control the source of raw materials and carefully test the purity.
    Second, the reaction conditions are harsh. Temperature, pH, reaction time, etc. are all critical. Improper temperature may make the reaction too slow and incomplete, or cause the reaction to overreact and produce impurities. If some steps are sensitive to temperature, with slight deviations, the products are very different. The pH also affects the reaction process and direction. A specific reaction requires a specific pH environment to promote the positive progress of the reaction. If the reaction time is insufficient, it is difficult to fully convert the raw materials; if it is too long, it may cause side reactions.
    Third, choose the solvent carefully. The solvent not only dissolves the reactants, but also affects the reaction rate and selectivity. Different solvents have different polarities and solubility, which have different effects on the reaction. The choice of solvent needs to integrate the characteristics of the reactants and products and the reaction mechanism to ensure a smooth reaction.
    Fourth, the operation process is fine. Details such as the feeding sequence and stirring speed should not be taken lightly. The wrong feeding sequence may trigger a sudden reaction, endangering safety. Uneven stirring, uneven contact of the reactants, and difficulty in synchronizing the reaction affect the yield and quality. < Br >
    Fifth, separation and purification is exquisite. After the reaction is completed, the product is often mixed with impurities, and suitable separation and purification methods are required. Extraction, distillation, recrystallization and other methods have their own scope and limitations. Choose the right method and operate reasonably to obtain high-purity products. Slightly poor pools, impurity residue, affect the properties of the product.