4 Difluoromethyl 2 Methyl Thiazole 5 Carboxylic Acid
quinoline thiophene imidazole thiazole

4-Difluoromethyl-2-methyl-thiazole-5-carboxylic acid

    Specifications

    HS Code

    511947

    Name 4-Difluoromethyl-2-methyl-thiazole-5-carboxylic acid
    Chemical Formula C6H5F2NOS
    Molar Mass 179.172 g/mol
    Appearance Solid (usually)
    Solubility In Water Low solubility (organic acid with non - polar groups)
    Solubility In Organic Solvents Soluble in some polar organic solvents like DMSO, DMF

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    General Information
    Where to Buy 4-Difluoromethyl-2-methyl-thiazole-5-carboxylic acid in China?
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    Frequently Asked Questions

    As a leading 4-Difluoromethyl-2-methyl-thiazole-5-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 is the chemistry of 4-Difluoromethyl-2-methyl-thiazole-5-carboxylic acid?
    4-Difluoromethyl-2-methyl-thiazole-5-carboxylic acid is also an organic compound. Its molecular structure is unique, with a thiazole ring as the base, and the ring is connected with difluoromethyl, methyl and carboxyl groups. This compound has specific chemical properties and is very important in the field of organic synthesis.
    In terms of its chemical activity, the carboxyl group is acidic and can participate in acid-base reactions. It can react with bases to form salts. And the carboxyl group can be esterified and combined with alcohols to form ester compounds, which are commonly used in organic synthesis of ester products. The introduction of
    difluoromethyl greatly affects the physical and chemical properties of the compound. The electronegativity of fluorine atom is extremely high, and difluoromethyl can change the polarity of the molecule, affecting its solubility and reactivity. The special electronic effect of fluorine atom can affect the electron cloud density distribution of thiazole ring, which in turn affects the chemical reactivity and selectivity on the ring.
    2-methyl is based on the thiazole ring and also has an effect on the molecular properties. Methyl is the power supply, which can increase the electron cloud density of the thiazole ring and change its electrophilic and nucleophilic reactivity.
    The stability of this compound depends on its molecular structure. The thiazole ring has certain aromaticity and endows the molecule with certain stability. However, under certain conditions, such as high temperature, strong acid, strong base or strong oxidant, its structure may be damaged, causing chemical reactions to occur and molecular conversion into other compounds.
    In short, 4-difluoromethyl-2-methyl-thiazole-5-carboxylic acid has potential application value in many fields such as organic synthesis and pharmaceutical chemistry due to its unique structure and diverse chemical properties.
    What are the main uses of 4-Difluoromethyl-2-methyl-thiazole-5-carboxylic acid?
    4-Difluoromethyl-2-methyl-thiazole-5-carboxylic acid, which has a wide range of uses, is a key raw material for the synthesis of specific drugs in the field of medicinal chemistry. It can participate in the construction of molecular structures with unique biological activities, which is of great help to the research and development of new antibacterial and anti-inflammatory drugs. The characteristics of Gainthiazole ring and fluorine-containing groups can enhance the binding force between drugs and targets and improve the efficacy.
    In the field of pesticide chemistry, it is also indispensable. It can be used as a starting material for the creation of high-efficiency and low-toxicity pesticides. By modifying its structure, pesticide varieties with high selectivity to pests, strong lethality and environmental friendliness can be derived, which contributes to the sustainable development of agriculture.
    In the field of materials science, it has also made a name for itself. It can be introduced into polymer materials through specific reactions, endowing the materials with excellent properties such as weather resistance and chemical corrosion resistance, thereby expanding the application scenarios of materials, and may have outstanding performance in high-end fields such as aerospace and automobile manufacturing. In short, 4-difluoromethyl-2-methyl-thiazole-5-carboxylic acid plays an important role in many fields due to its unique structure and properties, and has broad prospects.
    What are the synthetic methods of 4-Difluoromethyl-2-methyl-thiazole-5-carboxylic acid?
    There are several common methods for the synthesis of Fu 4-difluoromethyl-2-methyl-thiazole-5-carboxylic acid. First, a difluoromethyl group can be introduced by a specific halogenation reaction starting from the starting material containing the thiazole ring. In this process, suitable halogenating reagents, such as fluorine-containing halides, need to be selected, and the reaction conditions, such as temperature, reaction duration, and molar ratio of the reactants, need to be finely regulated. If the temperature is too high or too low, the reaction may be biased towards side reactions, or the reaction rate is too slow, which affects the yield.
    Furthermore, the target product is obtained by difluoromethylation with 2-methyl-thiazole-5-carboxylic acid as the base. Among them, the choice of difluoromethylation reagents is particularly critical, and specific organic reagents with high reactivity can be selected. At the same time, the nature of the reaction solvent needs to be considered. Polar or non-polar solvents have a great influence on the reaction process and product purity. In polar solvents, some reagents have better solubility and may be easier to react, but may also cause unnecessary side reactions.
    In addition, there are strategies to introduce difluoromethyl and methyl at the same time to construct thiazole rings. The intermediate containing the corresponding functional group is first prepared by multi-step reaction, and then cyclized to form a thiazole ring. Although this approach is slightly complicated, each functional group can be precisely controlled in the early stage, thereby improving the selectivity of the target product. After each step of reaction, the product needs to be properly separated and purified to remove impurities and ensure the smooth follow-up reaction. For example, high-purity intermediates are obtained by extraction, column chromatography, etc., and then the cyclization conditions are optimized to obtain 4-difluoromethyl-2-methyl-thiazole-5-carboxylic acid.
    What is the price range of 4-Difluoromethyl-2-methyl-thiazole-5-carboxylic acid in the market?
    Today there is 4-difluoromethyl-2-methyl-thiazole-5-carboxylic acid, and I would like to know its price range on the market. However, after checking all the records in Tiangong Kaiwu in the past, the exact price of this product cannot be obtained. Because Tiangong Kaiwu is an ancient scientific and technological work, most of the products and processes recorded at that time were common. The fine substances of this chemical synthesis are not available in its era, so there is no way to obtain the price according to this book.
    The price of this product at present depends on many factors. First, the complexity of its preparation process, if the preparation requires delicate steps, special raw materials and equipment, the cost will be high, and the price will be high; second, the market supply and demand situation, if there are many people and few suppliers, the price will be high, otherwise the price will be low; third, the quality grade difference, high purity, high quality price is higher than ordinary.
    Although there is no "Tiangong Kaiwu" basis, you can consult the chemical raw material trading market, relevant manufacturers or chemical reagent suppliers, and you can also check industry reports and market survey data to understand the current price range of 4-difluoromethyl-2-methyl-thiazole-5-carboxylic acid.
    4-Difluoromethyl-2-methyl-thiazole-5-carboxylic acid is safe and toxic
    4-Difluoromethyl-2-methyl-thiazole-5-carboxylic acid, this is an organic compound. When exploring its safety and toxicity, it is necessary to consider many aspects.
    Looking at its chemical structure, thiazole ring is connected to difluoromethyl, methyl and carboxyl groups. In such structures, the introduction of fluorine atoms often changes the physicochemical properties and biological activities of compounds. The existence of difluoromethyl may affect its metabolic pathway in organisms.
    In terms of toxicity, some organic fluorinated compounds have certain toxicity. However, it is difficult to accurately determine the degree of toxicity based on the structure alone. Because the toxicity of a compound is not only related to the structure, but also closely related to the dose, exposure route and biological species.
    If ingested orally, the solubility, stability and degree of absorption of the compound in the gastrointestinal tract will affect its toxicity. If the solubility is good and it is easier to be absorbed, it may have a more significant impact on the body.
    If it is exposed to the skin, its ability to penetrate the skin is also critical. If it can easily penetrate the skin, it may enter the blood circulation, and then have effects on various tissues and organs of the body.
    In an industrial production environment, if its volatile vapor is inhaled, it will irritate or damage the respiratory system. At the same time, the potential chronic toxicity of long-term low-dose exposure cannot be ignored, such as cumulative damage to specific organs, effects on the reproductive system or immune system, etc.
    However, there is no conclusive experimental data and research conclusion to clarify the specific safety properties and toxicity of 4-difluoromethyl-2-methyl-thiazole-5-carboxylic acid in detail. To know for sure, rigorous toxicological experiments, such as acute toxicity experiments, subchronic and chronic toxicity experiments, and genetic toxicity experiments, etc., can only be obtained through the observation and detection of experimental animals. Scientific and accurate safety and toxicity assessments can be obtained.