2 4 Dimethyl 1 3 Thiazole 5 Carboxylic Acid
quinoline thiophene imidazole thiazole

2,4-Dimethyl-1,3-thiazole-5-carboxylic acid

    Specifications

    HS Code

    530791

    Chemical Formula C6H7NO2S
    Molecular Weight 157.19
    Appearance Solid (usually white to off - white powder)
    Odor Typically has a characteristic thiazole - like odor
    Melting Point Specific value would need to be determined experimentally, likely in a certain temperature range
    Boiling Point Difficult to define precisely without experimental data, but would decompose before boiling in normal conditions
    Solubility In Water Low solubility in water
    Solubility In Organic Solvents Soluble in some organic solvents like dichloromethane, chloroform
    Acidity Weakly acidic due to the carboxylic acid group
    Stability Stable under normal storage conditions away from strong oxidizing agents

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    General Information
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    Frequently Asked Questions

    As a leading 2,4-Dimethyl-1,3-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 are the chemical properties of 2,4-dimethyl-1,3-thiazole-5-carboxylic acid?
    2% 2C4-dimethyl-1% 2C3-dioxolane-5-carboxylic acid is one of the organic compounds. Its chemical properties are unique and have many important characteristics.
    In this compound, due to the specific atomic connection and structural layout, it exhibits significant physical and chemical properties. In terms of chemical activity, its carboxyl group part is quite reactive. The carboxyl group is an active functional group and can participate in many chemical reactions. For example, it can neutralize with bases to form corresponding carboxylic salts and water. The principle of this reaction is that the carboxyl group can ionize hydrogen ions, and the neutralization with bases prompts the reaction to occur.
    Furthermore, its ring structure also affects the overall chemical properties. The structure of 1% 2C3-dioxane ring imparts certain stability to the molecule, but at the same time, due to factors such as the tension of the ring, atoms at specific positions are more likely to participate in the reaction. Such as the carbon atoms on the ring, under suitable conditions, the substitution reaction can be carried out. Nucleophiles can attack carbon atoms with partial positive electricity on the ring, resulting in substitution and generation of new derivatives.
    In addition, the substituent of 2% 2C4-dimethyl also changes the properties of the compound. Methyl is a power supply group, which can affect the electron cloud distribution of the molecule through induction effects. This increases the density of the atomic electron cloud connected to it, which in turn affects the polarity and reactivity of the molecule. Overall, 2% 2C4-dimethyl-1% 2C3-dioxyamyl-5-carboxylic acid exhibits various chemical properties due to the interaction of various parts, and has important application value in organic synthesis and related fields.
    What are the main uses of 2,4-dimethyl-1,3-thiazole-5-carboxylic acid?
    2% 2C4-dimethyl-1% 2C3-pentadiene-5-alkynic acid, this is an organic compound. It has a wide range of uses and plays a pivotal role in the field of organic synthesis.
    First, it is often used as a key building block when building complex organic molecular structures. Because of its unique carbon-carbon double bond and triple bond structure, it can be cleverly connected with other compounds by a variety of chemical reactions, such as addition, cyclization, etc., to build a specific carbon skeleton, laying the foundation for the synthesis of organic compounds with specific physiological activities or functions.
    Second, in the field of materials science, it can act as a monomer and polymerize to form polymer materials with special properties. For example, the formed polymer may have good optical and electrical properties, which is expected to be used in fields such as optoelectronic materials.
    Third, in the field of medicinal chemistry, because many drug molecules contain similar unsaturated bond structures, this compound can be used as an important intermediate for the synthesis of certain drugs. By modifying and modifying its structure, compounds with potential medicinal value may be obtained, providing key starting materials for the development of new drugs.
    Fourth, in the total synthesis of natural products, if the target natural product contains the corresponding structural fragments, 2% 2C4-dimethyl-1% 2C3-pentadiene-5-alkynic acid can be used as the starting material, and the structure consistent with the natural product can be constructed by gradual reaction, which can help the total synthesis of natural products, and then further explore the biological activity and mechanism of action of natural products.
    What are the synthesis methods of 2,4-dimethyl-1,3-thiazole-5-carboxylic acid?
    To prepare 2,4-dimethyl-1,3-pentadiene-5-carboxylic acid, there are many methods, and the following are common ones.
    One is to use suitable halogenated hydrocarbons and alkenolates as starting materials. Halogenated hydrocarbons need appropriate substituents, and alkenolates are carefully prepared. The two are combined in a suitable solvent, catalyzed by a base, according to the nucleophilic substitution reaction mechanism, and subsequent functional group conversion and structural adjustment to obtain the target product. In this process, factors such as the selection of halogenated hydrocarbons, the type and amount of bases, reaction temperature and time all have a great impact on the reaction process and yield.
    Second, the bonding reaction of carbon-carbon double bonds is used. Compounds containing suitable double bonds are selected to construct a carbon skeleton through synergistic reactions such as Diels-Alder reaction. This reaction requires the selection of suitable dienes and dienophiles, and the reaction conditions are strictly controlled to achieve the expected cyclization and introduction of functional groups. After hydrolysis and oxidation, the intermediate product can be converted into 2,4-dimethyl-1,3-pentadiene-5-carboxylic acid. The stereochemistry and regioselectivity of the reaction must be carefully considered to ensure the purity and yield of the product.
    Third, the conversion of carboxylic acid derivatives is aided. Starting with readily available carboxylic acid derivatives, such as esters, amides, etc., a specific substitution or addition reaction is carried out to introduce the desired methyl group and double bond structure, and then the derivative is converted into the target carboxylic acid through hydrolysis or other appropriate reactions. In this route, the activity of the derivative, the selectivity of the reagent, and the mildness of the reaction conditions are all key elements, which are related to the feasibility and efficiency of the entire synthetic path.
    What is the market outlook for 2,4-dimethyl-1,3-thiazole-5-carboxylic acid?
    Today, there are 2,4-dimethyl-1,3-dioxyamyl-5-carboxylic acids, and their market prospects are related to many aspects.
    Looking at this compound, it has a wide range of uses in the field of organic synthesis. Its unique structure can be used as a key intermediate for the preparation of a variety of complex organic compounds. For example, in pharmaceutical synthesis, it can construct a molecular structure with biological activity through a specific reaction path, or lay the foundation for the development of new drugs. Therefore, in the pharmaceutical industry, with the continuous exploration of innovative drugs, its demand may rise.
    Furthermore, in the field of materials science, it may be used to participate in the preparation of special materials. Chemical modification and polymerization may endow materials with special properties, such as excellent solubility and stability. With the rapid development of materials science, the demand for materials with unique properties is increasing, and this compound may find more application opportunities in this field.
    However, its market prospects are also influenced by multiple factors. Production costs are a key end. If the production process is complicated and the raw materials are scarce and expensive, the cost will be high, limiting its large-scale application and market expansion. Regulatory policies also have an impact. Pharmaceutical and material applications need to meet strict regulatory standards, and compliance costs may affect market competitiveness. In addition, the market competition situation should not be underestimated. If similar alternative products emerge, and the cost is low and the performance is excellent, its market share may be affected.
    Overall, 2,4-dimethyl-1,3-dioxane-5-carboxylic acids hold potential opportunities in organic synthesis, medicine, and materials, but they also need to address challenges such as cost, regulation, and competition. The future remains to be shaped by market and technological development.
    What are the precautions in the preparation of 2,4-dimethyl-1,3-thiazole-5-carboxylic acid?
    If you want to make 2,4-dimethyl-1,3-pentadiene-5-carboxylic acid, there are many things to pay attention to.
    First, the choice of raw materials is crucial. The raw materials used must be pure and of good quality. If the raw materials contain impurities, the reaction path may be shifted and the product may not be pure. Therefore, before taking the raw materials, it is necessary to check their purity and perform necessary purification to ensure that the raw materials are flawless.
    Second, the control of the reaction conditions should not be underestimated. Factors such as temperature, pressure and catalyst have a profound impact on the reaction process and product yield. If the temperature is too high, side reactions may occur; if the temperature is too low, the reaction will be slow or even stagnant. The same is true for pressure control. Improper pressure may make the reaction difficult to achieve expectations. The amount and activity of the catalyst also need to be accurately grasped, and an appropriate amount of catalyst with good activity can effectively accelerate the reaction.
    In addition, the installation and airtightness of the reaction device are also very critical. If there is an omission in the device, air or other impurities may invade, or interact with the reactants to interfere with the reaction. Therefore, after installing the device, an airtightness test must be carried out to ensure that the device is tight and there is no risk of leakage.
    Monitoring of the reaction process is also essential. Through analytical means such as chromatography and spectroscopy, real-time insight into the reaction process can be used to adjust the reaction conditions in a timely manner so that the reaction can proceed in the expected direction. If the reaction deviates from the normal track, it can also be corrected in time to avoid the product not meeting expectations.
    The separation and purification of the product after the reaction should not be ignored. After the reaction, the product is often mixed with impurities such as unreacted raw materials, by-products and catalysts. According to the physical and chemical properties of the product and impurities, an appropriate separation and purification method, such as distillation, extraction, recrystallization, etc., must be selected to obtain a high-purity product.
    In short, the preparation of 2,4-dimethyl-1,3-pentadiene-5-carboxylic acid, from the raw material to the product, all links are closely interlocked, and the negligence of any link can affect the quality and yield of the product, so everything needs to be treated with caution.