Ethyl 4 Methylthiazole 5 Carboxylate
quinoline thiophene imidazole thiazole

Ethyl 4-methylthiazole-5-carboxylate

    Specifications

    HS Code

    451413

    Chemical Formula C8H9NO2S
    Molar Mass 183.23 g/mol
    Appearance Typically a solid
    Color May be white to off - white
    Solubility In Water Low solubility
    Solubility In Organic Solvents Soluble in some organic solvents like ethanol, acetone
    Odor May have a characteristic odor
    Stability Stable under normal conditions if stored properly

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    General Information
    Where to Buy Ethyl 4-methylthiazole-5-carboxylate in China?
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    Frequently Asked Questions

    As a leading Ethyl 4-methylthiazole-5-carboxylate 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 main uses of Ethyl 4-methylthiazole-5-carboxylate?
    Ethyl + 4 - methylthiazole - 5 - carboxylate (ethyl 4 - methyl - 5 - thiazole carboxylate) is widely used in the field of chemical medicine.
    It is often a key intermediary in the synthesis of medicine. When many drugs are developed, based on this, other compounds can be derived, or have antibacterial and anti-inflammatory effects. Due to its unique structure, it can be combined with other reagents by organic synthesis to form a variety of pharmacoactive groups.
    In the field of fine chemistry, it is also indispensable. Or used in the creation of fragrances, with their special chemical properties, give fragrances a different flavor, increase the complexity and uniqueness of their aroma. It can also help pesticide synthesis, participate in the preparation of pesticides with insecticidal and bactericidal properties, and strengthen the prevention and control effectiveness of pesticides against pests and diseases through reasonable molecular design and reaction.
    Furthermore, in the field of scientific research and exploration, chemists borrow 4-methyl-5-thiazolecarboxylate ethyl ester to explore the mechanism and laws of organic reactions. Using it as a substrate, various reaction experiments were carried out to gain insight into the influence of reaction conditions and catalysts on product formation, and contributed to the theoretical improvement of organic synthetic chemistry.
    In conclusion, ethyl 4-methyl-5-thiazolecarboxylate plays an important role in chemical engineering, medicine, and scientific research, promoting technological progress and innovation in various fields.
    What are the synthetic methods of Ethyl 4-methylthiazole-5-carboxylate?
    Ethyl 4-methylthiazole-5-carboxylate (ethyl 4-methylthiazole-5-carboxylate) is commonly synthesized in the following ways.
    First, sulfur-containing compounds and nitrogen-containing compounds are used as starting materials and are formed by condensation reaction. For example, ethyl acetoacetate is used as the starting material and interacts with the sulfide reagent first to form a sulfur-containing structure, and then nitrogen atoms are introduced. In this process, the reaction conditions need to be carefully regulated. Temperature, pH and the ratio of reactants are all key. If the temperature is too high, it is easy to cause side reactions and the product is impure; if the temperature is too low, the reaction rate is slow and takes a long time. < Br >
    Second, prepared by cyclization reaction. Select a suitable open-chain compound, and through the action of a specific catalyst, promote the formation of intramolecular rings, and then generate the target product. This path requires the selection of efficient and selective catalysts in order to improve the reaction yield and product purity. For example, some metal catalysts can effectively catalyze the cyclization process in specific reaction systems. However, it is necessary to pay attention to the strict requirements of the reaction conditions, and the recovery and reuse of the catalyst also need to be considered.
    Third, use a substitution reaction. Using a compound with a thiazole ring as a substrate, a methyl and carboxyethyl ester group is introduced at a suitable position through a substitution reaction. This method requires attention to the selectivity of the substitution check point to avoid substitution in other unnecessary positions, which affects the structure and purity of the product.
    When synthesizing this compound, no matter what method is used, the reaction process needs to be carefully controlled, and the reaction conditions at each step should be optimized to obtain high purity Ethyl 4 - methylthiazole - 5 - carboxylate.
    What are the physical properties of Ethyl 4-methylthiazole-5-carboxylate?
    Ethyl 4-methylthiazole-5-carboxylic acid ester is one of the organic compounds. Its physical properties are quite impressive, so let me tell them one by one.
    Looking at its properties, under normal temperature and pressure, it is often in a liquid state. The color of this substance is mostly colorless to light yellow, and the color is relatively light and quite clear.
    When it comes to boiling point, it is within a certain temperature range. The specific value varies slightly due to different measurement conditions, but it is roughly within a certain range. This boiling point characteristic is crucial in its separation, purification and related chemical operations, and the operator can control the change of its state accordingly.
    In terms of melting point, there are also specific values. Knowing its melting point can guide the identification of the substance and the control of the relevant reaction process.
    Solubility is also a key property. In organic solvents, it exhibits certain solubility characteristics. For example, in common organic solvents such as ethanol and ether, it can exhibit good solubility and can be miscible with these solvents to form a uniform system. However, in water, its solubility is quite limited, only slightly soluble. The difference in solubility depends on the molecular structure and polarity of the compound itself.
    Density is also an important part of its physical properties. Its density also has a specific value, which is of important reference value for related chemical production, measurement and transportation, and is related to the accuracy and safety of operation.
    In summary, the physical properties of ethyl 4-methylthiazole-5-carboxylate are diverse, and it is of great significance in many fields such as chemical industry and scientific research. Operators must know its properties in detail before they can make good use of it.
    What are the chemical properties of Ethyl 4-methylthiazole-5-carboxylate?
    Ethyl 4-methylthiazole-5-carboxylate is an organic compound with unique chemical properties.
    It has the generality of esters because it contains ester groups (− COO −). Under the catalysis of acid or base, hydrolysis can occur. Hydrolyzed under acidic conditions, 4-methylthiazole-5-carboxylic acid and ethanol are slowly generated; hydrolyzed in alkaline environment is easier to obtain carboxylate and ethanol. This is a typical reaction of esters, just like many esters can be hydrolyzed and transformed under different conditions.
    The compound contains thiazole ring, which endows it with certain aromatic properties and stability. The presence of the thiazole ring allows the molecular conjugation system to expand, affecting its electron cloud distribution and chemical activity. Due to the difference in electronegativity of nitrogen and sulfur atoms on the thiazole ring, the electron cloud is biased towards nitrogen and sulfur, resulting in uneven electron cloud density on the ring, and the electrophilic substitution reaction is prone to occur at specific locations. For example, under appropriate conditions, halogenated reagents can attack the active check point on the ring to generate halogenated derivatives.
    Its methyl is connected to the thiazole ring, and methyl is the power supply radical. It affects the molecular electron cloud distribution through induction effects, which increases the electron cloud density of the thiazole ring, which in turn affects the electrophilic substitution reaction activity and check point selectivity.
    The chemical properties of Ethyl 4-methylthiazole-5-carboxylate are derived from the interaction of its ester group, thiazole ring and methyl group. These properties are of great significance in organic synthesis, medicinal chemistry and other fields. They can be used as synthetic intermediates to participate in various organic reactions and construct more complex compound structures.
    What is the price range of Ethyl 4-methylthiazole-5-carboxylate in the market?
    Above the city, the quality of the product depends on the supply and demand end. As for Ethyl + 4 - methylthiazole - 5 - carboxylate, its price is determined.
    In the past, the quality of the product in the "Tiangong" and the general product are different because of its price, quantity, and place of origin. Today, Ethyl + 4 - methylthiazole - 5 - carboxylate is also the same. If there is a lot of land, the supply will be in demand, and the supply will be flat; if the land is thin, the demand will be huge, and the demand will be high.
    And the use of this product or the chemical industry. If the demand for a certain field increases sharply, it will also be high. In addition, the ease of creation and the use of creation are all different. If the method of creation is easy, it will be convenient for you, and the cost can be suppressed; otherwise, the cost will rise.
    However, the city will see a lot of waves, so that you can know the cause of the pattern, and also make its cut. Or as low as 10% value, or as high as hundreds or thousands of values, it is possible to cover it in one word.