4 Methyl 1 3 Thiazole 5 Carbaldehyde
quinoline thiophene imidazole thiazole

4-Methyl-1,3-thiazole-5-carbaldehyde

    Specifications

    HS Code

    790292

    Name 4-Methyl-1,3-thiazole-5-carbaldehyde
    Chemical Formula C5H5NOS
    Molar Mass 127.164 g/mol
    Appearance Solid or liquid (depending on conditions)
    Solubility In Water Low (organic compound with non - polar parts)
    Solubility In Organic Solvents Soluble in common organic solvents like ethanol, acetone
    Odor Characteristic odor (specific data needed)

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    General Information
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    Frequently Asked Questions

    As a leading 4-Methyl-1,3-thiazole-5-carbaldehyde supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

    4-Methyl-1, what is the chemical property of 3-thiazole-5-carbaldehyde
    4-Methyl-1,3-thiazole-5-formaldehyde is an organic compound. It has unique chemical properties and is very important in the field of organic synthesis.
    Looking at its chemical structure, the thiazole ring system is stable, and the methyl group and aldehyde group on the ring endow the compound with special reactivity. The aldehyde group has high reactivity and can participate in many important organic reactions. For example, it can occur typical oxidation reaction of aldehyde. Under the action of suitable oxidants, the aldehyde group can be converted into carboxyl group to generate 4-methyl-1,3-thiazole-5-carboxylic acid. This reaction is often used in organic synthesis to construct complex compounds containing carboxyl groups.
    Furthermore, the aldehyde group can undergo a reduction reaction, and can be converted into a hydroxyl group with a suitable reducing agent to obtain 4-methyl-1,3-thiazole-5-methanol. This alcohol compound can participate in many reactions such as etherification and esterification as an intermediate in subsequent reactions.
    The aldehyde group can also participate in nucleophilic addition reactions. For example, acetal reacts with alcohols, and under acid catalysis, an acetal structure is formed. This acetal structure is often used as a protective group in organic synthesis to protect the aldehyde group from participating in some specific reaction steps. After the reaction is completed, it can be deprotected under specific conditions to restore the aldehyde group.
    The methyl group on the thiazole ring also has a certain influence. Methyl group is the power supply group, which can increase the electron cloud density of the thiazole ring, which in turn affects the reactivity at other positions on the ring. For example, in the electrophilic substitution reaction, the power supply effect of methyl group will make the reaction more likely to occur at a specific position of the thiazole ring, which affects the reaction selectivity.
    In addition, the compound contains heteroatoms such as nitrogen and sulfur, which also attracts attention in some biological activity studies, or has potential biological activity, and can be used in pharmaceutical chemistry and other fields.
    4-Methyl-1, what are the main uses of 3-thiazole-5-carbaldehyde
    4-Methyl-1,3-thiazole-5-carbalaldehyde (4-methyl-1,3-thiazole-5-formaldehyde) is a key substance in the field of organic compounds and has important uses in many fields.
    First, in the field of pharmaceutical chemistry, as a key intermediate, it plays an important role in the synthesis of many drugs. Because of its unique chemical structure, it can participate in various chemical reactions and help build complex drug molecular structures. By chemically modifying and modifying it, compounds with specific pharmacological activities can be created to develop new drugs for the treatment of various diseases, such as antibacterial, anti-inflammatory, anti-tumor and other drugs.
    Second, in the field of materials science, this compound may be used to synthesize special functional materials. For example, by virtue of its reaction properties with other substances, it can prepare materials with special optical, electrical or mechanical properties, or be applied to cutting-edge fields such as optoelectronic materials and sensor materials, providing new opportunities for the innovation and development of materials science.
    Third, in the field of fragrance industry, 4-Methyl-1,3-thiazole-5-carbalaldehyde can act as a fragrance component because of its unique smell. It can add a unique flavor to the formulation of flavors and fragrances, and is widely used in food, cosmetics, detergents and other industries to enhance the aroma quality and attractiveness of products.
    Fourth, in the field of organic synthetic chemistry, it is an extremely useful synthetic building block. Chemists can use its active functional groups to construct more complex organic molecules through a series of organic reactions, such as nucleophilic addition and condensation reactions, to expand the boundaries of organic synthesis and lay the foundation for basic research and application development of organic chemistry.
    What is the synthesis method of 4-Methyl-1, 3-thiazole-5-carbaldehyde?
    The synthesis of 4-methyl-1,3-thiazole-5-formaldehyde is an important topic in the field of organic synthesis. There are several common methods for synthesizing this compound.
    First, it can be started from the thiazole ring containing a suitable substituent. Appropriate raw materials are selected, and through a series of reactions, the thiazole ring is constructed and methyl and aldehyde groups are introduced. For example, based on a compound containing sulfur and nitrogen, the methyl group is introduced into a specific position through nucleophilic substitution reaction, and then the aldehyde group is introduced into the 5-position of the thiazole ring through oxidation or other suitable reactions. In this process, the reaction conditions such as temperature, solvent and catalyst dosage need to be carefully regulated. Too high or too low temperature can affect the rate and selectivity of the reaction. Suitable solvents can promote the dissolution of the reactants and improve the reaction efficiency. The choice and dosage of catalysts are also crucial to accelerate the reaction process and ensure that the reaction proceeds according to the expected path.
    Second, the strategy of gradually constructing a thiazole ring can also be used. First, the intermediate containing part of the thiazole ring structure is prepared, and then the ring is formed by condensation and cyclization. During the cyclization process, the reaction conditions are precisely controlled so that methyl and aldehyde groups are formed at the target location. For example, using specific sulfur-containing reagents and nitrogen-containing reagents, condensation is formed under specific conditions to form a thiazole ring skeleton, and then the required methyl and aldehyde groups are introduced at the predetermined location through functional group transformation. This method requires a deep understanding of the mechanism of each step of the reaction in order to accurately control the reaction process and avoid side reactions.
    Synthesis of 4-methyl-1,3-thiazole-5-formaldehyde requires careful selection of appropriate synthesis routes according to actual conditions, and strict control of the conditions of each reaction step, so that the target product can be obtained efficiently and with high purity.
    What is the market price of 4-Methyl-1, 3-thiazole-5-carbaldehyde
    I see what you are asking about the market price of 4-Methyl-1,3-thiazole-5-carbalaldehyde. However, the price of this product is difficult to determine. The price of the cover often changes for a variety of reasons.
    First, the price of the raw material is the main factor. If the price of the various raw materials required to make this product fluctuates, the price of 4-Methyl-1,3-thiazole-5-carbalaldehyde will also move accordingly. If the raw material is scarce, and there are many people who want it, the price will be high; if the raw material is abundant and the supply exceeds the demand, the price may drop.
    Second, the method of preparation is also related to the price. The subtle and simple method can reduce the cost, price or people; if the preparation method is cumbersome and complicated, and requires more effort and more money, the price will be high.
    Furthermore, the supply and demand of the market has a huge impact on the price. If there are many people in need of this product in the market, but there are few suppliers, the price will increase; conversely, if the supply exceeds the demand, the merchant will sell its goods or reduce the price.
    In addition, the production area, the reputation of the manufacturer, etc., can also make the price different. Made by famous factories, or because of high quality, the price is higher than that of other factories; different regions, due to different taxes, transportation and other fees, the price is also different.
    Therefore, to know the exact market price of 4 - Methyl - 1,3 - thiazole - 5 - carbalaldehyde, we should carefully investigate the raw material price, preparation method, supply and demand status and other relevant reasons, or consult the industry merchants and experts to obtain a more accurate number.
    4-Methyl-1, 3-thiazole-5-carbaldehyde What are the precautions in storage and transportation?
    4-Methyl-1,3-thiazole-5-formaldehyde is an organic compound. When storing and transporting, the following matters should be paid attention to:
    First, storage. This compound should be placed in a cool, dry and well-ventilated place. Because a cool environment can slow down its chemical reaction rate and reduce the risk of deterioration; dry conditions can avoid adverse reactions such as hydrolysis caused by the presence of moisture; good ventilation can prevent the accumulation of harmful gases. Do not store in high temperature or humid places. High temperature can easily cause it to evaporate, decompose, humid environment or make it react with water, thus affecting the quality. It needs to be sealed and stored to prevent contact with oxygen, carbon dioxide and other components in the air. Oxygen or cause it to oxidize, carbon dioxide may participate in some chemical reactions. At the same time, keep away from fire and heat sources, because it may be flammable, and there is a risk of combustion and explosion in case of open flames and hot topics. In addition, it should be stored separately from oxidants, acids, alkalis, etc. Because of its active chemical properties, violent reactions may occur in contact with these substances.
    Second, transportation. Before transportation, make sure that the packaging is complete and tightly sealed. Packaging materials need to have good sealing and corrosion resistance to prevent leakage. During transportation, ensure that the container does not leak, collapse, fall, etc. Transportation vehicles should also be equipped with the corresponding variety and quantity of fire equipment and leakage emergency treatment equipment to deal with emergencies. In the event of a leak, personnel from the contaminated area of the leak should be quickly evacuated to a safe area and quarantined to strictly limit access. Emergency responders need to wear self-contained positive pressure breathing apparatus and anti-toxic clothing, and do not let the leakage come into contact with combustible substances. In the case of a small leak, it can be absorbed by inert materials such as sand and vermiculite; in the case of a large leak, it is necessary to build a dike or dig a pit for containment, and cover it with foam to reduce volatilization, and then transfer it to a tanker or a special collector for recycling or transportation to a waste treatment site for disposal.