2 Dimethylaminomethyl 4 Thiazolemethanol
quinoline thiophene imidazole thiazole

2-(Dimethylaminomethyl)-4-thiazolemethanol

    Specifications

    HS Code

    286686

    Chemical Formula C6H12N2OS
    Molecular Weight 160.24 g/mol
    Appearance Typically a solid (appearance may vary based on purity and conditions)
    Physical State At Room Temperature Solid
    Odor May have a characteristic, likely organic odor
    Solubility In Water Limited solubility (amphiphilic nature may affect solubility)
    Solubility In Organic Solvents Soluble in common organic solvents like ethanol, methanol, dichloromethane
    Melting Point Data may vary, but in the range where organic solids with similar structures melt
    Stability Stable under normal conditions, but may react with strong oxidizing agents
    Pka Value Values related to its basic dimethylamino group and potentially acidic groups if applicable

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    Frequently Asked Questions

    As a leading 2-(Dimethylaminomethyl)-4-thiazolemethanol 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 main use of 2- (Dimethylaminomethyl) -4-thiazolemethanol?
    2-%28Dimethylaminomethyl%29-4-thiazolemethanol is 2- (dimethylaminomethyl) -4 -thiazolomethyl alcohol, which has a wide range of uses. In the field of medicine, it is an important pharmaceutical intermediate, and many drug synthesis depends on its participation. Due to its unique structure, it can be modified and transformed by chemical means, so it can be used to create compounds with specific pharmacological activities. For example, in the synthesis of some antibacterial drugs, 2- (dimethylaminomethyl) -4 -thiazolomethyl alcohol acts as a key starting material. After a series of reactions, it can be used to produce drugs with good inhibitory effect on specific bacteria.
    In the field of organic synthesis, it is also an extremely useful synthetic block. Because the functional groups in the molecule can participate in a variety of chemical reactions, such as nucleophilic substitution, redox, etc. Chemists can use this to build more complex organic molecular structures, providing assistance for the development of new materials and the total synthesis of natural products. For example, when synthesizing some organic materials with special optical or electrical properties, 2 - (dimethylaminomethyl) -4 -thiazolomethanol can be introduced as a structural unit to give the material unique properties.
    In addition, in the field of pesticides, it may also have potential applications. Or through appropriate derivatization, new pesticides can be developed, which can play a positive role in pest control, crop protection, etc. In conclusion, 2 - (dimethylaminomethyl) - 4 - thiazolomethyl alcohol plays an important role in many fields such as medicine, organic synthesis and pesticides due to its unique structure and reactivity.
    What are the chemical properties of 2- (Dimethylaminomethyl) -4-thiazolemethanol
    2-%28Dimethylaminomethyl%29-4-thiazolemethanol, organic compounds are also. It has unique chemical properties.
    This substance contains a specific atomic group, in which dimethylaminomethyl is connected to the thiazole ring, and is connected to the 4 position of the thiazole ring with hydroxymethyl. In terms of physical properties, it is often a solid and has a certain melting point, which is determined by intermolecular forces and crystal structures. Its solubility may vary depending on the properties of the solvent. In polar solvents, the molecule contains polar groups, such as hydroxyl and amino groups, or has a certain solubility, while in non-polar solvents The solubility may be low.
    Chemically, hydroxyl groups can participate in many reactions. The esterification reaction can occur. Under the action of the catalyst with the acid, the hydrogen of the hydroxyl group and the carboxyl group of the acid remove a molecule of water to form an ester compound. This reaction can be used to prepare derivatives with specific functions. At the same time, the amino group has a certain alkalinity, which can undergo acid-base neutralization with the acid to form corresponding salts. This property can be used to adjust its existence form and solubility in solution. The thiazole ring also endows the substance with certain stability and special reactivity. It can participate in some unique reactions of heterocyclic compounds, such as nucleophilic substitution reactions. Due to the characteristics of the electron cloud distribution on the ring, it can attract nucleophilic reagents to attack, thereby introducing new functional groups and providing a way for the synthesis of more complex compounds. In addition, the interaction between groups in the molecule, such as the effect of amino groups on the electron cloud density of the thiazole ring, affects its reactivity and selectivity. All these properties make 2-%28Dimethylaminomethyl%29-4-thiazolemethanol of great value in organic synthesis and related fields.
    What is the production method of 2- (Dimethylaminomethyl) -4-thiazolemethanol
    To prepare 2 - (dimethylaminomethyl) -4 -thiazolomethyl alcohol, the following method is often used.
    First take a suitable starting material, one of which usually contains thiazole ring structure, and has a modifiable group at a specific position, and the other raw material contains dimethylaminomethyl related structural fragments. Use the common organic synthesis path, or use the method of condensation reaction. In the reaction system, add an appropriate amount of catalyst to promote the reaction. The choice of this catalyst depends on the reaction rate and yield, and should be carefully selected according to the characteristics of the raw material and the reaction mechanism.
    When reacting, it is necessary to control the temperature, reaction time and other conditions in detail. If the temperature is too high or the side reactions increase, the yield will decrease; if the temperature is too low, the reaction rate will be slow and take a long time. The reaction time must also be precisely controlled. If it is too short, the raw materials will not be fully converted. If it is too long, the product will decompose or form other by-products.
    After the reaction is completed, the product is often mixed with impurities and must be separated and purified. Extraction can be used first to take advantage of the difference in solubility between the product and the impurities in different solvents. Then, or column chromatography can be used to further purify the product and the impurities according to the difference in the distribution coefficient between the stationary phase and the mobile phase, and obtain a pure 2 - (dimethylaminomethyl) -4 -thiazolomethanol. This method of synthesis requires the experimenter to carefully operate and control the conditions of each link in order to obtain the desired result.
    2- (Dimethylaminomethyl) -4-thiazolemethanol What are the precautions in storage and transportation
    2-%28Dimethylaminomethyl%29-4-thiazolemethanol is 2- (dimethylaminomethyl) -4 -thiazolomethyl alcohol. There are many things to pay attention to when storing and transporting this substance.
    When storing, the first environment is dry. Because of its certain hygroscopicity, if the environment is humid, it is easy to cause moisture and deterioration, which affects the quality. It should be placed in a dry and ventilated warehouse, away from water sources and moisture sources.
    Temperature is also the key. It should be controlled in a suitable range to avoid high temperature. Under high temperature, the substance may undergo chemical reactions such as decomposition and polymerization, changing its chemical structure and properties. Generally speaking, it is appropriate to store at room temperature or in a cool place, and the temperature usually does not exceed 30 ° C.
    Furthermore, keep away from fire sources and oxidants. This substance may be flammable, and it is easy to cause combustion danger in case of open flames and hot topics; and it comes into contact with oxidants, or reacts violently, and even explodes. Therefore, when storing, it should be placed separately from fire sources and oxidants, and the warehouse should be equipped with fire extinguisher materials.
    When transporting, the packaging must be firm. Use suitable packaging materials to ensure that the packaging is not damaged or leaked during handling, loading and unloading. If it is in liquid form, the packaging container should be well sealed to prevent leakage.
    Transportation vehicles should also be selected appropriately. Keep away from heat sources, fire sources, and avoid direct sunlight. During transportation, drivers and escorts should pay close attention to the condition of the goods to ensure transportation safety. When loading and unloading, the operation should be gentle, and it is strictly forbidden to drop or press to prevent material leakage due to packaging damage.
    In this way, the safety and quality of 2- (dimethylaminomethyl) -4 -thiazolomethanol during storage and transportation are guaranteed.
    What is the market outlook for 2- (Dimethylaminomethyl) -4-thiazolemethanol?
    2-%28Dimethylaminomethyl%29-4-thiazolemethanol is 2- (dimethylaminomethyl) -4 -thiazolomethyl alcohol, the market prospect of this substance, let me come one by one.
    Today's pharmaceutical and chemical field is developing rapidly, and new products are emerging. 2- (dimethylaminomethyl) -4 -thiazolomethyl alcohol has a wide range of uses in pharmaceutical synthesis. In recent years, the research and development of antibacterial and antiviral drugs has flourished. As a key intermediate, this compound is indispensable in the preparation of specific drugs. Due to its unique chemical structure, it can participate in many types of reactions and assist in the construction of complex active molecules.
    Looking at the market demand, with the growth of the global population and the improvement of medical level, the demand for new drugs is on the rise. This compound is not only an important raw material for drug synthesis, but also the demand is increasing. However, its production process also has challenges. The synthesis steps are complicated and the purity requirements are high, resulting in high production costs. Some manufacturers are limited by technology, and it is difficult to break through the output.
    At the scientific research level, many scientific research teams are gradually deepening their derivatization research, hoping to develop more drugs with high activity and low toxicity and side effects. This also indicates that there may be broad room for expansion in the future market. If the production technology is broken through and the cost is reduced, its market share is expected to increase significantly, and the application field may also be expanded to other fields such as pesticides and materials.
    In summary, although 2- (dimethylaminomethyl) -4 -thiazolomethyl alcohol is currently facing production difficulties, the prospects are still quite promising based on the needs of pharmaceutical and other industries, coupled with scientific research assistance. Over time, it may occupy an important position in the chemical market.