4 5 Dimethyl 2 2 Methylpropyl 2 5 Dihydro 1 3 Thiazole
quinoline thiophene imidazole thiazole

4,5-dimethyl-2-(2-methylpropyl)-2,5-dihydro-1,3-thiazole

    Specifications

    HS Code

    465364

    Chemical Formula C10H17NS
    Molar Mass 183.314 g/mol
    Physical State Liquid (presumably, typical for many thiazole derivatives)
    Boiling Point Estimated based on similar compounds, around 200 - 250 °C
    Density Approximated around 0.9 - 1.1 g/cm³ based on related structures
    Solubility In Water Low solubility, thiazole derivatives are generally hydrophobic
    Solubility In Organic Solvents Soluble in common organic solvents like ethanol, acetone, dichloromethane
    Odor May have a characteristic sulfur - containing heterocyclic odor, often pungent
    Flammability Flammable, like most organic compounds

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    Frequently Asked Questions

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    What are the physical properties of 4,5-dimethyl-2- (2-methylpropyl) -2,5-dihydro-1,3-thiazole?
    4,5-Dimethyl-2- (2-methylpropyl) -2,5-dihydro-1,3-oxazole, which is an organic compound. Its physical properties are as follows:
    Viewed at room temperature and pressure, it is either a colorless to light yellow liquid or a crystalline solid, depending on the intermolecular force and the lattice arrangement. If the intermolecular force is strong and the lattice is regular and orderly, it tends to form a crystalline solid; if the intermolecular force is weak and the arrangement is relatively disordered, it mostly exists in the form of a liquid.
    Smell, it has a special organic odor, but this odor may vary due to concentration differences. When the concentration is low, it may have a weak and non-pungent smell; when the concentration is high, the smell may be more intense and irritating.
    When it comes to boiling point, because the molecular structure contains multiple alkyl groups such as methyl and propyl, the intermolecular force is mainly van der Waals force, resulting in the boiling point being affected by the molecular weight and structure. When the relative molecular weight increases, the intermolecular van der Waals force increases, and the boiling point also increases. The boiling point of this compound may be within a specific range, and the specific value needs to be accurately determined by experiments.
    In terms of melting point, the symmetry and compactness of the molecular structure have a great influence on its melting point. If the molecular structure is symmetrical and tightly packed in the lattice, the intermolecular force is enhanced, and the melting point will also increase. On the contrary, if the structure is asymmetric, it is difficult to closely arrange the molecules, and the melting point is relatively low.
    In terms of solubility, because it is an organic compound, according to the principle of "similar miscibility", it may have good solubility in common organic solvents such as ethanol, ether, chloroform, etc. Because organic solvents and the molecules of the compound can form similar intermolecular forces, such as van der Waals forces, to promote dissolution. In water, because water is a polar molecule, the polarity of the compound is relatively weak, and the force between the water molecules is small, so the solubility in water is poor.
    What are the chemical properties of 4,5-dimethyl-2- (2-methylpropyl) -2,5-dihydro-1,3-thiazole
    4,5-Dimethyl-2- (2-methylisopropyl) -2,5-dihydro-1,3-oxazole This compound has many chemical properties. The methyl, isopropyl and other alkyl groups contained in its structure make the compound have a certain lipid solubility. Because the alkyl group is a hydrophobic group, it has good solubility in organic solvents.
    From the structure of the oxazole ring it contains, the oxazole ring has certain aromaticity and stability. Aroma endows the compound with relatively stable chemical properties, and under some conventional conditions, it is not prone to violent reactions. However, the nitrogen and oxygen atoms on the oxazole ring have certain electronic effects, and the lone pair electrons on the nitrogen atom make the ring have certain nucleophilicity. Under appropriate conditions, it may react with electrophilic reagents.
    In addition, the dihydrogen structure in the compound makes the molecule partially unsaturated, which is more reactive than the fully saturated structure. Under specific redox conditions, the dihydrogen part may be oxidized and converted into the corresponding unsaturated structure; or under hydrogenation conditions, it may be further saturated. At the same time, there is a steric hindrance effect between the substituents in the molecule, which affects the selectivity and rate of its chemical reaction. In areas with large steric resistance, the reagents are difficult to access and the reactivity decreases; while in areas with small steric resistance, the reaction is relatively easy to occur.
    What is the synthesis method of 4,5-dimethyl-2- (2-methylpropyl) -2,5-dihydro-1,3-thiazole?
    To prepare 4% 2C5-dimethyl-2- (2-methylisopropyl) -2,5-dihydro-1,3-oxazole, the following method can be followed.
    First take an appropriate amount of starting material, when the compound with suitable substituents is used as the base. Select related compounds containing methyl and isopropyl structures, and then undergo a series of ingenious reactions to achieve this goal.
    First alkylation is performed to introduce methyl and isopropyl groups. This reaction requires careful temperature control and control, and appropriate catalysts and reaction solvents are selected. If an inert organic solvent is used as the medium, at a moderate temperature, the reactants and specific alkylating reagents are fully reacted with the help of the catalyst. The amount and activity of the catalyst are crucial, and the reaction will be slow if the amount is small, and more may cause side reactions.
    After the alkylation is completed, go to the step of constructing the oxazole ring. This is a key step, and specific cyclization reagents and conditions are often required. Or in an alkaline environment, a cyclization accelerator is used to assist the cyclization and condensation of specific functional groups in the molecule. In this process, the strength of basicity, the type and amount of cyclization accelerator have a profound impact on the reaction process and product purity. < Br >
    During the reaction, real-time monitoring is required by various analytical methods, such as thin layer chromatography (TLC), to clarify the reaction progress and product formation. If the reaction is not as expected, the reaction conditions can be adjusted in a timely manner, such as increasing or decreasing the amount of reagents, changing the temperature or reaction time.
    When the reaction is generally completed, the product still contains impurities and needs to be separated and purified. It can be initially separated by extraction method, followed by column chromatography for further purification. According to the different partition coefficients of the product and impurities in the stationary and mobile phases, efficient separation can be achieved, and a high-purity 4% 2C5-dimethyl-2 - (2-methyl isopropyl) -2,5-dihydro-1,3-oxazole can be obtained. The whole synthesis process requires fine operation and strict control of each link conditions to achieve satisfactory results.
    In which fields is 4,5-dimethyl-2- (2-methylpropyl) -2,5-dihydro-1,3-thiazole used?
    4,5-Dimethyl-2- (2-methylpropyl) -2,5-dihydro-1,3-oxazole, which has important applications in pharmaceuticals, materials science and organic synthesis.
    In the pharmaceutical field, its special molecular structure can act as a key intermediate for the synthesis of compounds with specific biological activities. For example, in the development of new antimicrobial drugs, this substance can be used as a starting material, and through a series of chemical reactions, other functional groups can be introduced to shape drug molecules that can precisely act on specific targets in bacteria, so as to achieve antibacterial effect.
    In the field of materials science, 4,5-dimethyl-2- (2-methylpropyl) -2,5-dihydro-1,3-oxazole can participate in the preparation of polymer materials. By polymerizing with other monomers, the material is endowed with unique properties. For example, the preparation of engineering plastics with good thermal stability and mechanical properties is used in the manufacture of automotive parts, electronic equipment shells, etc., to improve product durability and reliability.
    The field of organic synthesis is also its place to show its talents. As an organic synthesis block, with its structural characteristics, it can participate in the construction of various complex organic molecules. Chemists can use this compound to design clever synthesis routes according to the structural requirements of the target product, and realize multi-step reactions to obtain high-value-added organic compounds, providing an important material basis for the development of organic synthetic chemistry.
    What is the market outlook for 4,5-dimethyl-2- (2-methylpropyl) -2,5-dihydro-1,3-thiazole?
    4,5-Dimethyl-2- (2-methylpropyl) -2,5-dihydro-1,3-oxazole, this is an organic compound. Looking at its market prospects, it can be analyzed from many aspects.
    First, in the field of pharmaceutical chemistry, organic compounds are often important raw materials or intermediates for drug synthesis. If they have specific chemical structures and activities, or can participate in a variety of drug preparation processes. With the continuous advancement of pharmaceutical research and development, the demand for novel and unique organic compounds may increase day by day. If this compound is confirmed to have positive effects on the treatment of specific diseases by research, or can be used as a key intermediate in the production of related drugs, the market prospect may be extremely broad.
    Second, in the field of materials science, some organic compounds may exhibit excellent physical and chemical properties after proper treatment and modification, and can be used to make special materials. For example, in the synthesis of polymer materials, they may be used as structural units to endow materials with specific mechanical properties, thermal stability or optical properties. With the development of high-tech industries, the demand for high-performance materials continues to rise. If this compound can meet the preparation requirements of a certain type of high-performance materials, its market potential should not be underestimated.
    Third, considering the cost of research and development and the technical difficulty, if the synthesis process of the compound is complicated, the required raw materials are scarce or expensive, and large-scale production is difficult, it will restrict its marketing activities and applications. On the contrary, if the synthesis process is relatively simple, the raw materials are easy to obtain and the cost is controllable, it will be easier to achieve industrial production, and the market competitiveness will also be enhanced.
    Fourth, the market competition situation is also a key factor. If there are alternatives with similar functions and lower costs in the market, its market expansion may encounter obstacles; conversely, if its performance is unique and cannot be replaced, the market prospect is more optimistic.
    In summary, the market prospect of 4,5-dimethyl-2 - (2-methylpropyl) -2,5-dihydro-1,3-oxazole depends on the comprehensive action of multiple factors, covering the needs of medicine, materials and other application fields, synthesis costs, technical difficulties and market competition, etc. Only by comprehensive weighing can we have a more accurate judgment on its market prospect.