5 1 Hydroxy 1 Methylethyl 2 Propyl 3h Imidazole 5 Carboxylic Acid Ethyl Ester
quinoline thiophene imidazole thiazole

5-(1-hydroxy-1-methylethyl)-2-propyl-3h-imidazole-5-carboxylic acid ethyl ester

    Specifications

    HS Code

    739873

    Chemical Formula C11H18N2O3
    Molecular Weight 226.27
    Appearance Solid (usually)
    Physical State At Room Temperature Solid
    Melting Point Data needed
    Boiling Point Data needed
    Solubility In Water Data needed
    Solubility In Organic Solvents Data needed
    Density Data needed
    Flash Point Data needed
    Pka Data needed
    Logp Data needed

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    As a leading 5-(1-hydroxy-1-methylethyl)-2-propyl-3h-imidazole-5-carboxylic acid ethyl ester supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

    5- (1-hydroxy-1-methylethyl) What is the chemical structure of -2-propyl-3h-imidazole-5-carboxylic acid ethyl ester?
    The name of this compound is 5- (1-hydroxy-1-methethyl) - 2-propyl-3H-imidazole-5-carboxylic acid ethyl ester. In ancient words, the chemical structure of this compound is explained as follows:
    Looking at the name of this compound, "5- (1-hydroxy-1-methethyl) ", it can be seen that at the 5th position of the imidazole ring, there is a group attached. This group is composed of "1-hydroxy-1-methethyl", which is like a leaf attached to a specific position in the trunk. " 1-Hydroxy ", hydroxyl, a group connected to oxygen and hydrogen, has active chemical properties and can participate in many reactions." 1-methyl ", methyl is a group composed of carbon and hydrogen, added to ethyl to change its spatial structure and chemical properties.
    " 2-propyl ", indicating that at the 2nd position of the imidazole ring, the propyl group is connected. Propyl is an alkyl group containing three carbon atoms, which extends on the side of the imidazole ring and affects the spatial layout and hydrophobicity of the molecule as a whole.
    "3H-imidazole", the imidazole ring is the core structure of this compound, with a special conjugate system, which gives the molecule a unique electron distribution and reactivity. "3H" identifies its specific atomic number and bonding method, which is the identification of the ring structure.
    "Ethyl carboxylate", at the 5 position of the imidazole ring, in addition to the above groups, there is also a carboxylic acid ethyl ester group. Ethyl carboxylate is formed by esterification of carboxyl groups and ethanol. This group imparts certain chemical stability and reaction check points to the molecule, such as hydrolysis.
    Overall, this compound is composed of an imidazole ring as the core, with (1-hydroxy-1-methylethyl) and carboxylic acid ethyl group at the upper 5 position, and propyl group at the second position. Each group interacts to co-construct its unique chemical structure, which determines its performance in chemical reactions and biological activities.
    5- (1-hydroxy-1-methylethyl) What are the main uses of -2-propyl-3h-imidazole-5-carboxylic acid ethyl ester?
    5- (1-hydroxy-1-methethyl) - 2-propyl-3H-imidazole-5-carboxylic acid ethyl ester, which is an organic compound. It has a wide range of uses in the field of medicine and can be used as an intermediate for synthesizing drugs. When developing medicine, chemists use it as a basis and add specific functional groups through a series of chemical reactions to build complex chemical structures, aiming to create new drugs with specific pharmacological activities, such as developing therapeutic drugs targeting specific disease targets, such as some innovative drugs used to regulate human physiology or fight diseases.
    It also has potential application value in the field of materials science. Due to its special chemical structure, it may participate in material synthesis reactions, giving materials unique properties. For example, in the preparation of polymer materials, it is introduced into the polymer chain as a functional monomer, so that the material has better solubility, thermal stability or mechanical properties, and is used to manufacture new materials with excellent performance to meet different industrial needs.
    In the field of organic synthetic chemistry, it is often regarded as a key intermediate, participating in the construction of many complex organic molecules. With the help of the activity check point in its molecules, it can combine with other organic compounds through various organic reactions, such as esterification reactions, substitution reactions, etc., to expand the complexity and diversity of molecular structures, providing an important cornerstone for the synthesis of various organic compounds, and promoting the development and innovation of organic synthetic chemistry.
    What are the synthesis methods of 5- (1-hydroxy-1-methylethyl) -2-propyl-3h-imidazole-5-carboxylic acid ethyl ester?
    The method of preparing 5- (1-hydroxy-1-methylethyl) -2-propyl-3H-imidazole-5-carboxylic acid ethyl ester has been explored by many scholars in the past, and the best methods are recorded here.
    First, use a compound containing imidazole as the starting material. First, put this imidazole compound into a suitable reactor, add an appropriate amount of solvent, such as alcohol solvent, to create a homogeneous reaction environment. Then, slowly add a specific halogenated alkyl hydrocarbon, which needs to contain a propyl structure, and add an appropriate amount of base to promote the nucleophilic substitution reaction. During the reaction, it is necessary to precisely control the temperature, so that the temperature is maintained at a certain range, such as between [X] ° C and [X] ° C, and stirred continuously. After several hours, when the reaction reaches the expected level, the preliminary product is obtained. Then, the preliminary product is extracted, washed, dried and other post-processing steps to purify the product.
    Second, another compound containing a specific functional group is also used as the starting point. First, the compound undergoes a condensation reaction with a carbonyl-containing reagent. This condensation reaction needs to be carried out in the presence of a specific catalyst, and the amount of catalyst needs to be carefully considered. During the reaction process, the pH of the reaction system also needs to be strictly controlled, and a buffer solution can be used to maintain a certain pH range. After the condensation reaction is completed, a group containing 1-hydroxy-1-methylethyl is introduced. This step can be achieved by reacting with the corresponding alcohol derivatives. The reaction conditions such as temperature and reaction time need to be carefully adjusted to make the reaction proceed smoothly in the desired direction. The final product also needs to undergo a series of separation and purification operations to obtain high-purity 5- (1-hydroxy-1-methylethyl) -2-propyl-3H-imidazole-5-carboxylic acid ethyl ester.
    Furthermore, a multi-step series reaction method is also used. The basic structure of the imidazole ring is first constructed from the starting material through several steps of reaction. Each step focuses on the optimization of reaction conditions, such as the proportion of reactants, the choice of reaction solvent, and the regulation of reaction temperature and time. After the imidazole ring structure is formed, groups such as 2-propyl and 5- (1-hydroxy-1-methethyl) are introduced in sequence, and after each group is introduced, the products are properly purified to reduce the interference of side reaction products. So many steps are carefully operated, and the final product is obtained. These methods have their own advantages and disadvantages, and they need to be carefully selected according to actual needs and conditions.
    5- (1-hydroxy-1-methylethyl) What are the physical properties of -2-propyl-3h-imidazole-5-carboxylic acid ethyl ester?
    5- (1-hydroxy-1-methethyl) - 2-propyl-3H-imidazole-5-carboxylic acid ethyl ester, the physical properties of this substance are very important, related to its application in various fields.
    Its appearance is mostly white to white-like crystalline powder, like fine snow, pure and delicate, and it is very pleasing to the eye. This form is easy to store and use, and it is easy to handle in various preparation processes.
    In terms of melting point, it is in a specific temperature range, which is the key node of its transition from solid to liquid. Accurate determination of the melting point is of great significance for determining the purity of the substance. If the melting point is accurate and the melting range is narrow, it indicates that the purity of the substance is quite high; conversely, if the melting range is wide, it may contain impurities.
    Solubility is also a key property. It exhibits good solubility in organic solvents such as ethanol and acetone, and can disperse rapidly like a salt in water to form a uniform solution. This property makes it easier to mix and react with other substances when preparing a solution dosage form or performing a chemical reaction. In water, its solubility is relatively limited, just like oil floating in water, with only a small amount of dissolution, which also determines that its application in aqueous systems requires special consideration.
    In addition, the density of the substance also has its own unique value, although invisible but existing, which has an important impact on the calculation of its dosage in the preparation and the proportion control when mixed with other substances. Only by knowing its density can it be accurately prepared to ensure the quality and performance of the product are stable.
    The above physical properties are the cornerstones of in-depth understanding and rational use of 5- (1-hydroxy-1-methylethyl) -2-propyl-3H-imidazole-5-carboxylic acid ethyl ester. It has far-reaching significance in the research and production practice of chemical industry, medicine and other fields.
    5- (1-hydroxy-1-methylethyl) What is the market outlook for -2-propyl-3h-imidazole-5-carboxylic acid ethyl ester?
    5- (1-hydroxy-1-methylethyl) -2-propyl-3H-imidazole-5-carboxylic acid ethyl ester, the market prospect of this product is related to many parties, and listen to me in detail.
    From the perspective of the field of self-made drugs, this compound may have unique medicinal potential. Today's pharmaceutical research is increasingly advanced, and there is a great demand for compounds with specific structures and activities. If this ester compound can exhibit unique biological activities, such as anti-inflammatory, anti-tumor or physiological functions, it will surely attract the attention of pharmaceutical companies. In order to expand their product lines and enhance their competitiveness, pharmaceutical companies will definitely invest in the research and development of related drugs. At that time, its market demand may be like bamboo shoots, rising steadily.
    In the chemical industry, this compound can be used as an important intermediate. The chemical synthesis process is complex and diverse, and intermediates are the key to connecting each reaction step. If it is indispensable in the synthesis of specific high-value-added products, and the preparation process is feasible and the cost is controllable, chemical companies must compete. The scale of chemical production is huge. Once its position in the synthesis route is determined, its dosage will be measured in a considerable amount, and the market prospect is bright.
    However, there are also challenges. The research and development of new drugs takes a long time, the investment is huge, and the clinical trial is full of risks. If the pharmaceutical research of this compound does not meet expectations, the market road may be bumpy. In the chemical industry, if the preparation process is complicated, expensive, or environmentally friendly, it will also limit its large-scale application.
    Overall, if 5- (1-hydroxy-1-methylethyl) -2-propyl-3H-imidazole-5-carboxylic acid ethyl ester can overcome the research and development and production problems, it is expected to occupy a place in the pharmaceutical and chemical markets, with broad prospects; otherwise, it may be trapped in the development bottleneck and the prospect is uncertain.