As a leading 2-oxo-2,3-dihydro-1H-imidazole-4-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 is the chemical structure of 2-oxo-2, 3-dihydro-1H-imidazole-4-carboxylate?
This 2 - oxo - 2,3 - dihydro - 1H - imidazole - 4 - carboxylate, the way of transformation, is wonderful. I will use the ancient elegance to help you solve the secret of its transformation.
In this compound, imidazole is the base of five-element nitrogen-containing atoms, with nitrogen atoms. Its framework is solid and special. The 1H above, the surface atom is on the first nitrogen position of imidazole. For 2-oxo, there is a carbonyl group (C = O) in the 2-position of XO, and this carbonyl group gives the compound a special chemical property, which can be reversed like XL, such as the addition of XL nuclei. For 2, 3-dihydro, it is clearly indicated that the 2 and 3 positions of XL have been summed, and replaced by XL, and each has one atom, so that the degree of harmony is XL.
To 4-carboxylate, there is a carboxylate (-COO -) in the 4-position of imidazole. The properties of this carboxylate also affect the integrity of the compound, such as acidity and solubility. It can be combined with gold or esterified, all because of its properties.
In this way, 2-oxo-2,3-dihydro-1H-imidazole-4-carboxylate is formed from imidazole group, plus carbonyl, carboxylate and carboxylic acid groups at 2,3 and 4 positions. Each part interacts to achieve its unique chemical properties, which can be explored in the chemical field.
What are the main uses of 2-oxo-2, 3-dihydro-1H-imidazole-4-carboxylate?
2-Oxo-2,3-dihydro-1H-imidazole-4-carboxylate has a wide range of uses. In the field of medicine, it can be used as a key intermediate for the preparation of drugs with specific biological activities. Because the imidazole ring structure plays a key role in the interaction between drugs and targets in many drug molecules, by modifying this carboxylate structure, innovative drugs with antibacterial, antiviral, antitumor and other effects can be developed.
In the field of materials science, it can be used to prepare functional materials. For example, by reacting with other organic or inorganic compounds, polymer materials with special properties can be synthesized, which may have excellent adsorption and ion exchange properties, and show potential application value in separation membranes, ion exchange resins, etc.
In chemical production, 2-oxo-2,3-dihydro-1H-imidazole-4-carboxylate is also often used as a catalyst or ligand. Its unique electronic structure and spatial configuration can effectively catalyze certain organic reactions, improve reaction efficiency and selectivity, and help chemical production to be more efficient and green.
In addition, in biochemical research, it can be used as a biochemical reagent to explore the structure and function of biological macromolecules such as proteins and nucleic acids. Because its structure is similar to the active substances in some organisms, it can provide a powerful tool for revealing the mysteries of life processes by interacting with biological macromolecules.
What are the physical properties of 2-oxo-2, 3-dihydro-1H-imidazole-4-carboxylate?
2 - oxo - 2,3 - dihydro - 1H - imidazole - 4 - carboxylate, this is an organic compound with unique physical properties. Its properties may be crystalline powder, white in color, fine and uniform in appearance, and under the microscope, the crystal structure is regular and orderly.
Regarding solubility, this substance has moderate solubility in water, and may increase significantly when the temperature increases. In polar organic solvents such as methanol and ethanol, it also exhibits good solubility, which is due to the interaction between polar groups and solvent molecules in its molecular structure. The melting point of
is an important physical constant. The melting point of the compound is in a specific temperature range. When measuring the melting point, it can be accurately measured with the help of a melting point meter. During the heating process, the compound gradually changes from a solid state to a liquid state, and the melting point range can reflect its purity. The higher the purity, the narrower the melting point range.
In terms of boiling point, due to the relatively stable structure of the compound, the boiling point is higher. When the external pressure changes, the boiling point will also change accordingly, following the law described by the Clausius-Klapelon equation.
Density is also one of its physical properties, which can be accurately determined by specific experimental methods. The density is related to the degree of compaction between molecules. The molecules of this compound are arranged or relatively tightly, so that its density is in a certain numerical range.
In addition, the compound may have certain hygroscopicity. In humid environments, it can absorb moisture in the air, causing its own weight to increase, and its appearance may change slightly, such as agglomeration. This hygroscopicity needs to be paid attention to during storage and use, and should be stored in a dry environment to maintain its stability and quality.
What is the preparation method of 2-oxo-2, 3-dihydro-1H-imidazole-4-carboxylate?
To prepare 2-oxo-2,3-dihydro-1H-imidazole-4-carboxylate, the following ancient method can be used.
First take the appropriate starting material, such as the compound containing the imidazole ring structure, and this compound needs to have a modifiable group in the appropriate position to lay the foundation for the subsequent reaction.
One method, by a specific chemical reaction, the imidazole ring can be introduced into the appropriate substituent at the 2,3 position, and the carbonyl group can be formed at the 2 position. This may be achieved by carefully selected organic reagents under mild and controlled reaction conditions. For example, a suitable acylating agent is selected, and under the action of a suitable catalyst, a specific position of the imidazole ring is acylated to introduce a carbonyl group.
Furthermore, for the formation of the 4-position carboxyl group, a specific carboxylation reaction can be used. Find a suitable carboxyl-containing reagent to interact with the imidazole ring system. Or in an alkaline environment, make the carboxyl-containing source reagent and the imidazole ring undergo nucleophilic substitution or addition-elimination reactions to successfully connect the carboxyl group at the 4-position. During the
reaction process, many factors such as temperature, reaction time, and the proportion of reactants need to be carefully regulated. If the temperature is too high, it may cause frequent side reactions and the product is impure; if the temperature is too low, the reaction rate will be slow and take a long time. The reaction time also needs to be accurately grasped. If it is too short, the reaction will not be fully functional, and if it is too long, it will cause the product to decompose or other adverse changes. The ratio of reactants is also related to success or failure. It is necessary to accurately mix according to the reaction mechanism and past experience to make the reaction smooth and efficient to obtain the 2-oxo-2,3-dihydro-1H-imidazole-4-carboxylate. And after each step of the reaction, it needs to be carefully separated and purified to remove impurities and obtain a pure product to meet the needs of subsequent use.
What are the applications of 2-oxo-2, 3-dihydro-1H-imidazole-4-carboxylate?
2-Oxo-2,3-dihydro-1H-imidazole-4-carboxylate, this compound has applications in many fields such as medicine, agriculture, and materials science.
In the field of medicine, it can be used as a key intermediate in drug synthesis. Because it contains a specific functional group structure, it can construct complex drug molecules through chemical reactions. For example, when developing antiviral drugs, the compound can be modified to connect with other active groups to obtain specific antiviral active molecules. And because it has adaptability to certain receptors or enzymes in organisms, or has potential biological activity, it can be directly developed as a drug for the treatment of specific diseases. After pharmacological research and clinical trials, it is expected to become an innovative therapeutic drug.
In agriculture, it can be used to create new types of pesticides. Because it has inhibitory or killing effects on certain pests or pathogens, it can be reasonably designed and modified to develop high-efficiency and low-toxicity pesticides. For example, for specific agricultural crop diseases, design fungicides containing this compound to protect the healthy growth of crops, reduce the use of chemical pesticides, and reduce environmental pollution.
In the field of materials science, you can participate in the preparation of functional materials. Because of its special chemical structure, it can endow materials with unique properties. For example, when synthesizing polymer materials, it is introduced into the polymer chain to change the solubility, thermal stability, and mechanical properties of the materials. Or it can be used to prepare intelligent responsive materials, which undergo structural changes according to changes in the external environment (such as temperature and pH value), so that the material exhibits different properties and has potential application value in sensors, drug controlled release carriers, etc.
In summary, 2-oxo-2,3-dihydro-1H-imidazole-4-carboxylate has important applications in many fields, and its application prospects will be broader with the development of science and technology.