As a leading ethyl 2-amino-5-oxo-7-(propan-2-yl)-5H-chromeno[2,3-b]pyridine-3-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 ethyl 2-amino-5-oxo-7- (propan-2-yl) -5H-chromeno [2,3-b] pyridine-3-carboxylate
This is the question of "ethyl 2 - amino - 5 - oxo - 7 - (propan - 2 - yl) -5H - chromeno [2,3 - b] pyridine - 3 - carboxylate" to know its chemical structure. The name of this compound, according to the chemical nomenclature, "ethyl" is ethyl, indicating the presence of an ethyl group, which is a group derived from ethane. "2 - amino" refers to an amino group in the 2 position, and the amino group is a nitrogen-containing active group. "5 - oxo" indicates that the 5 position has a carbonyl group, which has a unique chemical activity. " 7- (propan-2-yl) "means the 7-position isopropyl group, which is a branched alkyl group derived from propane." 5H-chromeno [2,3-b] pyridine "reveals that this is a parent nucleus with a specific cyclic structure, composed of chromene and pyridine. Table 3 of" 3-carboxylate "is a carboxylic acid ester group.
In summary, the chemical structure of this compound contains ethyl, amino, carbonyl, isopropyl, chromene-pyridine parent nucleus and carboxylic acid ester group. The interaction of each group determines its chemical properties and reactivity. Although there is no visual diagram, its chemical structure outline can be roughly constructed according to the naming rules.
What are the main uses of ethyl 2-amino-5-oxo-7- (propan-2-yl) -5H-chromeno [2,3-b] pyridine-3-carboxylate
Ethyl + 2 - amino - 5 - oxo - 7 - (propan - 2 - yl) -5H - chromeno [2,3 - b] pyridine - 3 - carboxylate, that is, 2 - amino - 5 - oxo - 7 - isopropyl - 5H - chromono [2,3 - b] pyridine - 3 - ethyl carboxylate, which has a wide range of uses.
First, in the field of pharmaceutical research and development, it is often used as a key intermediate. Due to its unique chemical structure, it can participate in a variety of drug synthesis reactions. After ingenious modification and transformation, compounds with specific biological activities can be produced. It may have potential antibacterial, anti-inflammatory, and anti-tumor effects, paving the way for the creation of new drugs. For example, when synthesizing some targeted anti-cancer drugs, it can act as an important starting material and help build complex drug molecular structures.
Second, it is also useful in the field of materials science. Because it contains special groups, it may be integrated into polymer materials through polymerization reaction, giving the material unique optical and electrical properties. For example, it is used to prepare optical sensor materials, with its structure responding to specific substances or physical quantities, causing changes in the optical properties of the material, and achieving sensitive detection of specific targets.
Thirdly, in the field of organic synthetic chemistry, it is an important building block for the construction of complex heterocyclic compounds. Chemists can use its structural characteristics to derive a series of heterocyclic compounds with novel structures through various organic reactions, such as nucleophilic substitution, cyclization, etc., to expand the library of organic compounds and inject vitality into the development of organic synthetic chemistry.
In conclusion, ethyl + 2 - amino - 5 - oxo - 7- (propan - 2 - yl) -5H - chromeno [2,3 - b] pyridine - 3 - carboxylate has shown value and potential in many fields such as medicine, materials and organic synthesis, providing key support for technological innovation and development in related fields.
What is the synthesis method of ethyl 2-amino-5-oxo-7- (propan-2-yl) -5H-chromeno [2,3-b] pyridine-3-carboxylate
To prepare ethyl 2 - amino - 5 - oxo - 7 - (propan - 2 - yl) -5H - chromeno [2,3 - b] pyridine - 3 - carboxylate, the method is as follows:
First take the appropriate starting material, which may contain specific benzopyran and pyridine structural fragments. In the first step, the active benzopyran derivatives and pyridine reactants can be met under suitable reaction conditions by means of the common condensation reaction in organic synthesis chemistry.
This reaction requires careful selection of solvents, such as non-protic organic solvents, such as dichloromethane, N, N-dimethylformamide, etc., to create an environment conducive to the reaction. The reaction temperature is also crucial, or it can be adjusted between room temperature and moderate heating, or it needs to be controlled by water bath, oil bath and other temperature control means to maintain the temperature in a suitable range, such as 30 ° C to 80 ° C, depending on the specific reaction activity.
During the reaction, an appropriate amount of catalysts, such as some Lewis acid catalysts, can be added to accelerate the reaction process and improve the reaction rate and yield.
After the condensation reaction is completed and the preliminary product is obtained, it may need to be separated and purified. The column chromatography method can be used to select a suitable eluent with silica gel as the stationary phase, and the separation can be achieved according to the difference in the partition coefficient between the product and the impurities between the stationary phase and the mobile phase.
The separated product may require further functional group modification, such as the introduction of specific functional groups such as amino groups and carbonyl groups. For the introduction of amino groups, nucleophilic substitution reactions may be used, and amino-containing reagents are used to react with the product. The reaction conditions also need to be carefully regulated. Solvent, temperature, catalyst and other factors will affect the reaction effect.
After a series of reactions, separations and modifications, ethyl 2-amino-5-oxo-7- (propan-2-yl) -5H-chromeno [2,3-b] pyridine-3-carboxylate can be obtained. The whole process requires fine operation and strict control of the reaction conditions to obtain the ideal product.
What are the physical properties of ethyl 2-amino-5-oxo-7- (propan-2-yl) -5H-chromeno [2,3-b] pyridine-3-carboxylate
ethyl+2-amino-5-oxo-7- (propan-2-yl) -5H-chromeno [2,3-b] pyridine-3-carboxylate is an organic compound, and its physical properties are particularly important, which is related to the performance of this compound in various chemical processes and practical applications.
Looking at its properties, this compound often shows a specific state. Or crystalline, the crystal structure is regular and orderly, and the luster is unique. Its crystal form and lattice arrangement are determined by the interaction between molecules. This ordered structure affects its many properties, such as density. Due to the tight packing of molecules, the compound has a specific density value. This value is of great significance in operations such as material separation and mixing, and helps to judge its distribution and behavior in the system.
Melting point is also a key physical property. When heated to a specific temperature, the molecule is energized enough to overcome the lattice energy and solidifies into a liquid state. The melting point of the compound is specific, reflecting the strength of the intermolecular force. Strong forces require higher energy to destroy the lattice, and the melting point is higher; conversely, it is lower. The melting point can be used to determine the purity. The melting point of pure products is sensitive, the melting point of impurities is reduced and the melting range is wider.
The solubility cannot be ignored. In different solvents, its dissolution behavior varies. In polar solvents such as alcohols, or due to the formation of hydrogen bonds or dipole-dipole interactions between molecules and solvents, it dissolves; in non-polar solvents such as alkanes, the solubility may be poor due to molecular polarity differences. This solubility affects the choice of chemical reaction media, and is also related to drug release and absorption in pharmaceutical preparations.
In addition, the boiling point of the compound is also of characterization significance. The boiling point reflects the energy required to overcome intermolecular forces when a liquid is converted into a gas. Understanding the boiling point is helpful to select suitable conditions in separation processes such as distillation to achieve effective separation from other substances.
In summary, the crystal properties, density, melting point, solubility and boiling point of ethyl+2-amino-5-oxo-7- (propan-2-yl) -5H-chromeno [2,3-b] pyridine-3-carboxylate provide important basis for its chemical research and practical application.
Ethyl 2-amino-5-oxo-7- (propan-2-yl) -5H-chromeno [2,3-b] pyridine-3-carboxylate
Alas! This is ethyl 2 - amino - 5 - oxo - 7 - (propan - 2 - yl) -5H - chromeno [2,3 - b] pyridine - 3 - carboxylate, an organic compound. Looking at its market prospects, there are really considerable things.
In today's world, the field of pharmaceutical research and development has made rapid progress, and many new drugs need to be created urgently. The unique structure of this compound, or its potential biological activity, can provide an opportunity for the development of new drugs. The specific groups contained in its structure may interact with specific targets in organisms, showing efficacy in anti-inflammatory, anti-tumor, antibacterial and other aspects. < Br >
There are also opportunities in the field of materials science. It may be chemically modified and used as a synthetic raw material for special functional materials. For example, in the field of optoelectronic device materials, rational design and modification may endow the materials with unique optical and electrical properties, and then be applied to the preparation of new optoelectronic devices.
Furthermore, with the advancement of organic synthesis technology, the synthesis method of this compound may be continuously optimized, the cost is expected to be reduced, and the yield will be improved. This will promote its large-scale production and application, and expand the scope of industrial production and scientific research practice.
Of course, its marketing activities and applications still need to overcome many challenges. In the field of medicine, it needs to undergo rigorous pharmacological and toxicological experiments to prove its safety and effectiveness. In the application of materials, it also needs to deal with issues such as compatibility with other materials.
Although there are challenges, the prospects are broad. Over time, after unremitting research by scientific researchers, ethyl 2-amino-5-oxo-7 - (propan-2-yl) -5H-chromeno [2,3-b] pyridine-3 - carboxylate may shine in the fields of medicine and materials, contributing to human well-being.