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What is the chemical structure of 2- (morpholin-4-yl) ethyl 2- {[3- (trifluoromethyl) phenyl] amino} pyridine-3-carboxylate?
The chemical structure of this compound "2- (morpholin-4-yl) ethyl 2- {[3- (trifluoromethyl) phenyl] amino} pyridine-3-carboxylate", let me explain in detail.
According to its name, this is an organic compound. First of all, the pyridine part, pyridine is a six-membered nitrogen-containing heterocycle, in this compound, the 3-position of pyridine is connected with a carboxyl group, and it is connected to 2- (morpholin-4-yl) ethyl by esterification reaction, and the 2-position of this ethyl is connected to the 4-position of the morpholine ring. The morpholine ring is a six-membered heterocyclic ring containing nitrogen and oxygen, and has a unique structure.
Furthermore, the 2-position of the pyridine is connected to a nitrogen-containing amino group, and the other end of the amino group is connected to 3- (trifluoromethyl) phenyl, and the 3-position of the phenyl group has trifluoromethyl. This trifluoromethyl group has strong electronegativity, which affects the physical and chemical properties of the compound.
In summary, the chemical structure of this compound is composed of a pyridine ring, a morpholine ring, a phenyl group and its upper substituent, etc. Each part is connected to form a unique spatial structure, and each group interacts to endow the compound with specific chemical activities and properties.
What are the main uses of 2- (morpholin-4-yl) ethyl 2- {[3- (trifluoromethyl) phenyl] amino} pyridine-3-carboxylate?
2-% (morpholine-4-yl) ethyl 2- {[3- (trifluoromethyl) phenyl] amino} pyridine-3-carboxylate is an organic compound with a wide range of uses.
In the field of medicinal chemistry, it may have important medicinal potential. The structural properties of this compound may enable it to exhibit specific biological activities or be used as a lead compound for drug development. With appropriate modification and optimization, it is expected to develop therapeutic drugs for specific diseases, such as anti-cancer, anti-inflammatory or neurological diseases. Because it contains specific functional groups, it may interact with specific targets in organisms, thereby regulating physiological processes and achieving the purpose of treating diseases.
In the field of materials science, it may also have unique uses. In view of its structure containing special groups, it may endow materials with special properties. For example, it may be used to prepare functional polymer materials, by binding with polymer chains to change the solubility, thermal stability or optical properties of the material. Adding this substance to coatings, plastics and other materials may improve material properties, enhance their weather resistance, wear resistance, etc.
Furthermore, in the field of organic synthesis chemistry, it can be used as a key intermediate. With its structural activity check point, it can participate in a variety of organic reactions to construct more complex organic molecular structures. Chemists can use this compound to introduce other functional groups through reactions such as nucleophilic substitution and electrophilic addition to expand the structural diversity of organic molecules and provide an important basis for the synthesis of new organic compounds.
What is the synthesis of 2- (morpholin-4-yl) ethyl 2- {[3- (trifluoromethyl) phenyl] amino} pyridine-3-carboxylate?
To prepare 2- (morpholine-4-yl) ethyl 2- {[3- (trifluoromethyl) phenyl] amino} pyridine-3-carboxylic acid ester, the method is as follows:
First take 3- (trifluoromethyl) aniline and appropriate pyridine-3-carboxylic acid derivatives, such as 2-halogenated pyridine-3-carboxylic acid ester, with a suitable base as catalyst, in a suitable organic solvent, heated at controlled temperature, carry out nucleophilic substitution reaction. For bases, potassium carbonate, sodium carbonate and the like can be selected; for solvents, acetonitrile, N, N-dimethylformamide can be used. When reacting, pay close attention to the temperature and reaction process to ensure a smooth reaction.
After the first step is completed, the resulting intermediate is reacted with 2- (morpholine-4-yl) ethanol. This step also requires alkali catalysis and an appropriate solvent environment. The base can be replaced by a strong base such as potassium tert-butoxide, and the solvent can be selected as tetrahydrofuran. Temperature control allows it to fully react to form the target product 2 - (morpholine-4-yl) ethyl 2 - {[3 - (trifluoromethyl) phenyl] amino} pyridine-3-carboxylic acid ester. The
reaction is completed, and the product is purified by ordinary separation and purification methods, such as column chromatography, recrystallization, etc. During column chromatography, choose the appropriate silica gel and eluent; for recrystallization, choose the appropriate solvent to make the product pure, and obtain the required 2- (morpholine-4-yl) ethyl 2- {[3- (trifluoromethyl) phenyl] amino} pyridine-3-carboxylic acid ester.
What are the physical and chemical properties of 2- (morpholin-4-yl) ethyl 2- {[3- (trifluoromethyl) phenyl] amino} pyridine-3-carboxylate?
2-%28morpholin-4-yl%29ethyl 2-%7B%5B3-%28trifluoromethyl%29phenyl%5Damino%7Dpyridine-3-carboxylate, this is an organic compound. Looking at its structure, it contains groups such as pyridine, phenyl and morpholine groups, and the interaction of each group endows the compound with unique physical and chemical properties.
First of all, its solubility. Because the molecule contains both nitrogen heterocycles and amino groups with certain polarities, as well as hydrophobic groups such as trifluoromethyl, it may have a certain solubility in polar organic solvents such as methanol, ethanol, and acetonitrile, but its solubility in water may be limited. Because the polar part can form hydrogen bonds and other interactions with water molecules, the hydrophobic groups will hinder their dispersion in water.
When it comes to the melting point, the intermolecular forces are complex. There is π-π stacking between the aromatic rings, and the nitrogen atoms on the morpholine ring and the pyridine ring may participate in the formation of hydrogen bonds, which makes the intermolecular force enhanced and the melting point may be relatively high. However, the exact value needs to be accurately determined by experiments.
In terms of stability, the structure of the pyridine ring and the benzene ring is relatively stable. However, there are lone pairs of electrons on the nitrogen atom of the amino group, which are nucleophilic. In the presence of acidic or oxidizing agents, or the reaction may cause structural changes. Although trifluoromethyl is relatively stable, it may also participate in the reaction under certain strongly basic conditions.
As for volatility, because of its relatively large molecular mass and strong intermolecular force, volatility or weak. Under normal conditions, it is difficult to transition from liquid or solid to gaseous dissipation.
Overall, the physical and chemical properties of 2-%28morpholin-4-yl%29ethyl 2-%7B%5B3-%28trifluoromethyl%29phenyl%5Damino%7Dpyridine-3-carboxylate are determined by their unique molecular structures, and they behave differently in different environments. In-depth research on them will help to better apply in organic synthesis, drug development and other fields.
2- (morpholin-4-yl) ethyl 2- {[3- (trifluoromethyl) phenyl] amino} pyridine-3-carboxylate in the market price?
Today I have a question, what is the market price of 2 - (morpholin - 4 - yl) ethyl 2 - {[3 - (trifluoromethyl) phenyl] amino} pyridine - 3 - carboxylate. This is a fine chemical, and it is not easy to know its price. Because its price often changes for many reasons.
First, the cost of production has a great impact. The price of raw materials and the complexity of the preparation process are all key. If raw materials are scarce and difficult to find, the price must be high, and the price of this compound will also rise. If the preparation process is complicated, it requires multiple steps and special conditions, and the cost of manpower and material resources is high, and the price is not low.
Second, the supply and demand situation of the market is also the main reason. If there are many people who ask for it, and there are few people who supply it, the price will rise; on the contrary, if there is an excess supply, the demand will be weak, and the price will drop.
Third, the purity of the product also affects the price. High purity is more difficult to prepare, and the price will be higher; low purity is relatively cheap.
Fourth, the price varies depending on the supplier. Well-known large factories, due to factors such as brand, quality control, etc., the price may be higher than that of small factories.
However, after searching for ancient books, the exact price of this compound was not obtained. If you want to know the details, you can consult the chemical product supplier or the chemical product trading platform to obtain a more accurate price.