3-ethyl 5-methyl 2-[(2-aminoethoxy)methyl]-4-(2-chlorophenyl)-6-methyl-1,4-dihydropyridine-3,5-dicarboxylate

This is the name of a chemical substance. According to its name, its chemical properties are quite unique. This substance contains the core structure of dihydropyridine, which is common in many drugs and is often closely related to specific physiological activities.
The presence of its substituents, ethyl, methyl, chlorophenyl, etc. has an impact on its physical and chemical properties. The introduction of ethyl and methyl can change the lipid solubility of compounds, making them different in solubility in different solvents. The existence of chlorophenyl can affect the electron cloud distribution of molecules due to the electron-absorbing properties of chlorine atoms, which in turn affects their chemical reactivity.
Furthermore, in this substituent, the amino group is alkaline and can react with acids to form salts. The presence of ethoxy groups may increase the hydrophilicity of molecules and improve their solubility in water.
In the structural part of 1,4-dihydropyridine-3,5-dicarboxylic acid esters, the chemical properties of ester groups are relatively active. Under certain conditions, hydrolysis reactions can occur to generate corresponding carboxylic acids and alcohols. This hydrolysis reaction is easier to carry out in acidic or alkaline environments.
This chemical substance exhibits unique chemical properties due to the interaction of various substituents, and may have potential application value in the fields of organic synthesis and drug development. Its different properties provide a broad exploration space for related research.

3 - ethyl + 5 - methyl + 2 - [ (2 - aminoethoxy) methyl] - 4 - (2 - chlorophenyl) - 6 - methyl - 1,4 - dihydropyridine - 3,5 - dicarboxylate, this is an organic compound with a wide range of uses.
In the field of medicine, this compound may have the potential to treat cardiovascular diseases. First, it may be a calcium channel blocker. It can reduce myocardial contraction and vasodilation by blocking calcium ions from entering myocardial and vascular smooth muscle cells, thereby reducing blood pressure and relieving angina symptoms. Second, it may also have a regulatory effect on arrhythmias. It may affect the electrophysiological characteristics of cardiomyocytes, regulate heart rhythm, and restore normal heartbeat.
In the field of scientific research, this compound is an important research tool. Due to its specific chemical structure and activity, scientists can use it to explore intracellular calcium ion signaling pathways. By observing its impact on cell physiological functions, we can gain a deeper understanding of the key role of calcium ions in cell activities, such as cell proliferation, differentiation and apoptosis.
In the field of organic synthesis, this compound is a key intermediate and can be used to synthesize organic molecules with more complex structures. Chemists can modify its structure and introduce different functional groups to create compounds with novel properties and functions, providing more possibilities for new drug development, materials science and other fields. Its application in organic synthesis has greatly expanded the diversity of organic compounds and promoted the development of related fields.

3 - ethyl + 5 - methyl + 2 - [ (2 - aminoethoxy) methyl] - 4 - (2 - chlorophenyl) - 6 - methyl - 1,4 - dihydropyridine - 3,5 - dicarboxylate is a rather complex organic compound. The synthesis of this compound can follow the following method.
The selection of starting materials is critical. An appropriate pyridine derivative can be selected as the starting material, and this pyridine derivative should have an activity check point for subsequent reactions. For example, a specific substituent of pyridine is selected for subsequent introduction of other functional groups.
First, for the hydrogen atom on the pyridine ring, a halogenation reaction can be used to use a specific halogenated reagent to replace the hydrogen at a specific position on the pyridine ring with a halogen atom under suitable reaction conditions, such as a specific temperature and the presence of a catalyst, laying the foundation for the subsequent reaction. This step requires precise control of the reaction conditions to ensure the selectivity of the halogenated position.
Then, an etherification reaction is carried out. The compound containing hydroxyl groups reacts with halogenated alkanes under basic conditions to form an ether bond. In this compound, to form the partial structure of 2 - [ (2 - aminoethoxy) methyl], alcohols containing 2 - aminoethoxy can be selected to react with corresponding halogenated methyl pyridine derivatives. Basic reagents such as potassium carbonate can be selected for alkaline conditions, and the reaction can be heated in an organic solvent to promote the formation of ether bonds.
Furthermore, an arylation reaction is carried out. Using a palladium-catalyzed coupling reaction, 2 - chlorophenyl is introduced into the pyridine by reacting a halide of 2 - chlorophenyl with a pyridine derivative. This reaction requires the selection of suitable palladium catalysts, ligands, and suitable bases and solvents, and heating the reaction under the protection of inert gas to improve the yield and selectivity of the reaction.
For the formation of carboxyl ester groups, the esterification reaction between carboxylic acids and alcohols can be carried out under acid catalysis. The corresponding carboxylic acids and alcohols such as ethanol and methanol are heated and refluxed in the presence of acid catalysts such as concentrated sulfuric acid to generate 3-ethyl-5-methyl-1,4-dihydropyridine-3,5-dicarboxylate partial structures.
During the synthesis process, each step of the reaction needs to be separated and purified by means such as column chromatography and recrystallization to ensure the purity of the intermediate product, and then ensure the quality and yield of the final product. Fine regulation of the reaction conditions at each step is crucial for the successful synthesis of 3 - ethyl + 5 - methyl + 2 - [ (2 - aminoethoxy) methyl] - 4 - (2 - chlorophenyl) - 6 - methyl - 1,4 - dihydropyridine - 3,5 - dicarboxylate.

This compound is 3-ethyl-5-methyl-2-[ (2-aminoethoxy) methyl] -4- (2-chlorophenyl) -6-methyl-1,4-dihydropyridine-3,5-dicarboxylate. Its structure is complex and contains a variety of functional groups. It needs to be investigated in detail for safety reasons.
In terms of chemical properties, it contains a dihydropyridine structure, which has certain reductivity. It may react in an oxidizing environment, or cause stability to be affected, or even form new products, or have unknown toxicity. Functional groups such as aminoethoxy and chlorophenyl also participate in the reaction, change the chemical properties of compounds, and under specific conditions, produce harmful by-products.
In terms of biological activity, dihydropyridine compounds are mostly related to calcium channels. This compound may affect the function of cellular calcium channels and interfere with physiological processes such as cell signaling and muscle contraction. Although it may have medicinal potential, if used improperly, it may cause adverse reactions in the cardiovascular system, such as abnormal blood pressure and arrhythmia, etc., causing serious damage to the body.
Toxicological research is indispensable. Animal experiments are required to observe its acute, subacute and chronic toxicity. Acute toxicity or cause damage to the body such as liver, kidney and other organs, affecting its normal function; under long-term exposure, chronic toxicity or gene mutation, carcinogenesis and other serious consequences.
In addition, the stability, solubility and other physical properties of the compound are also related to its safety. If the stability is poor, it is easy to decompose and deteriorate; poor solubility, or it is difficult to absorb and metabolize in the body, accumulating toxicity.
In summary, the safety of this compound requires in-depth research in many aspects, and a comprehensive assessment of its latent risk is required to ensure the safety of use.

There is a product named 3-ethyl + 5-methyl + 2 - [ (2 - aminoethoxy) methyl] - 4 - (2 - chlorophenyl) - 6 - methyl - 1,4 - dihydropyridine - 3,5 - dicarboxylate. The market prospect of this product is related to many aspects.
From its properties, if this product has unique chemical properties, it can be used in the field of medicine, or it can become a key component of new drugs to treat specific diseases. If the symptoms are widespread, the demand will be prosperous and the future will be bright. In materials science, it may be able to help the research and development of new materials. If the materials it participates in synthesis have excellent properties, such as high strength and high stability, and are used in construction, aviation and other industries, the market will also be broad.
However, the market prospect is not only determined by its own nature. Market competition is also the key. If there are many competing products in this field with similar performance, in order to stand out, it needs to have unique advantages, such as low cost and convenient production. Without this advantage, the road to promotion may be full of thorns.
Furthermore, policies and regulations have a deep impact. In the pharmaceutical industry, the approval is strict. If this product is developed and produced in accordance with regulations and is allowed to enter the market, the market door can be opened. In the field of chemical materials, environmental regulations may affect its production and sales. Sustainable development can only be achieved if the production process meets environmental standards and there is no emission of harmful substances.
In summary, the market prospect of 3-ethyl + 5 - methyl + 2 - [ (2 - aminoethoxy) methyl] - 4 - (2 - chlorophenyl) - 6 - methyl - 1,4 - dihydropyridine - 3,5 - dicarboxylate depends on its own characteristics, competition situation and policy environment. By gaining insight into various factors and making good use of them, we are expected to open up a vast market.