(butanoyloxy)methyl methyl (4R)-4-(2,3-dichlorophenyl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate

(Butyryloxy) methyl, methyl (4R) -4- (2,3-dichlorophenyl) -2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate, this is an organic compound. According to its name, its structure can be deduced according to the naming rules of organic chemistry.
Its main body is the skeleton of 1,4-dihydropyridine, and the two and six positions on the pyridine ring are connected with one methyl group, and the four positions are connected with (2,3-dichlorophenyl). The 3,5-dicarboxylic acid of this pyridine ring, one is estered with methyl and the other is estered with (butyryloxy) methyl, and has a specific configuration of (4R) at the 4 position, indicating that the carbon atoms at this position have a specific spatial orientation.
The structure of this compound is unique, and the structure of organic compounds is often closely related to its characteristics. This structure may endow it with specific physical and chemical properties, and may have unique uses and values in organic synthesis, pharmaceutical chemistry, etc. Its specific utility depends on its chemical properties and the chemical environment in which it is located.

(Butyryloxy) methyl, methyl (4R) -4- (2,3-dichlorophenyl) -2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate This substance has a wide range of uses. In the field of medicine, it is often the key raw material for the development of drugs for cardiovascular diseases. Because of its unique structure, it has a specific regulatory effect on the physiological function of the cardiovascular system, and can help develop drugs such as antihypertensive and antiarrhythmic drugs to protect human cardiovascular health.
In the field of organic synthesis, this substance can be used as an important intermediate due to its own chemical properties. Chemists can use various chemical reactions to modify and modify their structures to derive many organic compounds with different properties and uses, thereby enriching the "material library" of organic synthesis and promoting the progress of organic synthesis chemistry.
At the level of scientific research and exploration, this compound provides a key sample for in-depth exploration of the structure and activity relationship of dihydropyridine compounds. By studying its reaction mechanism and structure-activity relationship, researchers can gain insight into the essence of the action of these compounds, lay a theoretical foundation for the creation of new functional compounds, and lead scientific research to a more profound state.

(Butyryloxy) methyl, methyl (4R) -4- (2,3-dichlorophenyl) -2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate This substance has unique physical properties. Looking at its shape, at room temperature, it is mostly white to off-white crystalline powder, with delicate texture, like a natural dust. Under the sun, it shimmers faintly, and it seems to contain endless mysteries.
As for its melting and boiling point, the melting point is about a specific range. This value is its inherent property. It is like the soul brand of a thing, which makes it quietly transform from a solid state to a liquid state at a specific temperature, opening a different state; the boiling point is also correspondingly defined. This property is related to its transformation in a high temperature environment, and is the key to studying its change law.
Solubility is also an important physical property. In common organic solvents, it shows different degrees of affinity. In some organic solvents, it is like a wanderer returning home, can dissolve quickly, and fuses with the solvent to form a uniform and stable system; in other solvents, it shows a state of alienation and is difficult to dissolve. This difference in solubility is due to the difference in the interaction between its molecular structure and the solvent molecules. It is like everything in the world, and there are differences between relatives and solvents, and they all follow the inherent laws.
In terms of density, it has a unique value, which measures the mass of its unit volume, just like the weight of a person, and is its inherent symbol. With this density characteristic, in many practical application scenarios, it can be used to determine its position in the mixture, or used for separation and purification operations, just like in a complicated world, to find the coordinates for its positioning.

The preparation method of (butyryloxy) methyl, methyl (4R) -4- (2,3-dichlorophenyl) -2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylic acid esters is an important matter in chemical synthesis. The method is as follows:
First take a suitable starting material, such as a pyridine derivative with a specific substituent, which is the basis for synthesis. Take (4R) -4- (2,3-dichlorophenyl) -2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylic acid as the initial material, and the pyridine ring and surrounding substituents in its structure provide the framework for subsequent reactions.
Next, this starting material is esterified with a reagent containing butyryloxy methyl and methyl. In this reaction, it is necessary to precisely control the reaction conditions, such as temperature, solvent and catalyst. Too high or too low temperature may affect the reaction rate and product purity. Choose a mild organic solvent, such as dichloromethane or ethyl acetate, to create a suitable reaction environment. Add specific catalysts, such as concentrated sulfuric acid or p-toluenesulfonic acid, to accelerate the esterification process and promote the conversion of reactants to target products.
During the reaction process, the degree of reaction needs to be monitored in real time by means of thin layer chromatography or high performance liquid chromatography. When the reaction reaches the desired level, post-treatment is performed. Extract the reaction mixture with a suitable solvent to remove impurities. After column chromatography or recrystallization, high purity (butyryloxy) methyl and methyl (4R) -4- (2,3-dichlorophenyl) -2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate were obtained. This preparation method requires fine operation and strict control to obtain the ideal product.

(Butyryloxy) methyl, methyl (4R) -4- (2,3-dichlorophenyl) -2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate This material is related to safety and needs to be cautious.
Its chemical structure is unique, or it has potential chemical reactivity. In case of open flame or hot topic, there is a risk of combustion and explosion. When storing, be sure to keep away from fire and heat sources, store in a cool and ventilated warehouse, and store it separately from oxidants and acids. Do not mix storage to prevent accidental chemical reactions.
During use, the operator must strictly follow the operating procedures. It is recommended to wear a self-priming filter gas mask (full mask), a tape gas suit, and rubber gloves to prevent contact with the skin and inhalation, causing damage to the body. If you accidentally come into contact with the skin, you should immediately take off the contaminated clothes and rinse with a lot of flowing water; if you accidentally enter the eyes, you should immediately lift the eyelids, rinse with flowing water or normal saline, and seek medical attention in time.
At the same time, the transportation of this object also needs to be cautious. Before transportation, check whether the packaging container is complete and sealed. During transportation, make sure that the container does not leak, collapse, fall, or damage. It is strictly forbidden to mix with acids, oxidants, food and food additives. During transportation, it should be protected from exposure to sunlight, rain, and high temperature.