1h Benzimidazole 5 Difluoromethoxy 2 3 4 Dimethoxy 2 Pyridinyl Methyl Sulfinyl Sodium Salt Hydrate 2 3
Quinoline Thiophene Imidazole Thiazole
1H-Benzimidazole, 5-(difluoromethoxy)-2-(((3,4-dimethoxy-2-pyridinyl)methyl)sulfinyl)-, sodium salt, hydrate (2:3)
Chemical Name 1H-Benzimidazole, 5-(difluoromethoxy)-2-((3,4-dimethoxy-2-pyridinyl)methyl)sulfinyl-, sodium salt, hydrate (2:3)
FAQ

What is the chemical structure of 1H-Benzimidazole, 5- (difluoromethoxy) -2- (((4-dimethoxy-2-pyridinyl) methyl) sulfinyl) -, sodium salt, hydrate (2:3)?

This is the chemical name of pantoprazole sodium hydrate. However, it is quite difficult to describe its chemical structure in ancient words, because the ancients did not have modern chemical knowledge and expression system. However, try to describe it in quaint language.

This compound contains a base of 1H-benzimidazole, and its 5 positions are connected with a difluoromethoxy group, which is similar to a difluorine and methoxy group. The 2 positions are connected with a complex group, which is connected with a ((3,4-dimethoxy-2-pyridyl) methyl) sulfinyl group. In addition, this compound is a sodium salt and contains crystal water in a ratio of 2:3.

If we speculate in the ancient sense, benzimidazole can be regarded as a core "ring body", and the difluoromethoxy group attached to the top 5 positions is like a branch of the ring body, which is formed by difluorine and methoxy. The two-position (3,4-dimethoxy-2-pyridyl) methyl) sulfinyl group, like a more complex "side branch", is connected by the pyridine ring body, modified by dimethoxy group, and then connected by methyl group, and then connected with sulfinyl group, attached to the side of the benzimidazole ring body. The state of sodium salt is like this "ring body branch" structure combined with sodium element, and crystalline water is like a moist "water droplet" attached to it, which exists in a ratio of 2:3. Although it is difficult to accurately describe the subtlety of modern chemical structures in ancient sayings, I will briefly imitate it.

What are the main uses of 1H-Benzimidazole, 5- (difluoromethoxy) -2- (((4-dimethoxy-2-pyridinyl) methyl) sulfinyl) -, sodium salt, hydrate (2:3)?

This is called 5- (difluoromethoxy) -2 - (((3,4-dimethoxy-2-pyridyl) methyl) sulfinyl) -1H-benzimidazole dihydrate disodium salt. It has a wide range of uses and is often used as a proton pump inhibitor in the field of medicine.

In the stomach, the proton pump of the lysine cells that secrete gastric acid. This substance can be specifically combined with a specific part of the proton pump, and the proton pump is irreversibly suppressed by the action of covalent bonds. As a result, the parietal cells are difficult to secrete hydrogen ions into the gastric cavity, and the secretion of gastric acid is effectively suppressed.

Therefore, this substance is mostly used to treat diseases related to gastric acid, such as gastric ulcers. The cause of gastric ulcers is often related to the erosion of gastric mucosa by excessive gastric acid. Treating with this product can reduce the concentration of gastric acid, reduce the irritation and erosion of gastric acid on the ulcer surface, and create favorable conditions for the healing of ulcers. Such as duodenal ulcers, which are also caused by abnormal gastric acid secretion, this product can also play an effect. In addition, patients with reflux esophagitis can stimulate the esophagus due to acid reflux, causing inflammation. The application of this substance can reduce acid reflux and relieve symptoms of esophageal inflammation.

In conclusion, 5- (difluoromethoxy) -2 - (((3,4-dimethoxy-2-pyridyl) methyl) sulfinyl) -1H -benzimidazole disodium salt is of great significance in the treatment of gastric acid-related diseases, and brings good news to many patients to relieve pain and restore health.

What are the physicochemical properties of 1H-Benzimidazole, 5- (difluoromethoxy) -2- (((4-dimethoxy-2-pyridinyl) methyl) sulfinyl) -, sodium salt, hydrate (2:3)?

This is the sodium salt of 5- (difluoromethoxy) - 2- (((3,4-dimethoxy-2-pyridyl) methyl) sulfinyl) - 1H-benzimidazole, hydrate (2:3). Its physical properties are quite important, related to its application in various fields.

Looking at its properties, under room temperature and pressure, or in a white to white powder shape, this form is easy to store and transport, and is also conducive to subsequent processing operations. Its solubility is also a key property. It may have a certain solubility in water, which makes it better dispersed and participated in the reaction in aqueous systems. However, the specific solubility may vary due to factors such as temperature and solution pH. In organic solvents, its solubility may vary depending on the type of solvent, like in some polar organic solvents, or show good solubility, while in non-polar solvents, the solubility is poor.

Melting point is also one of the important physical properties. The specific melting point temperature is a key indicator for identifying this substance, and it also has implications for temperature control during its preparation and processing. In terms of stability, under normal storage conditions, if extreme environments such as light, high temperature, and high humidity can be avoided, it can be relatively stable. However, when encountering special chemical substances such as strong acids and alkalis, or chemical reactions occur, their structures and properties change.

The understanding of the above physical properties is of crucial significance for giving full play to the efficacy of this substance and optimizing its preparation, storage and application processes.

What is the synthesis method of 1H-Benzimidazole, 5- (difluoromethoxy) -2- (((4-dimethoxy-2-pyridinyl) methyl) sulfinyl) -, sodium salt, hydrate (2:3)?

This is a method for preparing 5- (difluoromethoxy) -2 - (((3,4-dimethoxy-2-pyridyl) methyl) sulfinyl) -1H-benzimidazole disodium salt. The method is as follows:
First take an appropriate amount of 3,4-dimethoxy-2-pyridyl methyl mercaptan and dissolve it in a suitable organic solvent, such as anhydrous ethanol or dichloromethane. This organic solvent needs to be pure and anhydrous so as not to interfere with the reaction.
Then, under stirring, slowly add 5- (difluoromethoxy) -1H -benzimidazole-2 -mercaptan, and the stirring must be uniform so that the two are in full contact.
Then, add an appropriate amount of alkali, such as sodium hydroxide or sodium carbonate. The amount of alkali needs to be precisely controlled to adjust the pH of the reaction system and promote the reaction to proceed in the direction of generating the target product.
During the reaction process, the temperature and reaction time need to be strictly controlled. The temperature should be maintained in a specific range, such as between 40 and 60 degrees Celsius, for about 2 to 4 hours, during which the reaction phenomenon should be closely observed.
After the reaction is completed, the reaction liquid is cooled to room temperature, and then separated and purified. Filtration, extraction, column chromatography, etc. can be used to remove impurities to obtain pure 5- (difluoromethoxy) -2 - (((3,4-dimethoxy-2-pyridyl) methyl) sulfinyl) -1H -benzimidazole.
Then dissolve this product in an appropriate amount of water, add a calculated amount of sodium hydroxide, and react to form a sodium salt. After that, by evaporation concentration, cooling and crystallization, 5- (difluoromethoxy) -2 - ((3,4-dimethoxy-2-pyridyl) methyl) sulfinyl) -1H -benzimidazole disodium salt crystals can be obtained. The entire process requires meticulous operation and attention to detail to ensure the purity and yield of the product.

What is the application prospect of 1H-Benzimidazole, 5- (difluoromethoxy) -2- (((4-dimethoxy-2-pyridinyl) methyl) sulfinyl) -, sodium salt, hydrate (2:3) in the market?

I think this "1H - Benzimidazole, 5- (difluoromethoxy) -2 - (((3,4 - dimethoxy - 2 - pyridinyl) methyl) sulfinyl) -, sodium salt, hydrate (2:3) " is the expression of chemical substances. In today's market, its application prospects are quite promising.

This substance may have unique effects in the field of medicine. Because of the way of medicine, precise molecular structures are often sought to treat diseases. Its special chemical structure may target specific disease targets and have potential therapeutic effects. Such as the development of new anti-ulcer drugs, or by virtue of its structural characteristics, it can regulate gastric acid secretion, repair gastric mucosa, and achieve the effect of treating gastric ulcer and duodenal ulcer.

In the chemical industry, it is also possible. Chemical industry, reaction characteristics of heavy substances. This substance may be used as a special catalyst, because its structure can affect the rate and direction of chemical reactions, help synthesize organic compounds with specific structures, and improve production efficiency and product quality.

In agriculture, it is also possible. Agriculture is related to the national economy and people's livelihood, and high-efficiency and safe products are required. If this substance can be used reasonably, it may be used as a new pesticide auxiliary agent to enhance the adhesion and permeability of pesticides, improve the efficacy of pesticides, and reduce the amount of pesticides, which is beneficial to the sustainable development of agriculture.

However, in order to give full play to its application prospects, it is still necessary for scientific researchers to explore in depth, clarify its nature and reaction mechanism, and through repeated experiments, to make it shine in various fields of the market and add luster to the well-being of mankind.