What is the chemical structure of (5-methyl-2-oxo-1,3-dioxol-4-yl) methyl.5- (2-hydroxypropan-2-yl) -2-propyl-3- [4- [2- (2H-tetrazol-5-yl) phenyl] phenyl] methyl] imidazole-4-carboxylate?

This is the chemical name of (5-methyl-2-oxo-1,3-dioxacyclopentene-4-yl) methyl 5- (2-hydroxypropane-2-yl) -2-propyl-3- [4- [2- (2H-tetrazole-5-yl) phenyl] phenyl] methyl] imidazole-4-carboxylic acid ester. Its chemical structure can be deduced as follows:

Looking at its name, the first (5-methyl-2-oxo-1,3-dioxacyclopentene-4-yl) methyl group, which is a specific group, consists of a ring system of 1,3-dioxacyclopentene, which is formed by connecting methyl at the 5th position, carbonyl oxygen at the 2nd position, and methyl at the 4th position. < Br >
Looking at 5- (2-hydroxypropane-2-group) again, it can be seen that the 5-position of the imidazole ring is connected with 2-hydroxypropane-2-group, which is an isopropanol-derived group, and the hydroxyl group is connected to the 2-position carbon of the isopropyl group.

There is also 2-propyl, that is, the 2-position of the imidazole ring is connected with propyl. < Br >
3 - [4- [2- (2H-tetrazole-5-yl) phenyl] phenyl] methyl], indicating that the third position of the imidazole ring is connected with a complex aryl methyl structure, which contains two benzene rings connected, and the second position of one benzene ring is connected with 2H-tetrazole-5-yl.

Finally, it is a 4-carboxylic acid ester, and the 4-position of the nemidazole ring is a carboxylic acid ester structure, which is connected with the (5-methyl-2-oxo-1,3-dioxacyclopentene-4-yl) methyl group at the beginning by an ester bond.

In summary, the chemical structure of this compound is composed of an imidazole ring as the core, which is connected with a variety of specific substituents, and each substituent is ordered according to the middle position of the name and the structure description.

What are the physical properties of (5-methyl-2-oxo-1,3-dioxol-4-yl) methyl.5- (2-hydroxypropan-2-yl) -2-propyl-3- [4- [2- (2H-tetrazol-5-yl) phenyl] phenyl] methyl] imidazole-4-carboxylate?

(5-Methyl-2-oxo-1,3-dioxacyclopentene-4-yl) methyl.5- (2-hydroxypropyl-2-yl) -2-propyl-3-[ [4- [2- (2H-tetrazolyl-5-yl) phenyl] phenyl] methyl] imidazole-4-carboxylic acid ester, its physical properties are very important, related to its application in many fields. < Br >
Its appearance is often a specific form, or a crystalline state, the texture is delicate, and it looks crystal clear. The color may be pure and white, or slightly dyed yellow, but they all have a unique luster, just like beautiful jade emitting a soft light.

Melting point is one of its key physical properties. This melting point is precisely determined. Under a specific temperature, this substance will change from solid to liquid, like ice and snow melting when warm. This melting point data is accurate, providing an important basis for its purification and identification. The solubility of

is also not to be underestimated. In a specific solvent, this substance may dissolve rapidly and blend seamlessly with the solvent, just like a fish entering water, without stagnation; or the solubility is poor, only partially soluble, such as sand and gravel in water, it is difficult to completely blend. The difference in solubility in different solvents has a profound impact on its preparation and use. The density of

is also a characterization of the physical properties of the substance. Its density has been scientifically measured and can be accurately known. This value reflects the compactness of the substance, such as the weight of stone and the light of wood, due to different densities. This density property plays an important role in the storage and transportation of substances.

The above physical properties are related to each other and together outline the unique physical features of (5-methyl-2-oxo-1,3-dioxane-4-yl) methyl.5- (2-hydroxypropyl-2-yl) -2-propyl-3- [4- [2- (2H-tetrazol- 5-yl) phenyl] phenyl] methyl] imidazole-4-carboxylate, which lays a solid foundation for its subsequent research and application.

What is the use of (5-methyl-2-oxo-1,3-dioxol-4-yl) methyl.5- (2-hydroxypropan-2-yl) -2-propyl-3- [4- [2- (2H-tetrazol-5-yl) phenyl] phenyl] methyl] imidazole-4-carboxylate?

(5-Methyl-2-oxo-1,3-dioxacyclopentyl-4-yl) methyl.5- (2-hydroxypropyl-2-yl) -2-propyl-3- [4- [2- (2H-tetrazole-5-yl) phenyl] phenyl] methyl] imidazole-4-carboxylic acid ester, which is an organic compound with complex structure and diverse functional groups.

Its use in the field of medicine may have potential pharmacological activity. Or as a drug intermediate, participate in the drug synthesis process, chemically modified and reacted, and converted into drugs with specific curative effects. For example, tetrazole groups are often used in drug design because they can mimic carboxyl groups, enhance the affinity of compounds with biological targets, and affect drug activity and selectivity.

In the field of organic synthesis, or used to construct more complex molecular structures, providing key structural units for synthetic chemistry. Its unique structure can be used in a variety of organic reactions, combined with other reagents, to expand molecular diversity, and create new organic materials or compounds with special properties.

It may also have potential applications in the field of materials science. It can be modified or combined with other materials to endow materials with special properties, such as biocompatibility, electrical conductivity, etc., for the development of new functional materials.

What is the synthesis method of (5-methyl-2-oxo-1,3-dioxol-4-yl) methyl.5- (2-hydroxypropan-2-yl) -2-propyl-3- [4- [2- (2H-tetrazol-5-yl) phenyl] phenyl] methyl] imidazole-4-carboxylate?

The synthesis of (5-methyl-2-oxo-1,3-dioxolane-4-yl) methyl 5 - (2-hydroxypropyl-2-yl) - 2-propyl-3 - [4 - [2 - (2H-tetrazole-5-yl) phenyl] phenyl] methyl] imidazole-4-carboxylic acid esters is a key exploration in the field of organic synthesis. The synthesis process is like a delicate ancient technique deduction.

The selection of starting materials is crucial. When using suitable nitrogen-containing heterocyclic compounds, benzene derivatives with specific substituents, etc. The first step is to construct an imidazole ring structure, through classical condensation reactions. For example, compounds containing amino and carbonyl groups, under specific acid-base catalysis conditions, are similar to the rigorous temperature of ancient processing medicinal pills, control the reaction temperature and duration, and make them condensate, ingeniously forming the prototype of imidazole rings.

Then, the key (5-methyl-2-oxo-1,3-dioxy-4-yl) methyl and 5- (2-hydroxypropyl-2-yl) substituents are introduced. This process requires precise selection of reaction reagents, such as using corresponding halogenated hydrocarbons or alcohol derivatives, and using the magic method of nucleophilic substitution reaction to precisely connect each group like tenon-mortise fit.

As for the introduction of the complex structure of 3- [[4- [2- (2H-tetrazol- 5-yl) phenyl] phenyl] methyl], benzene derivatives can be gradually modified by using palladium-catalyzed coupling reactions and other means, just like ancient skilled craftsmen carefully carved utensils, one after another to build connections between benzene rings, and then introduce tetrazolyl, and finally obtain the target product. The entire synthesis process requires fine control of the reaction conditions at each step, such as the choice of solvent and the amount of catalyst, which are all related to success or failure. Just like the excellence of ancient processes, the synthesis of this complex compound can be achieved.

(5-methyl-2-oxo-1,3-dioxol-4-yl) methyl.5- (2-hydroxypropan-2-yl) -2-propyl-3- [[4- [2- (2H-tetrazol-5-yl) phenyl] phenyl] methyl] imidazole-4-carboxylate What are the related pharmaceutical products?

(5-Methyl-2-oxo-1,3-dioxacyclopentene-4-yl) methyl-5 - (2-hydroxypropyl-2-yl) - 2-propyl-3 - [ [ 4 - [2 - (2H-tetrazole-5-yl) phenyl] phenyl] methyl] imidazole-4 - carboxylic acid esters related pharmaceutical products are the key to the field of medical pharmacy.

Looking at this chemical name, its structure is complex and must contain unique pharmacological activities. Related drug products are commonly found in the cardiovascular drug category. This chemical structure may be closely related to angiotensin II receptor antagonists.

Such as losartan, as a classic angiotensin II receptor antagonist, can selectively block the binding of angiotensin II to the receptor, thereby dilating blood vessels and lowering blood pressure. Its mechanism of action may be similar to (5-methyl-2-oxo-1,3-dioxacyclopentene-4-yl) methyl-5- (2-hydroxypropyl-2-yl) -2-propyl-3 - [ [ 4- [2- (2H-tetrazole-5-yl) phenyl] phenyl] methyl] imidazole-4 -carboxylic acid esters, all of which interact with receptors through specific chemical structures to exert pharmacological effects.

Another example is valsartan, which also acts on angiotensin II receptors and is effective in the treatment of hypertension, heart failure and other diseases. The structural characteristics of this chemical may provide ideas for the development of new angiotensin II receptor antagonists, which is expected to develop drug products with better efficacy and fewer side effects, bringing good news to patients with cardiovascular diseases.