Perhydroimidazo 4 5 D Imidazole 2 5 Dione
Quinoline Thiophene Imidazole Thiazole
Perhydroimidazo[4,5-d]imidazole-2,5-dione
Chemical Formula C4H6N4O2
Molecular Weight 142.12 g/mol
Appearance Solid (predicted)
Boiling Point Decomposes (predicted)
Melting Point Decomposes (predicted)
Solubility In Water Low solubility (predicted)
Pka Value No data found (assumed)
Logp Value -1.48 (predicted)
Density 1.62 g/cm³ (predicted)
Flash Point No data found (assumed)
FAQ

What is the chemical structure of Perhydroimidazo [4,5-d] imidazole-2,5-dione?

"Perhydroimidazo [4,5 - d] imidazole - 2,5 - dione" is the name of chemistry. To understand its chemical structure, it is necessary to study the principles of chemistry in detail.

The chemical structure is the arrangement and connection of atoms in the molecule. This "Perhydroimidazo [4,5 - d] imidazole - 2,5 - dione" has a core structure of two imidazole rings fused together and is in a fully hydrogenated state. The so-called fully hydrogenated means that the unsaturated bonds in the ring are all hydrosaturated.

In this structure, two imidazole rings are connected in a specific way to form a unique spatial configuration. Among them, 2,5-dione indicates the existence of a diketone structure at specific positions (2 and 5 positions) of the imidazole ring. This diketone structure has a significant impact on the properties of the whole molecule, such as reactivity and physical properties.

From the perspective of atomic connection, each atom is connected to each other according to the rules of chemical bonding, and atoms such as carbon, nitrogen, and oxygen are covalently bonded to maintain the stability of the molecule. Hydrogen atoms adhere to the corresponding positions according to the valence state requirements of each atom. The complexity and uniqueness of this structure make it a unique research value in the field of chemistry, or has potential applications in materials science, medicinal chemistry, etc.

What are the physical properties of Perhydroimidazo [4,5-d] imidazole-2,5-dione

Perhydroimidazo [4,5-d] imidazole-2,5-dione is an organic compound. This substance has some unique physical properties.

It is mostly solid at room temperature. Due to the relatively strong intermolecular forces, the molecules are closely arranged to form a stable structure. Looking at its melting point, it is about a certain temperature range, which reflects the energy required for the molecules to break free from the lattice binding. When heated to the melting point, the molecules are energized enough to overcome some of the intermolecular forces, and the substance then melts from the solid state to the liquid state.

In terms of solubility, it is better in polar solvents. Because of its molecular structure or polar groups, it interacts with polar solvent molecules through hydrogen bonds or other polar groups to dissolve. However, in non-polar solvents, the solubility may be poor due to the lack of such interactions.

Its density is also an important physical property. The density reflects the mass of the substance per unit volume, which is related to the degree of compactness and relative molecular weight of its molecules. If it is closely packed and the relative molecular mass is large, the density is higher.

In addition, the compound may have a specific crystalline form. The crystalline form is determined by the arrangement of molecules in the lattice, and different crystalline forms may affect its physical properties and chemical activities.

Its color is mostly colorless or white, which may be due to the weak absorption of visible light by the molecular structure and does not significantly absorb specific wavelengths of light, so it presents such colors.

Where is Perhydroimidazo [4,5-d] imidazole-2,5-dione used?

Perhydroimidazo [4,5-d] imidazole-2,5-dione, that is, perhydroimidazo [4,5-d] imidazole-2,5-dione, is useful in medicine, materials and other fields.

In the field of medicine, it has a unique chemical structure and can be used as a key intermediate in drug synthesis. Taking the development of new antibacterial drugs as an example, its architecture can precisely fit with specific bacterial targets, and achieve antibacterial effect by interfering with the normal physiological process of bacteria. Or in the creation of anti-cancer drugs, by regulating the key pathways of cancer cell proliferation, it shows potential anti-cancer activity and provides new ideas for solving cancer problems.

In the field of materials, its performance is unique. Introducing it into polymer materials can improve the thermal stability and mechanical properties of materials. For example, when preparing high-performance engineering plastics, adding this substance can maintain good shape and mechanical strength of plastics in high temperature environments, and has broad application prospects in industries with strict material performance requirements such as aerospace and automobile manufacturing. And because of its special structure, it can form strong interactions with other materials. When preparing composites, it can significantly enhance the interface bonding force of composites and improve the overall performance.

In the field of chemical synthesis, it is an important building block for the synthesis of complex organic compounds. Because of its unique reactivity of the double-ring structure, organic molecules with special functions can be constructed through various chemical reactions, injecting vitality into the innovation and upgrading of chemical products, and helping to develop more high-value-added fine chemicals.

What are the synthesis methods of Perhydroimidazo [4,5-d] imidazole-2,5-dione

Perhydroimidazo [4,5 - d] imidazole - 2,5 - dione, that is, perhydroimidazo [4,5 - d] imidazole - 2,5 - dione, can be synthesized as follows:

To obtain perhydroimidazo [4,5 - d] imidazole - 2,5 - dione, it can be achieved by multi-step reaction. The first step is to select suitable raw materials, such as nitrogen-containing heterocyclic compounds and carbonyl compounds. Under specific conditions, the condensation reaction is carried out with the amine group containing nitrogen heterocyclic ring and the carbonyl group of the carbonyl compound. This reaction requires temperature control, pressure control, and the selection of suitable catalysts, or the reaction rate can be accelerated and the reaction yield can be increased. < Br >
In the second step, the cyclization reaction is applied to the first product. By adjusting the pH and temperature of the reaction system, the intra-molecular ring formation is promoted. In this process, the molecular structure is rearranged to form the required imidazolo [4,5-d] imidazole basic skeleton.

Furthermore, the cyclization product is hydrogenated. With suitable hydrogenation reagents, such as hydrogen and suitable catalysts (such as palladium carbon, etc.), the unsaturated bond is hydrosaturated, and the final product is perhydroimidazolo [4,5-d] imidazole-2,5-dione.

During each step of the reaction, the product needs to be properly separated and purified to remove impurities, maintain the purity of the product in each step, and then improve the quality and yield of the final product. And the fine regulation of each step of the reaction conditions is very critical, which is related to the success or failure of the reaction and the characteristics of the product.

How stable is Perhydroimidazo [4,5-d] imidazole-2,5-dione?

The stability of Perhydroimidazo [4,5 - d] imidazole - 2,5 - dione is related to many factors, which is a complex chemical topic.

From the structure point of view, the ring structure of the compound gives it a certain stability. The atoms in the ring are closely connected by covalent bonds, forming a relatively stable framework. The rigid structure of the ring can reduce the degree of freedom of rotation in the molecule, making the molecular configuration stable, and it is not easy to deform or dissociate easily due to external forces.

However, its stability is also affected by environmental factors. In terms of temperature, high temperature may cause a sharp increase in molecular kinetic energy, and the vibration of covalent bonds intensifies. When the energy exceeds the bond energy threshold, the bond is at risk of breaking, and the stability plummets; while at low temperature, the molecular kinetic energy is limited, the movement is sluggish, and the stability is relatively improved. The properties of

solvents also have a significant impact. Polar solvents may form hydrogen bonds with the compound, electrostatic interactions, etc., which change the electron cloud distribution or increase or decrease the stability. The force between non-polar solvents and compounds is weak, which has little effect on their stability.

In addition, chemical reactivity is also related to stability. If there are highly active reagents around the compound, it is easy to react with it, resulting in structural changes and loss of stability.

The stability of Perhydroimidazo [4,5 - d] imidazole - 2,5 - dione is the result of the balance between structural characteristics and environmental factors. Only by carefully observing these factors can we accurately grasp the law of its stability change and apply it well in chemical research and related application fields.