1,3,4,6-tetraacetyltetrahydroimidazo[4,5-d]imidazole-2,5(1H,3H)-dione

This is a question about the chemical structure, which involves the chemical structure of a specific compound. However, the information given is a little complicated and special, and it needs to be further sorted out in order to clarify its exact meaning.
According to the description of the "1%2C3%2C4%2C6+-+%E5%9B%9B%E4%B9%99%E9%85%B0%E5%9F%BA%E5%9B%9B%E6%B0%A2%E5%92%AA%E5%94%91%E5%B9%B6%5B4%2C5+-+d%5D%E5%92%AA%E5%94%91+-+2%2C5%281H%2C3H%29-%E4%BA%8C%E9%85%AE%E7%9A%84%E5%8C%96%E5%AD%A6%E7%BB%93%E6%9E%84" given, it can be analyzed step by step.
It mentions "tetraethylbenzo tetrahydroquinolo [4,5 - d] quinoline", which is a fused ring compound. "2,5 (1H, 3H) -dione" indicates that there is a hydrogen atom in the 1H and 3H states at the 2nd and 5th positions, respectively, with a dione structure.
The structure of this compound is based on benzotetrahydroquinoline as the basic skeleton, and four ethyl groups are connected to the 1, 3, 4, and 6 positions of the benzotetrahydroquinoline ring. At the same time, the [4,5-d] quinoline part fused with benzotetrahydroquinoline is a ketone carbonyl at the 2nd and 5th positions, and there is 1 hydrogen (1H) on the carbon attached to the carbonyl at the 2nd position, and 3 hydrogens (3H) on the carbon attached to the carbonyl at the 5th position.
In summary, the chemical structure of this "1% 2C3% 2C4% 2C6-tetraethylbenzotetrahydroquinolo [4,5-d] quinoline-2,5 (1H, 3H) -dione" is based on a specific fused ring with a specific substituent and carbonyl structure.

1% 2C3% 2C4% 2C6 refers to a substance named tetraacetylhexaazaisowurtzane [4,5 - d] isowurtzane-2,5 (1H, 3H) -dione. This substance has a wide range of uses. In the aerospace field, it can be used as a high-energy propellant component. Due to its high energy properties, it can provide strong power for spacecraft, helping them break through many attractive forces and move towards the vast universe. In the military field, it can be used to make high-performance ammunition, enhance the explosive power and damage effect of ammunition, and play a key role in the battlefield. In terms of materials science, it can be used as a basic raw material for new energetic materials, laying the foundation for the development of energetic materials with special properties, and promoting the continuous development of materials science. Overall, this compound has crucial uses in the fields of aerospace, military, and materials science, serving as a key to opening new doors to development in a wide range of fields.

To prepare 2,5 (1H, 3H) -dione, the preparation method is as follows:
First take 1,3,4,6-tetraacetyl-tetrazabicyclo [4,5-d] imidazole-4,5-dione, which is the key raw material. Its preparation may require multiple steps of reaction, and the reaction conditions need to be carefully controlled.
First, the choice of raw materials needs to be carefully selected, and the purity and impurity content are all related to the final product. The choice of reaction solvent is also important. Different solvents have a great influence on the reaction rate and product purity, or suitable organic solvents can be selected, such as dichloromethane, N, N-dimethylformamide, etc., which can fully dissolve the reactants and promote the reaction.
Second, the control of reaction temperature and time is indispensable. If the temperature is too high, or the side reaction increases, the purity of the product decreases; if the temperature is too low, the reaction rate is slow and the reaction takes a long time. After many experiments, the optimal reaction temperature and time node should be explored.
Third, during the reaction process, a catalyst may be added to speed up the reaction rate and increase the yield. Choosing a suitable catalyst, such as some metal salts or organic bases, can reduce the activation energy of the reaction and make the reaction more likely to occur. < Br > After obtaining 1,3,4,6-tetraacetyl-tetrazabicyclo [4,5-d] imidazole-4,5-diketone, it is converted into 2,5 (1H, 3H) -diketone through specific reaction steps. This conversion step also pays attention to the reaction conditions, such as the regulation of pH. Peracid or peralkali environment may affect the reaction process and product structure. The pH of the reaction system can be precisely regulated by dropwise addition of suitable acid-base solution. After the reaction, the separation and purification of the product is also critical. Column chromatography, recrystallization, etc. can be used to remove impurities and improve the purity of the product to obtain high-purity 2,5 (1H, 3H) -diketone.

1% 2C3% 2C4% 2C6 refers to "tetraethylnitrile tetrahydroacridine base [4,5 - d] acridine-2,5 (1H, 3H) -dione", which is a class of organic compounds. Its physicochemical properties are quite important and are related to many applications in chemistry and related fields.
In terms of physical properties, this diketone compound is in a solid state at room temperature and pressure. Its melting point may be relatively high. Due to the interaction between molecules such as hydrogen bonds and van der Waals forces, the molecules are closely arranged, and high energy is required to disintegrate its lattice structure and melt. As for solubility, in view of the presence of polar groups in the molecule, it may have a certain solubility in polar solvents such as ethanol and acetone, while it may have a low solubility in non-polar solvents such as n-hexane.
From the perspective of chemical properties, the carbonyl group (diketone structural part) contained in this compound has typical carbonyl chemical properties. Carbonyl carbon atoms are positive and susceptible to attack by nucleophiles, and nucleophilic addition reactions can occur. For example, under the action of acidic catalysts with alcohols, or to form acetals or ketals. Furthermore, the nitrogen atom (acridine structural part) in the molecule has a certain alkalinity and can react with acids to form salts. This property is used in organic synthesis or for the separation and purification of this compound. In addition, its conjugated structure endows molecules with certain optical properties or fluorescence properties, which may have potential applications in optoelectronic devices, fluorescent probes and other fields.

What I am asking you is about the market price of 1% 2C3% 2C4% 2C6-tetraethylamidinyl tetrahydropyrrolio [4,5-d] pyrrole-2,5 (1H, 3H) -dione. These things are rarely known by ordinary people, but they may be specific chemicals and are not common in the market.
If you want to know its price, you must carefully consider its origin, difficulty in preparation, wide and narrow use, and the situation of supply and demand. If its preparation is complicated, rare raw materials are required, and its use is quite specialized, it can only be used in a specific field. On the contrary, if the preparation is relatively easy, the raw materials are common, and the demand is limited, the price may be inexpensive.
It is difficult to find the exact price. To get an accurate number, you can visit the market for chemical trading, ask the merchants who specialize in this industry, or consult the relevant transaction records and industry information, so as to get clues to its market price. Don't take unfounded words lightly, but rely on empirical evidence to get the truth.