What is the chemical structure of 1- (2,6-difluorobenzyl) -3- (6-methoxypyridazine-3-yl) -5-methyl-6- (4-nitrophenyl) thieno [2,3-d] pyrimidine-2,4 (1H, 3H) -dione

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The first word "1 - (2,6-diethylamino) " shows that this structure is connected with a group of 2,6-diethylamino at the first position of the main chain. "Diethylamino" is a group formed by two ethyl groups connected to the nitrogen atom. It is a common substituent in organic structures and has certain electronic effects and steric barriers.

Also says "3- (6-methoxy-3-group) ", but the expression of "3-group" here is not detailed, or it is an omission in writing. If this is a specific known group, and it is connected to 6-methoxy and this "3-group" at position 3, methoxy (-OCH) is the power supply group, which can affect the electron cloud distribution and reactivity of the molecule.

In addition, "5-methyl", that is, there is a methyl (-CH) substitution at position 5 of the main chain. The introduction of methyl groups can change the spatial structure and physicochemical properties of the molecule.

And "6- (4-oxobenzyl) quinolino [2,3-d] pyrimidine-2,4 (1H, 3H) -dione" is a complex fused ring structure. Quinolino [2,3-d] pyrimidine-2,4 (1H, 3H) -dione is formed by fusing the quinoline ring with the pyrimidine ring, and the positions 2 and 4 are carbonyl (forming a dione structure), and the position 6 is connected to the 4-oxobenzyl group. The 4-oxo benzyl group, that is, the counterposition of the benzyl group, has a carbonyl group, which endows the molecule with a unique conjugate system and reactivity.

Overall, the structure of this compound is complex, and the interaction of various groups affects its physical and chemical properties. Although the "3-group" expression is unclear and the structure is difficult to be precise, the general framework can be outlined according to the above analysis. The uniqueness of its structure may make it have potential research value and application prospects in the fields of organic synthesis and medicinal chemistry.

What are the physical properties of 1- (2,6-difluorobenzyl) -3- (6-methoxypyridazine-3-yl) -5-methyl-6- (4-nitrophenyl) thieno [2,3-d] pyrimidine-2,4 (1H, 3H) -dione

The name 1- (2,6-diethylamino) -3- (6-methoxybenzyl-3-yl) -5-methyl-6- (4-chlorobenzyl) imidazolo [2,3-d] pyrimidine-2,4 (1H, 3H) -dione, which is an organic compound and the like.

On its physical properties, it is generally as follows: It may be in a solid state, and this is the case for such organic heterocyclic compounds. Looking at its structure, it contains many aryl groups, alkyl groups and heterocyclic rings, and the intermolecular forces are complex. Its melting point is speculated according to the similar structure. When it is in a higher temperature range, due to the strong intermolecular forces, more energy is required to break the lattice.

As for solubility, it may have a certain solubility in polar solvents, such as ethanol and acetone. Because it contains heteroatoms such as nitrogen and oxygen, it can interact with polar solvent molecules to form hydrogen bonds. However, in non-polar solvents, such as n-hexane and benzene, the solubility may be limited. Because the molecule as a whole has a certain polarity, it has a weak interaction with non-polar solvent molecules.

And its density is slightly heavier than water. Due to the complex structure of carbon, nitrogen, oxygen, chlorine and other atoms in the molecule, the relative molecular weight is relatively large. And this substance may have a certain stability. However, when it encounters strong acids, strong bases, strong oxidizing agents, etc., the structure may be destroyed, and a chemical reaction occurs, causing physical properties to change. < Br >
These are all based on similar structural compounds. To accurately understand their physical properties, experimental determination is required.

What is the synthesis method of 1- (2,6-difluorobenzyl) -3- (6-methoxypyridazine-3-yl) -5-methyl-6- (4-nitrophenyl) thieno [2,3-d] pyrimidine-2,4 (1H, 3H) -dione?

To prepare 1 - (2,6 - diethylamino) - 3 - (6 - methoxybenzyl - 3 - yl) - 5 - methyl - 6 - (4 - chlorophenylmethyl) imidazolo [2,3 - d] pyrimidine - 2,4 (1H, 3H) - dione, the method is as follows:

First take an appropriate amount of raw materials, and place each reactant containing a specific substituent in a certain proportion in the reaction vessel. Among them, the proportions of 2,6-diethylamino-related reactants, 6-methoxybenzyl-3-yl-related reactants, 5-methyl-related reactants, and 4-chlorophenyl-methyl-related reactants need to be precisely controlled to ensure that the reaction proceeds smoothly.

Then, choose a suitable reaction solvent to fully dissolve the reactants to construct a homogeneous reaction system. The properties of the obtained solvent, such as polarity, boiling point, etc., have a great influence on the reaction rate and product purity, so careful selection is required.

Furthermore, the reaction temperature and time are regulated. If the temperature is too high or too low, it may cause the reaction to deviate from the expected path, or cause the reaction rate to be too slow and the side reactions to increase. Improper time control may either make the reaction incomplete, or overreact and destroy the product structure.

During the reaction process, a catalyst can be used in a timely manner to accelerate the reaction process and improve the reaction efficiency. The catalyst used should have high activity and selectivity, which can promote the priority of the target reaction without causing too many side reactions.

After the reaction is completed, the target product should be separated from the reaction mixture by suitable separation and purification methods, such as extraction, distillation, recrystallization, etc., to remove impurities and improve the purity of the product.

After many fine operations, the pure 1- (2,6-diethylamino) -3- (6-methoxybenzyl-3-yl) -5-methyl-6- (4-chlorophenylmethyl) imidazolo [2,3-d] pyrimidine-2,4 (1H, 3H) -dione product can be obtained. The whole process requires strict operation and fine regulation by the experimenter to achieve a good synthetic effect.

1- (2,6-difluorobenzyl) -3- (6-methoxypyridazine-3-yl) -5-methyl-6- (4-nitrophenyl) thieno [2,3-d] pyrimidine-2,4 (1H, 3H) -dione What are the application fields?

Eh! Now there are chemical fields, 1- (2,6-diethylphenyl) -3- (6-methoxypropyl-3-yl) -5-methyl-6- (4-pyridyl benzyl) imidazolo [2,3-d] pyrimidine-2,4 (1H, 3H) -dione, which is the best.

This compound, its application domain. In the field of chemical, or can be used as a precursor to new research. Due to its unique properties, or the ability to interact with specific biological targets, such as the active sites of certain enzymes, or the cellular pathway, it is expected to be used to treat specific diseases, such as anti-tumor substances, inhibit the proliferation of tumor cells and their apoptosis for the purpose of treatment; or it can be used for the treatment of diseases of God, or the release or reception activity of God.

It can be used in the field of materials science, because it has a specific air-type, or can be used in the research of semi-nuclear materials. It can control the performance and optical properties of materials, and is used in the manufacture of optical diodes (OLEDs), energy cells and other devices to improve their performance and efficiency.

In terms of productivity, it may also develop its value. Or it can be used as a new type of active ingredient, which can effectively prevent and treat diseases by virtue of its action on specific biological targets, and is relatively good, or has higher environmental friendliness.

As such, this compound has great potential in various fields such as engineering, materials, and engineering, and is awaiting further investigation and development.

What is the market prospect of 1- (2,6-difluorobenzyl) -3- (6-methoxypyridazine-3-yl) -5-methyl-6- (4-nitrophenyl) thieno [2,3-d] pyrimidine-2,4 (1H, 3H) -dione?

Looking at this question, I talked about the market prospect of 1- (2,6-diethylamino) -3- (6-methoxybenzyl-3-yl) -5-methyl-6- (4-pyridyl benzyl) imidazolo [2,3-d] pyrimidine-2,4 (1H, 3H) -dione. This is the field of fine chemistry. To understand its prospects, we should look at it from multiple ends.

The first end of demand. In the field of medicine, such compounds may have unique pharmacological activities and can be used as key intermediates in drug development. Nowadays, many difficult diseases are in urgent need of new drugs, and the demand for characteristic structural intermediates is increasing. If this compound can lay the foundation for innovative drugs, the market prospect will be vast. For example, in the research and development of anti-tumor and antiviral drugs, imidazolidopyrimidine compounds with specific substituents are often of concern. If this product is suitable for related research and development paths, its demand may increase.

Second look at the competition situation. The field of chemical synthesis is developing rapidly, and similar structural compounds may emerge in an endless stream. If others have better synthesis processes and lower costs, it will pose a threat to the market share of this compound. On the contrary, if this product has exquisite synthesis technology and high quality, it can take the lead in the competition. Furthermore, regulations and policies are also key. Pharmaceutical regulations are constantly improving, and the requirements for compound safety and Quality Standards are strict. If this product can comply with regulations and pass various certifications, it can enter the market and obtain development opportunities.

Review the impact of technological innovation. If the new synthesis technology can improve the synthesis efficiency of this product, reduce energy consumption and reduce pollution, it will definitely expand its market space. And the progress of analysis and detection technology can more accurately determine its purity and characteristics, helping it to find a place in the high-end market.

Overall, the market prospect of 1- (2,6-diethylamino) -3- (6-methoxybenzyl-3-yl) -5-methyl-6- (4-pyridyl benzyl) imidazolo [2,3-d] pyrimidine-2,4 (1H, 3H) -dione has both opportunities and challenges. Growth in demand is an opportunity for its development. However, factors such as competition, regulations and technological changes also need to be carefully addressed in order to move forward steadily in the market.