What is the chemical structure of 2,9-bis (p-methoxybenzyl) anthra [2,1,9-def: 6,5,10-d'e'f '] diisoquinoline-1,3,8,10 (2H, 9H) -tetrone?

This is a complex organic compound whose chemical structure can be interpreted as follows:

The name of this compound is verbose and has a specific chemical nomenclature. "2,9 - bis (p - methoxybenzyl) anthra [2,1,9 - def: 6,5,10 - d'e'f '] diisoquinoline - 1,3,8,10 (2H, 9H) - tetrone" In "2,9 - bis (p - methoxybenzyl) ", there are two p-methoxybenzyl groups connected at positions 2 and 9. " Anthra [2,1,9 - def: 6,5,10 - d'e'f '] diisoquinoline "reveals that its core structure is formed by fusing anthracycline with diisoquinoline ring, and the specific numbering position determines the connection method of the ring and the fusing check point." 1,3,8,10 (2H, 9H) -tetrone "indicates that there are four carbonyl (-C = O) functional groups at positions 1, 3, 8, and 10 (where 2H and 9H indicate the position of a specific hydrogen atom).

As shown in the diagram, the core anthracycline structure is in the shape of a tricyclic connection. The diisoquinoline ring is fused to a specific position of the anthracycline, and the p-methoxybenzyl group connected to the second and ninth positions is connected to the main structure by the benzene ring. The methoxy group is connected to the methylene group, and the carbonyl group at positions 1, 3, 8, and 10 is connected to the main structure carbon by double bond oxygen. Thus, the chemical structure of this complex organic compound is formed.

What are the main uses of 2,9-bis (p-methoxybenzyl) anthra [2,1,9-def: 6,5,10-d'e'f '] diisoquinoline-1,3,8,10 (2H, 9H) -tetrone?

2%2C9-bis%28p-methoxybenzyl%29anthra%5B2%2C1%2C9-def%3A6%2C5%2C10-d%27e%27f%27%5Ddiisoquinoline-1%2C3%2C8%2C10%282H%2C9H%29-tetrone, this is a complex organic compound. Its main uses are quite extensive. In the field of scientific research, it is often used as an intermediate in organic synthesis. Due to its unique structure, it can participate in a variety of chemical reactions, enabling scientists to create novel and specific organic materials.

In the field of materials science, this compound may be used to develop new photoelectric materials. Because its molecular structure gives special optical and electrical properties, it may be applied to organic Light Emitting Diode (OLED), solar cells and other devices to improve their performance and efficiency.

In the field of pharmaceutical chemistry, it also has potential application value. After structural modification and optimization, it may exhibit biological activity and become a potential drug lead compound, opening up a new path for drug research and development. Scientists can explore the possibility of treating specific diseases by studying their interactions with biological targets.

With its unique structure and properties, this compound has important uses in many fields such as scientific research, materials science and medicinal chemistry, providing opportunities and possibilities for innovation and development in various fields.

What is the synthesis method of 2,9-bis (p-methoxybenzyl) anthra [2,1,9-def: 6,5,10-d'e'f '] diisoquinoline-1,3,8,10 (2H, 9H) -tetrone?

To prepare 2% 2C9 -bis (p-methoxybenzyl) anthrano [2% 2C1% 2C9 - def% 3A6% 2C5% 2C10 - d% 27e% 27f% 27] diisoquinoline - 1% 2C3% 2C8% 2C10 (2H% 2C9H) -tetraketone, the method is as follows:

Take the raw material of anthraquinone first, and carry out the reaction of benzylation under specific reaction conditions. Select the p-methoxy benzylation reagent, in a suitable solvent system, such as an aprotic organic solvent, and be catalyzed by alkali substances to control the temperature, reaction time and other factors, so that the benzyl group is selectively attached to the specific position of anthraquinone, to obtain the intermediate product containing benzyl.

Then, for this intermediate product, an appropriate cyclization reagent is used to guide the intramolecular cyclization reaction in an acid or base-catalyzed environment. This process requires precise control of the reaction conditions, rearrangement and cyclization of the molecular structure, and gradually construction of the core skeleton of the target product.

During the reaction process, thin-layer chromatography or high-performance liquid chromatography is often used to monitor the progress of the reaction and the purity of the product. After the reaction is as expected, the impurities are removed by separation and purification techniques, such as column chromatography, recrystallization, etc., to obtain a pure 2% 2C9-bis (p-methoxybenzyl) anthracene [2% 2C1% 2C9 - def% 3A6% 2C5% 2C10 - d% 27e% 27f% 27] diisoquinoline - 1% 2C3% 2C8% 2C10 (2H% 2C9H) -tetraketone. The whole process requires fine control of each reaction link, according to the characteristics of raw materials, reagent activity, and reaction parameters to obtain satisfactory yield and purity.

What are the physical properties of 2,9-bis (p-methoxybenzyl) anthra [2,1,9-def: 6,5,10-d'e'f '] diisoquinoline-1,3,8,10 (2H, 9H) -tetrone?

2% 2C9 - bis% 28p - methoxybenzyl%29anthra%5B2%2C1%2C9 - def% 3A6% 2C5% 2C10 - d%27e%27f%27%5Ddiisoquinoline - 1%2C3%2C8%2C10%282H%2C9H%29 - tetrone is an organic compound with unique physical properties. This compound is often in a solid state. Looking at its color, it is mostly white or almost white powder, like snow falling in the early winter, pure and delicate.

When it comes to the melting point, it is about a specific temperature range. This temperature is the critical point for its transition from solid to liquid state. The exact melting point value is of great significance for the identification and purification of this compound. Its solubility in organic solvents is also worthy of attention. In some organic solvents such as dichloromethane and chloroform, it shows certain solubility characteristics, just like fish swimming leisurely in water, which can be dispersed more evenly; however, its solubility in water is extremely poor, just like oil dripping in water, and it is difficult to blend.

Furthermore, the density of the compound is also an important physical property, and the specific density makes it unique in related operations and application scenarios. Its stability is also a key consideration. Under normal environmental conditions, it has relative stability, just like a calm person, who can resist the interference of common external factors and is not prone to significant chemical changes. However, under certain extreme conditions, such as high temperature, strong acid and alkali environments, the stability will be affected, or changes such as decomposition and deterioration will occur.

What is the market outlook for 2,9-bis (p-methoxybenzyl) anthra [2,1,9-def: 6,5,10-d'e'f '] diisoquinoline-1,3,8,10 (2H, 9H) -tetrone?

There is now a product named 2,9-bis (p-methoxybenzyl) anthracene [2,1,9-def: 6,5,10-d'e'f '] diisoquinoline-1,3,8,10 (2H, 9H) -tetraketone. The prospect of this substance in the market situation is actually a matter of concern to everyone.

This substance has a unique structure and may have potential uses in many fields such as chemical industry and medicine. However, its market prospect still needs to be carefully reviewed.

In the field of chemical industry, due to its special chemical structure, it can be used as a raw material for new materials to help develop novel polymers. If properly applied, it may be able to make breakthroughs in material properties, such as enhancing the stability and flexibility of materials. This may be a big opportunity to develop the market for new chemical materials.

As for the pharmaceutical field, its unique structure may endow it with a certain biological activity. Or it can be developed into new drugs after in-depth research and used to overcome some difficult diseases. However, the road of pharmaceutical research and development is full of thorns, and it needs to go through layers of rigorous experiments and approvals.

However, there are many variables in the future of the market. First, the complexity and cost of the synthesis process are really the key. If the synthesis method is cumbersome and expensive, large-scale production and marketing activities will be hindered. Second, the competition of similar alternative products should not be underestimated. If there are alternatives with similar functions and low cost on the market, it is not easy for this product to gain a place. Third, the orientation of policies and regulations has a great impact on its market prospects. In the pharmaceutical and chemical industry, strict supervision requires corresponding adjustments to policy changes, or the rhythm of R & D and production.

Although 2,9-bis (p-methoxybenzyl) anthracene [2,1,9-def: 6,5,10-d'e'f '] diisoquinoline-1,3,8,10 (2H, 9H) -tetraketone has potential value and prospects, it still needs to deal with many challenges in order to emerge in the market. After unremitting efforts and detailed planning, there is a promising future.