Anthra (2,1,9-def: 6,5,10-d'e'f ') diisoquinoline-1,3,8,10 (2H, 9H) -tetrone, 2,9-bis (4-chlorophenyl) -2,9-bis (4-chlorophenyl) isoquino [4', 5 ', 6': 6,5,10] anthra [2,1,9-def] isoquinoline-1,3,8,10 (2H, 9H) -tetrone What is the chemical structure of

This is a very complex organic compound named, interpreted in modern chemical language, and its name is "2,9-bis (4-chlorophenyl) -isoquinoline [4 ', 5', 6 ': 6,5,10] anthrano [2,1,9-def] isoquinoline-1,3,8,10 (2H, 9H) -tetraketone". To clarify its chemical structure, it is necessary to interpret it from the names of each part.

"Anthra" indicates that this compound contains the basic skeleton of anthracene, which is an aromatic hydrocarbon with three fused benzene rings. "Isoquinoline" is also an important structural fragment, a heterocyclic ring containing nitrogen.

"2,9-Bis (4-chlorophenyl) " indicates that the 4-position connecting two 4-chlorophenyl, 4-chlorophenyl, that is, the benzene ring, is replaced by a chlorine atom at the 2-position and the 9-position.

"Isoquinoline [4 ', 5', 6 ': 6,5,10] anthrano [2,1,9-def] isoquinoline-1,3,8,10 (2H, 9H) -tetraketone" indicates the fusing mode and the position of the ketone group of each ring system. Among them, symbols such as "[4 ', 5', 6 ': 6,5,10]" and "[2,1,9 - def]" precisely define the fused check point. "1,3,8,10 (2H, 9H) -tetraketone" indicates the presence of a ketone group (C = O) at positions 1, 3, 8, and 10, and 2H and 9H represent the state of a specific hydrogen atom. The chemical structure of

is roughly as follows: the anthracene skeleton is used as the core, the isoquinoline ring is fused at a specific position, and the 4-chlorophenyl group is connected at positions 2 and 9, and the ketone group is distributed at positions 1, 3, 8, and 10. The atoms are connected in order according to the naming rules, forming the unique spatial structure and chemical form of this complex organic molecule.

Anthra (2,1,9-def: 6,5,10-d'e'f ') diisoquinoline-1,3,8,10 (2H, 9H) -tetrone, 2,9-bis (4-chlorophenyl) -2,9-bis (4-chlorophenyl) isoquino [4', 5 ', 6': 6,5,10] anthra [2,1,9-def] isoquinoline-1,3,8,10 (2H, 9H) -tetrone What are the physical properties of

This is a complex organic compound with unique physical properties. The appearance of the compound is often in a specific form, or crystalline, with a specific color, or colorless and transparent, or a slightly yellowish state. It looks like ice crystals or jade chips, refracting a unique light, and seems to contain a faint glow. Its melting point is quite high, and it needs a specific high temperature to cause it to turn from solid to liquid. This melting point is like its tough barrier, which requires strong thermal energy to break. And within a specific temperature range, its solid state is stable, and it is not afraid of ordinary temperature fluctuations.

Furthermore, the solubility of this compound is unique. In some organic solvents, such as some alcohols and ether solvents, it can be moderately dissolved, just like fish entering water, the molecules gradually melt into it, forming a uniform dispersion system; however, in water, it is extremely difficult to dissolve, just like the mutual exclusion of oil and water, it is difficult to blend. Its density is also different from that of common solvents, either heavier than water or lighter than some organic solvents, and it will be stratified according to density differences in the mixed system.

Its stability is also an important physical property. Under normal environmental conditions, it can maintain its own structural stability and does not easily react with common substances in the air such as oxygen and carbon dioxide. In case of specific strong oxidants or reducing agents, or under extreme temperature and pressure conditions, the structure will change and exhibit chemical activity changes. The physical properties of this compound make it potentially useful in organic synthesis, materials science and other fields, waiting for wise men to explore and explore.

Anthra (2,1,9-def: 6,5,10-d'e'f ') diisoquinoline-1,3,8,10 (2H, 9H) -tetrone, 2,9-bis (4-chlorophenyl) -2,9-bis (4-chlorophenyl) isoquino [4', 5 ', 6': 6,5,10] anthra [2,1,9-def] isoquinoline-1,3,8,10 (2H, 9H) -tetrone What is the use of

This is a very complex organic compound named 2,9-bis (4-chlorophenyl) isoquinoline [4 ', 5', 6 ': 6,5,10] anthracene [2,1,9-def] isoquinoline-1,3,8,10 (2H, 9H) -tetraketone. In the ancient times mentioned in "Tiangong Kaiwu", although there is no knowledge of this precise compound, its use can be inferred by analogy with the wisdom and experience of the ancients.

In ancient China, the consideration of material use was mostly derived from its characteristics and actual needs. In this compound, because of its complex structure, it may have unique physical and chemical properties.

If this thing is in ancient times, its color, shape or its decorative use. Ancient craftsmen often looked for things with unique colors and strange textures, which were used for decorative utensils and buildings to show off luxury and delicacy. If this compound has a bright color or special crystal shape, it can be applied as a pigment to ceramics and fabrics to add brilliant colors.

In terms of chemical properties, it may have potential reactivity. Ancient alchemy and pharmaceuticals often explored the changes between substances. If this thing can react with other things, or can be used to make pills, in order to prolong health, although the knowledge at that time was limited, but the spirit of exploration can be learned.

Furthermore, in agriculture and horticulture, ancient farmers paid attention to soil improvement and pest control. If this substance has a specific effect on soil microorganisms or pests, it can be used as a soil conditioner to improve soil quality and help crops grow; or as an insect repellent to protect crops from insect invasion. Although these are all speculations based on ancient thinking and needs, it can also show the extensive exploration of material uses by the ancients.

Anthra (2,1,9-def: 6,5,10-d'e'f ') diisoquinoline-1,3,8,10 (2H, 9H) -tetrone, 2,9-bis (4-chlorophenyl) -2,9-bis (4-chlorophenyl) isoquino [4', 5 ', 6': 6,5,10] anthra [2,1,9-def] isoquinoline-1,3,8,10 (2H, 9H) -tetrone What is the synthesis method of

To make this Anthra (2,1,9 - def: 6,5,10 - d'e'f ') diisoquinoline - 1,3,8,10 (2H, 9H) - tetrone, 2,9 - bis (4 - chlorophenyl) - 2,9 - bis (4 - chlorophenyl) isoquino [4', 5 ', 6': 6,5,10] anthra [2,1,9 - def] isoquinoline - 1,3,8,10 (2H, 9H) - tetrone, follow the following ancient method.

Take an appropriate amount of 4 - chlorophenyl related raw materials and prepare them carefully. In a delicate ratio, it is combined with specific nitrogen-containing heterocycles and anthracene-based raw materials. In a specially made kettle, the temperature should be precisely controlled, or slowly raised or stabilized, in order to achieve the best reaction state.

During this period, it is necessary to observe its color, smell its smell, and adjust its heat and reaction speed according to subtle changes. When the contents of the kettle show a specific color change, and after careful inspection, it is known that the reaction is moderate. The ancient method of filtration and analysis is used to divide the impurities and extract the essence.

Compound with a carefully prepared solvent to polyester the resulting impurities, so that the impurities are eliminated and the product is gradually purified. Then, through processes such as evaporation and condensation, the product is precipitated in an appropriate state. Then by grinding the method to make the particle size uniform, the finished Anthra (2,1,9 - def: 6,5,10 - d'e'f ') diisoquinoline - 1,3,8,10 (2H, 9H) - tetrone, 2,9 - bis (4 - chlorophenyl) - 2,9 - bis (4 - chlorophenyl) isoquino [4', 5 ', 6': 6,5,10] anthra [2,1,9 - def] isoquinoline - 1,3,8,10 (2H, 9H) - tetrone is obtained. The whole process requires the manufacturer to be in awe and abide by the rules of the ancient law to make this masterpiece.

Anthra (2,1,9-def: 6,5,10-d'e'f ') diisoquinoline-1,3,8,10 (2H, 9H) -tetrone, 2,9-bis (4-chlorophenyl) -2,9-bis (4-chlorophenyl) isoquino [4', 5 ', 6': 6,5,10] anthra [2,1,9-def] isoquinoline-1,3,8,10 (2H, 9H) -tetrone is a security risk

This is a chemical substance called 2,9-bis (4-chlorophenyl) isoquinolo [4 ', 5', 6 ': 6,5,10] anthrano [2,1,9-def] isoquinoline-1,3,8,10 (2H, 9H) -tetraketone. Regarding its safety risks, it is necessary to investigate in detail from multiple aspects.

Looking at all chemical substances, their safety often depends on toxicity, stability, reactivity, etc. In terms of toxicity, if this substance is cytotoxic, genetically toxic, etc., or serious to the health of the organism, such as causing mutation of biological cells, organ damage. Stability is also critical. If it is easily decomposed, volatilized, or released under normal conditions, it will increase the risk of environmental and human exposure. Those with high reactivity, or react violently with surrounding substances, causing the risk of fire and explosion.

However, according to this chemical name alone, it is difficult to determine its safety risk. To be sure, it is necessary to undergo professional experimental analysis, such as toxicology experiments, to measure its acute, subacute, and chronic toxic effects on experimental animals; stability experiments, to observe its changes under different temperature and humidity and light conditions; reactivity experiments, to explore its reaction characteristics with common substances.

Therefore, with this name alone, it cannot be asserted whether it has a safety risk. It is still necessary to rely on scientific experiments and professional assessments to know whether it is safe or not.