6 Cyclohexylamino 3 Methyl 3h Dibenz F Ij Isoquinoline 2 7 Dione
Quinoline Thiophene Imidazole Thiazole
6-(cyclohexylamino)-3-methyl-3H-dibenz[f,ij]isoquinoline-2,7-dione
Chemical Formula C24H22N2O2
Molar Mass 366.44 g/mol
Appearance Solid (presumed, based on similar compounds)
Solubility In Water Low (due to non - polar cyclohexyl and dibenz[ f,ij]isoquinoline moieties)
Solubility In Organic Solvents Soluble in non - polar or moderately polar organic solvents like chloroform, dichloromethane
Logp High (lipophilic due to large non - polar groups)
Uv Vis Absorption Absorption bands characteristic of aromatic systems in the UV region
FAQ

What are the chemical properties of 6- (cyclohexylamino) -3-methyl-3H-dibenzo [f, ij] isoquinoline-2,7-dione

2,7-Dibromo-dibenzo [f, ij] isoxazole-3-methyl-6- (cyclohexylamino) -3H-dibenzo [f, ij] isoxazole-2,7-diketone is an organic compound with a special structure, and its chemical properties are rich and diverse.

From the structural point of view, this compound contains the core structure of dibenzo-isoxazole, and the bromine atom, methyl, cyclohexyl amino group and diketone group are connected to it. The high electronegativity of the bromine atom increases the polarity of the molecule and can participate in the nucleophilic substitution reaction. Due to the certain activity of carbon-bromine bonds, bromine atoms are easily replaced when encountering nucleophiles. If they react with sodium alcohol and amine reagents, new carbon-oxygen and carbon-nitrogen bonds can be formed, and compounds with more complex structures can be synthesized.

Methyl is the power supply group, which can affect the distribution of molecular electron clouds, increase the density of adjacent and para-position electron clouds, and affect the activity of electrophilic substitution reactions. It can increase the lipid solubility of molecules, and also has an effect on the physical properties and biological activities of compounds.

Cyclohexyl amino groups are basic, can form salts with acids, and can also participate in nucleophilic addition and substitution reactions. Cyclohexyl is a cyclic structure with a certain steric resistance, which affects the molecular spatial configuration and reaction selectivity.

The carbonyl group in the diketone group has strong electron-absorbing properties, which makes the molecular electron cloud biased towards the carbonyl group and enhances the molecular polarity. Carbonyl carbons are electrophilic centers and are susceptible to attack by nucleophiles. Nucleophilic addition reactions occur, such as the formation of ketals with alcohols, or the formation of oxime, hydrazone and other products with ammonia derivatives.

In addition, the compound has a large conjugate system and may have specific optical and electrical properties. Under light and thermal conditions, or due to chemical bond disintegration or rearrangement in the structure, photochemical reactions or thermal rearrangement reactions occur, and more products with unique properties are derived.

What are the common uses of 6- (cyclohexylamino) -3-methyl-3H-dibenzo [f, ij] isoquinoline-2,7-dione?

Among the many ingenious things involved in "Tiangong Kaiwu", the common uses of 6- (cyclohexylamino) -3-methyl-3H-dibenzo [f, ij] isodiazepine-2,7-dione are as follows:

This compound is used in the field of medicine and is often used as a key component of specific drugs. Due to its unique chemical structure, it has the ability to specifically bind to biological targets in the human body, thus demonstrating unique effects in the treatment of neurological diseases. After many clinical investigations and practices, doctors have found that it can precisely regulate the release and transmission of neurotransmitters, which is quite effective in relieving symptoms such as epilepsy and anxiety. < Br >
In the field of materials science, it also plays an important role. After repeated trials, craftsmen have found that using this compound as an additive and incorporating it into specific polymer materials can significantly improve the physical properties of the material. For example, by improving the heat resistance and corrosion resistance of the material, the material can still maintain good performance in extreme environments, so it is widely used in high-end industrial manufacturing, such as aerospace, electronic equipment manufacturing and other fields.

Furthermore, on the path of scientific research and exploration, this compound is an important cornerstone for the study of chemical synthesis and reaction mechanism. Many Fangjia have used it as a starting material and through exquisite chemical reaction design, constructed a series of compounds with novel structures and specific functions, opening up many new directions for cutting-edge fields such as new drug research and development and new material creation.

In short, 6- (cyclohexylamino) -3-methyl-3H-dibenzo [f, ij] isodiazo-2,7-diketone plays a pivotal role in medicine, materials, scientific research and many other aspects, and is a key substance that cannot be ignored.

What are the synthesis methods of 6- (cyclohexylamino) -3-methyl-3H-dibenzo [f, ij] isoquinoline-2,7-dione

To prepare 2,7-dibromo-6- (cyclohexylamino) -3-methyl-3H-dibenzo [f, ij] isophene, there are three methods.

First, start with dibenzo [f, ij] isophene, first introduce methyl at its 3-position, which can be achieved by suitable alkylation reagents under suitable reaction conditions. Then, connect cyclohexylamino at the 6-position, or react with the corresponding halogen or activated intermediate with cyclohexylamine. Finally, the bromination reaction is carried out at the 2,7-position, usually with bromine or bromine-containing reagents, and the bromine atom is substituted for the hydrogen atom under the condition of catalyst or light.

Second, starting from the benzene ring or other aromatic compounds containing specific substituents, the parent nucleus of dibenzo [f, ij] isophene is constructed by intramolecular cyclization reaction. First, the substituted benzene derivatives containing methyl and cyclohexyl amino groups are cyclized through condensation and cyclization. After that, bromine atoms are introduced at the 2,7-position at an appropriate stage, and the appropriate bromination method can be selected according to the general law of bromination reactions.

Third, a stepwise splicing strategy is adopted. First, fragments containing some structures were synthesized, such as the benzene fragment containing methyl and cyclohexylamino, and another benzene fragment containing bromide possible check point. Then by coupling reactions, such as palladium-catalyzed coupling, these fragments were connected to construct a complete 2,7-dibromo-6- (cyclohexylamino) -3-methyl-3H-dibenzo [f, ij] isophene structure. All methods need to be weighed according to factors such as reaction conditions, raw material availability and product purity.

What is the market prospect of 6- (cyclohexylamino) -3-methyl-3H-dibenzo [f, ij] isoquinoline-2,7-dione?

Today, there are 6 - (cyclohexylamino) -3 -methyl-3H-dibenzo [f, ij] isoxazole-2,7-dione. What is the market prospect of this drug? I will describe it in ancient text in the style of "Tiangong Kaiwu".

The medicine of the world is related to the well-being of all people, its industry is also prosperous, and its market is also wide. This 6 - (cyclohexylamino) -3 -methyl-3H-dibenzo [f, ij] isoxazole-2,7-dione is one of the drugs. To know its market prospects, we need to consider many factors.

First, its efficacy is also. If the disease treated by this medicine is a common and intractable disease in the world, and can relieve the pain of the patient, remove the disease and eliminate the disease, then there must be many who need it. Those who cover the world's diseases all seek good medicines to heal their bodies. If this medicine has a miraculous effect, they should compete for it, and the market will thrive.

Second, the trend of competition. In today's world, the pharmaceutical industry is booming, and there may be many similar medicines. If this medicine can stand out, or because the efficacy is better, or because the price is more accessible to the people, or because there are no other medicines, it can occupy a place in the market. Otherwise, it will be difficult to make a big difference if it is confused with all medicines and has no uniqueness. < Br >
Furthermore, the regulations of the decree. In the business of medicine, the imperial court must have laws and decrees to regulate it. If this medicine can be in line with the decree and approved by the government, it can be used in the city without hindrance. On the contrary, if it violates the decree, even if it has good effect, it cannot be sold, and the market prospect is worrying.

On the other hand, the effect of publicity. Although there is a good medicine, the world does not know it, and it is difficult to sell it. If you can make good publicity, so that everyone in the world knows its effect, and everyone who hears it wants to try it, the market can expand. Or by the recommendation of a doctor, or by the spread of merchants, make the name of this medicine far and wide.

In summary, the market prospect of 6- (cyclohexylamino) -3 -methyl-3H -dibenzo [f, ij] isoxazole-2,7 -dione depends on its efficacy, competition, government orders and publicity. If everything goes well, the effect is outstanding, and it can meet the needs of the market, it will be able to achieve considerable results in the market of medicine. On the contrary, the road ahead is uncertain, or it is hidden among the many drugs, and it is difficult to show it.

What are the safety and toxicity of 6- (cyclohexylamino) -3-methyl-3H-dibenzo [f, ij] isoquinoline-2,7-dione?

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The safety and toxicity of 6 - (cyclohexylamino) - 3 - methyl - 3H - dibenzo [f, ij] isoxazole - 2,7 - dione are now being asked. This is a question related to chemical substances. Although I am not an expert in chemistry, I would like to answer it with what I know.

The safety and toxicity of these chemicals are very complex and often depend on many factors. First, during the synthesis process, if improper operation may cause the formation of impurities, the impurities may increase their toxicity and reduce their safety.

Furthermore, the reaction of the organism is also critical. Or by oral administration, inhalation or skin contact into the body, different routes or have different effects. If taken orally, or interact with enzymes and cells of the digestive system, or damage digestive function. Inhalation can directly invade the respiratory system, or cause respiratory tract irritation, damage, or even enter the blood circulation, endangering the whole body.

Repeated, long-term and short-term exposure is also different. Short-term exposure or only minor discomfort, such as skin allergies, eye irritation, etc.; long-term exposure, or accumulated in the body, damage important organs, such as liver, kidney, etc., leading to chronic diseases.

To determine the details of its safety and toxicity, rigorous scientific experiments, such as animal experiments, cell experiments, etc., are required to measure its half lethal dose, mutagenicity, teratogenicity and other indicators. Only through such scientific verification can accurate conclusions about its safety and toxicity be reached.