2-[(4-Hydroxy-9,10-Dioxo-9,10-Dihydroanthracen-1-Yl)Amino]-5-Methylbenzenesulfonic Acid

In order to understand the chemical structure of this substance, it is necessary to analyze its various parts in detail. Here mentioned "2 - [ (4-hydroxyl-9,10-dioxide-9,10-dihydroanthracene-1-yl) amino] -5-methylanthraquinone-5-sulfonic acid".
First look at the framework of anthraquinone, anthraquinone is a structure fused by three benzene rings, with a conjugated system and stable properties. Its 9 and 10 positions are connected with dioxy groups to form a specific oxidation state.
4-hydroxyl-9,10-dioxide-9,10-dihydroanthracene-1-group moiety, at the first position of anthraquinone, there is a substituent containing a hydroxyl group, which may affect its polarity and reactivity.
There is another 5-methyl group, and a methyl group is added to the 5 position of anthraquinone to change the molecular spatial structure and electron cloud distribution. The sulfonic acid group is also connected to the 5 position, and the sulfonic acid group has strong hydrophilicity, which greatly affects the solubility and acidity of the substance. The amino group is connected to the 2 position, which further changes the molecular electronic properties and reaction check point.
In summary, this compound takes anthraquinone as the core and is modified with different substituents, and each group affects each other, giving it unique physical and chemical properties.

2-%5B%284-%E7%BE%9F%E5%9F%BA-9, 10-%E4%BA%8C%E6%B0%A7%E4%BB%A3-9, 10-%E4%BA%8C%E6%B0%A2%E8%92%BD-1-%E5%9F%BA%29%E6%B0%A8%E5%9F%BA%5D-5-%E7%94%B2%E5%9F%BA%E8%8B%AF%E7%A3%BA%E9%85%B8%E6%9C%89%E5%93%AA%E4%BA%9B%E7%89%A9%E7%90%86%E6%80%A7%E8%B4%A8%3F This expression contains some chemically related irregular or difficult-to-understand combination expressions. The following is understood in a canonical manner, and attempts to answer it from a chemical point of view.
2 - [ (4-hydroxy-9,10-dioxide-9,10-dihydroanthracene-1-yl) amino] - 5 -methylanthraquinone sulfonic acid, this compound has the following physical properties:
1. ** Appearance and properties **: Usually, such compounds containing anthraquinone structure are mostly solid forms. Due to the presence of conjugated systems in the molecule, they may exhibit certain colors, such as yellow and orange. In ancient Chinese, "its shape is usually solid, and its color may be yellow or orange, due to the system of intra-molecular conjugation".
2. ** Solubility **: In view of the fact that there are both hydrophobic anthraquinone skeletons and hydrophilic sulfonic acid groups, amino groups, hydroxyl groups and other groups in the molecule. It should have a certain solubility in water, because the sulfonic acid group can form a strong interaction with water molecules; and it may also have good solubility in organic solvents such as ethanol and acetone, because the anthraquinone skeleton has a certain lipophilicity. "It is soluble in water because of the base of sulfonic acid; it is also soluble in organic solvents such as ethanol and acetone, and the lipophilicity of anthraquinone."
3. ** Melting point and boiling point **: Due to the existence of various forces between molecules, such as hydrogen bonds (hydroxyl groups and amino groups can be formed), van der Waals forces, etc., the melting point is relatively high. Under heating conditions, decomposition may occur first instead of boiling. "Its intermolecular forces belong to hydrogen bonds and van der Waals forces, so the melting point is quite high. When heating, it may be solved first and never boil."

2-%5B%284-%E7%BE%9F%E5%9F%BA-9%2C10-%E4%BA%8C%E6%B0%A7%E4%BB%A3-9%2C10-%E4%BA%8C%E6%B0%A2%E8%92%BD-1-%E5%9F%BA%29%E6%B0%A8%E5%9F%BA%5D-5-%E7%94%B2%E5%9F%BA%E8%8B%AF%E7%A3%BA%E9%85%B8%E7%9A%84%E4%B8%BB%E8%A6%81%E7%94%A8%E9%80%94%E6%98%AF%E4%BB%80%E4%B9%88%3F%2C this chemical substance is complex and irregular, it is difficult to know exactly what it refers to. However, from general chemical knowledge, if it is an organic compound, 2- [ (4-methoxy-9,10-dioxide-9,10-dihydroanthracene-1-yl) oxy] -5-methylbenzothiophene-4-carboxylic acid, its main use may involve the following aspects:
In the field of organic synthesis, it can be used as a key intermediate to construct more complex organic molecular structures. Due to its unique chemical structure, it can undergo substitution, addition and other reactions with other organic reagents through specific chemical reactions, laying the foundation for the synthesis of organic materials with specific functions.
In materials science, it may be used to prepare optoelectronic materials. The conjugate structure in the molecule and the specific substituent make it have certain optoelectronic properties, which are expected to be applied to optoelectronic devices such as organic Light Emitting Diode (OLED) and organic solar cells to improve the luminous efficiency and charge transport performance of the device.
In pharmaceutical chemistry, it may have potential biological activity. Some compounds with similar structures have been found to have certain affinity for certain biological targets, and may be used as lead compounds for further structural modification and optimization to develop drugs for treating specific diseases. However, this needs to be verified by a large number of biological experiments.
However, due to the failure to clarify its exact structure and properties, the above uses are only speculations based on common similar structural compounds.

To prepare 2- [ (4-hydroxy-9,10-dioxy-9,10-dihydroanthracene-1-yl) amino] -5-methylanthraquinone sulfonic acid, the method is as follows:
First, react with 4-hydroxy-9,10-dioxy-9,10-dihydroanthracene-1-amine with appropriate reagents. Take an appropriate amount of 4-hydroxy-9,10-dioxide-9,10-dihydroanthracene-1-amine, place it in a clean reactor, add a suitable solvent, such as dimethylformamide, and stir to disperse it uniformly. Then, slowly add an acylating agent, such as acetyl chloride, and control the reaction temperature at 50-60 degrees Celsius, because this temperature range can promote the smooth progress of the reaction and reduce the occurrence of side reactions. During the reaction, closely monitor the reaction process, which can be tracked by thin-layer chromatography. When the raw material point disappears, the reaction is basically completed. Next, the reaction solution is treated, diluted with an appropriate amount of water, extracted with an organic solvent such as ethyl acetate, and the organic phase is collected. After drying with anhydrous sodium sulfate, the solvent is removed by distillation under reduced pressure to obtain the preliminary product.
times, the above product is reacted with the related precursor of 5-methylanthraquinone sulfonic acid. Transfer the preliminary product to another reaction vessel, add 5-methylanthraquinone sulfonic acid precursor, such as 5-methylanthraquinone-2-sulfonic acid chloride, and add an acid binding agent, such as triethylamine, to neutralize the acid generated by the reaction and ensure that the reaction proceeds in a positive direction. The reaction temperature is maintained at 80-90 degrees Celsius, which helps to improve the After several hours of reaction, the reaction was also monitored by thin-layer chromatography. After the reaction was completed, the reaction liquid was cooled, the generated salt was filtered off, and the filtrate was separated and purified by column chromatography to obtain the target product 2- [ (4-hydroxy-9,10-dioxide-9,10-dihydroanthracene-1-yl) amino] -5-methylanthraquinone sulfonic acid. The whole process needs to strictly control the reaction conditions and pay attention to the standardization of operation in order to improve the purity and yield of the product.

2-%5B%284-%E7%BE%9F%E5%9F%BA-9, 10-%E4%BA%8C%E6%B0%A7%E4%BB%A3-9, 10-%E4%BA%8C%E6%B0%A2%E8%92%BD-1-%E5%9F%BA%29%E6%B0%A8%E5%9F%BA%5D-5-%E7%94%B2%E5%9F%BA%E8%8B%AF%E7%A3%BA%E9%85%B8%E5%9C%A8%E4%BD%BF%E7%94%A8%E8%BF%87%E7%A8%8B%E4%B8%AD%E9%A1%91%E9%A1%91%E6%9C%89%E5%A4%9A%E4%B8%8D%E5%8F%AF%E8%A7%86%E4%B9%8B%E5%A4%84%EF%BC%8C%E5%BF%85%E9%A1%BB%E6%B3%A8%E6%84%8F%E4%B8%8B%E5%88%97%E4%BA%8B%E9%A1%B9%EF%BC%9A
First, this substance is toxic. Although it is widely used, it must not be close to the skin, into the eyes, or touch the mouth to prevent the danger of poisoning. On the occasion of deployment and use, when preparing protective equipment, if accidentally contaminated, quickly rinse with a lot of water, and seek medical treatment.
Second, it is active and easy to react with many substances. It is necessary to check the objects in contact with it carefully to avoid co-placement or mixing with strong oxidants, reducing agents, acids, alkalis, etc., to avoid violent reactions, explosions, fires and other dangers.
Three, this substance may have an impact on the environment. The waste after disposal should not be disposed of at will, but should be disposed of in a proper way in accordance with relevant regulations to prevent soil pollution, water sources, etc., and protect the ecological balance.
Furthermore, storage should also be paid attention to. It should be placed in a cool, dry and well-ventilated place, away from direct sunlight and hot topic environment, and placed separately from other chemicals to prevent qualitative change caused by interaction.
At the end, the person must be professionally trained, familiar with its nature, usage, and attention, and operate according to the standard procedure. Untrained people should not move around, so as not to cause disasters.
Make 2-%5B%284-%E7%BE%9F%E5%9F%BA-9, 10-%E4%BA%8C%E6%B0%A7%E4%BB%A3-9, 10-%E4%BA%8C%E6%B0%A2%E8%92%BD-1-%E5%9F%BA%29%E6%B0%A8%E5%9F%BA%5D-5-%E7%94%B2%E5%9F%BA%E8%8B%AF%E7%A3%BA%E9%85%B8%E6%97%B6, and keep this number in mind to ensure safety and no risk of misuse.