What is the chemical structure of 2-Naphthalenesulfonic Acid, 3,3 '- (Cyclohexylidenebis ((2-Methyl-4,1-Phenylene) -2,1-Diazenediyl)) Bis (4,6-Dihydroxy-, Sodium Salt (1:2))?
This is the chemical name of 2-naphthalenesulfonic acid, 3,3 '- (cyclohexylenebis ((2-methyl-4,1-phenylene) -2,1-diazenediyl)) bis (4,6-dihydroxy-, sodium salt (1:2)). To clarify its chemical structure, the following methods should be used to analyze it.
The core of this compound is naphthalenesulfonic acid structure. For naphthalenes, aromatic hydrocarbons with fused diphenyl rings also have sulfonic acid groups (-SO 🥰 H) attached to the second position of the naphthalene ring. This is the key group that imparts water solubility to the compound.
Looking at the part connected to the 3,3 'position again, "cyclohexadebis ((2-methyl-4,1-phenylene) -2,1-diazenediyl) ", where "cyclohexadeyl" is the remaining group after removing a hydrogen atom from the cyclohexyl group, which is connected to the subsequent structure by a double bond. " (2-methyl-4,1-phenylene) " means that the 1st and 4th positions of the phenyl ring have substituents, and the 2nd position is methyl. And "2,1-diazenediyl" indicates that two nitrogen atoms are connected by a double bond (-N = N), and thereby two (2-methyl-4,1-phenylene) are connected, and both are connected to the 3,3 'position of the naphthalene ring.
As for "bis (4,6-dihydroxy-) ", it means that there are hydroxyl groups (OH) at the specific positions (4 and 6 positions) of the above-mentioned connected structures.
Finally, "sodium salt (1:2) ", it means that the hydrogen ion in this compound is replaced by sodium ion, and the ratio of compound to sodium ion is 1:2.
In summary, this compound has a complex chemical structure, fusing various structural units such as naphthalene ring, sulfonic acid group, nitrogen-containing double bond, substituted phenyl group, hydroxyl group and sodium ion, and each part is related to each other, endowing the compound with unique chemical properties and potential applications.
What are the main uses of 2-Naphthalenesulfonic Acid, 3,3 '- (Cyclohexylidenebis ((2-Methyl-4,1-Phenylene) -2,1-Diazenediyl)) Bis (4,6-Dihydroxy-, Sodium Salt (1:2))?
2-Naphthalenesulfonic acid, 3,3 '- (cyclohexylenebis ((2-methyl-4,1-phenylene) -2,1-diazenediyl)) bis (4,6-dihydroxy-, sodium salt (1:2)), this substance has specific uses in industry, scientific research and other fields.
In industry, it is often used as a dye intermediate. The Gain structure contains naphthalene ring, sulfonic acid group and special azene structure, which endows it with the ability to participate in a variety of chemical reactions. It can be converted into various dyes with bright color and good stability through a series of organic synthesis steps. It is used in the textile printing and dyeing industry to dye fabrics with brilliant colors and meet people's needs for textile aesthetics.
In the field of scientific research, it can be used as a reagent for chemical research. With its unique chemical structure, it can participate in the study of specific organic reaction mechanisms, helping researchers gain in-depth insight into the effects of reaction processes and reaction conditions on the structure and properties of products, and providing important experimental basis for the development of organic chemistry theory. It can also be used in the field of materials science to develop new materials with special optical and electrical properties, such as the preparation of functional materials that respond to specific wavelengths of light, or to improve the electrical conductivity of certain materials.
In pharmaceutical research and development, although it is not a direct drug component, it can be used as a lead compound due to potential interactions with certain enzymes or proteins in organisms. By studying its interaction mode with biomacromolecules, researchers can design and synthesize more active and selective drug molecules, providing ideas and directions for the development of new drugs.
Is 2-Naphthalenesulfonic Acid, 3,3 '- (Cyclohexylidenebis ((2-Methyl-4,1-Phenylene) -2,1-Diazenediyl)) Bis (4,6-Dihydroxy-, Sodium Salt (1:2)) safe and harmful?
2-Naphthalenesulfonic acid, 3,3 '- (cyclohexenebis ((2-methyl-4,1-phenylene) -2,1-diazenediyl)) bis (4,6-dihydroxy-, sodium salt (1:2)) The safety of this substance is related to everyone's health and needs to be reviewed in detail.
Looking at this chemical substance, its composition is complex and its structure is special. However, there is no conclusive record of its safety in the books.
In the field of chemical industry, many such complex compounds may be potentially harmful. Or because of the characteristics of some of the groups, they can react with substances in the biological body, thus affecting physiological functions.
Although there is no definitive evidence that it is necessarily harmful, when it is unknown, it is prudent. During production and use, it is necessary to strictly abide by the procedures and take protection. If it is not handled properly, it may cause environmental pollution, or cause damage to the human body, such as irritating the skin, mucous membranes, and even potentially carcinogenic and teratogenic risks.
Therefore, although it is difficult to determine its absolute harm, it should be treated with caution before all its characteristics are clarified. Do not act rashly to avoid causing disasters.
What are the physicochemical properties of 2-Naphthalenesulfonic Acid, 3,3 '- (Cyclohexylidenebis ((2-Methyl-4,1-Phenylene) -2,1-Diazenediyl)) Bis (4,6-Dihydroxy-, Sodium Salt (1:2))?
This substance is called 2-naphthalenesulfonic acid, 3,3 '- (cyclohexylenebis ((2-methyl-4,1-phenylene) -2,1-diazenediyl)) bis (4,6-dihydroxy-, sodium salt (1:2)), and its physicochemical properties are as follows:
In view of this compound, its sodium salt state is common. In terms of solubility, sodium salts tend to exhibit better solubility in water. Due to their ionized structure, they can form strong interactions with water molecules, which is conducive to their dispersion and application in aqueous systems.
When it comes to stability, the diazene digroups and other parts present in the structure of the compound are sensitive to external conditions such as light and heat. When illuminated or heated, the diazene digroups may decompose or rearrange, which may affect the stability of the whole compound. However, the cyclohexen and naphthalenesulfonic acid groups in the molecule give it a certain degree of structural rigidity, which can maintain a relatively stable state under moderate conditions.
In terms of color, usually such compounds containing complex aromatic structures and azo groups show a certain color, or yellow to orange, etc. This is caused by the electron transition in the molecular structure absorbing visible light of specific wavelengths.
Melting point and boiling point, because the substance is a sodium salt, its melting point and boiling point will be different from the corresponding neutral organic matter. The existence of ionic bonds enhances the intermolecular force, resulting in an increase in the melting point. The boiling point is also affected by the strong interaction between molecules, and a higher temperature is required to make the molecules break free from each other and gasify.
Furthermore, in the field of organic synthesis, it can participate in many reactions with naphthalene sulfonic acid groups, hydroxyl groups and other active check points, such as esterification with alcohols, or azo coupling reactions with diazene digroups, etc., showing unique chemical activity and reactivity. The many physicochemical properties of this compound lay the foundation for its application in dyes, drug synthesis and other fields.
2-Naphthalenesulfonic Acid, 3,3 '- (Cyclohexylidenebis ((2-Methyl-4,1-Phenylene) -2,1-Diazenediyl)) Bis (4,6-Dihydroxy-, Sodium Salt (1:2)) is produced?
This compound is called 2-naphthalenesulfonic acid, 3,3 '- (cyclohexylenebis ((2-methyl-4,1-phenylene) -2,1-diazenediyl)) bis (4,6-dihydroxy-, sodium salt (1:2)), and its preparation method is as follows:
To prepare this product, first take an appropriate amount of 2-naphthalenesulfonic acid raw material and prepare it carefully. Then a specific process is used to react 3,3 '- (cyclohexylenebis ((2-methyl-4,1-phenylene) -2,1-diazenediyl)) bis (4,6-dihydroxy-compound with it. During the reaction, the temperature, duration and ratio of the reactants should be carefully controlled. If the temperature is too high or too low, it may cause deviations in the reaction, affecting the purity and yield of the product.
The reaction vessel should be a vessel with good texture and can withstand the reaction conditions. The stirring process should also be smooth and continuous, so that the reactants can be fully mixed to facilitate the uniform progress of the reaction. When the reaction is coming to an end, according to the specific chemical method, slowly add an appropriate amount of sodium salt to make a ratio of 1:2. During this process, close attention should be paid to the phenomenon of the reaction, such as the change of color, the formation of precipitation, etc.
After the reaction is completed, use suitable separation and purification methods, such as filtration, crystallization, extraction, etc., to obtain a pure target product. Each step requires fine operation, and a little carelessness may cause the product to be mixed with impurities, resulting in a decrease in its quality. Therefore, after much effort and careful handling, we can obtain this 2-naphthalenesulfonic acid, 3,3 '- (cyclohexylenebis ((2-methyl-4,1-phenylene) -2,1-diazenediyl)) bis (4,6-dihydroxy-, sodium salt (1:2)) compound.
