(8Z)-7-Oxo-8-(2-{4-[(E)-Phenyldiazenyl]Phenyl}Hydrazinylidene)-7,8-Dihydronaphthalene-1,3,6-Trisulfonic Acid - N-Cyclohexylcyclohexanamine (1:1)

The compound is named (8Z) -7-oxo-8- (2- {4- [ (E) -phenylhydrazinyl] phenyl} hydrazine fork) -7,8-dihydronaphthalene-1,3,6-trisulfonic acid-N-cyclohexylcyclohexylamine (1:1). In terms of structural analysis, the (8Z) -7-oxo-8- (2- {4- [ (E) -phenylhydrazinyl] phenyl} hydrazine fork) -7,8-dihydronaphthalene-1,3,6-trisulfonic acid part, the naphthalene ring as the core structure, there is an oxo group at the 7th position, and a more complex substituent containing benzene ring and hydrazine fork structure is connected at the 8th position, and the 1, 3, and 6 positions of the naphthalene ring are respectively connected with sulfonic acid groups. The N-cyclohexyl cyclohexylamine part is connected to the nitrogen atom of another cyclohexylamine by a cyclohexyl group. The whole compound is composed of the above two parts in a ratio of 1:1, or combined together through ionic bonds, hydrogen bonds, etc., to form a specific chemical structure. Such a structure makes it have unique physical and chemical properties and potential chemical activities, and may have specific uses in chemistry and related fields.

(8Z) -7-oxo-8- (2- {4- [ (E) -phenylhydrazinylphenyl} hydrazinido) -7,8-dihydronaphthalene-1,3,6-trisulfonic acid-N-cyclohexylcyclohexylamine (1:1), this is a specific chemical substance expression. It has a wide range of uses. In the field of dyes, it is often used as a reactive dye ingredient. By virtue of its complex chemical structure, it gives fabrics a lasting and bright color, and it has excellent dyeing fastness. After multiple washes and lighting, the color remains bright. In the field of analytical chemistry, due to its unique chemical properties, it can act as a special indicator. In a specific chemical reaction or analysis process, it can accurately indicate the reaction process or the existence of a specific substance with the help of color changes. In the field of materials science, it can be used as a functional additive and added to polymer materials to improve material properties, such as enhancing material stability and enhancing its adsorption capacity for specific substances. The diverse uses of this substance have provided important assistance for the development of many fields such as chemicals and materials, and are of great significance in promoting technological innovation and product optimization in related fields.

(The name of this compound is extremely complex and contains many professional chemical group descriptions. The following will be expanded from the perspective of general common chemical physical properties speculation) This is a compound formed by a specific structure of naphthalene derivatives and N-cyclohexyl cyclohexylamine in a 1:1 ratio. Generally speaking, organic compounds with such complex structures may have unique physical properties.
Looking at its structure, the naphthalene ring part imparts a certain rigidity and conjugation system, or makes it have a certain thermal stability, and the structure is relatively stable at higher temperatures. The presence of sulfonic acid groups will significantly enhance the hydrophilicity of the compound. Because sulfonic acid groups are very easy to form hydrogen bonds with water molecules, their solubility in water is good, or a homogeneous solution can be formed.
Furthermore, the nitrogen-containing part, such as the N-cyclohexyl cyclohexylamine part, will affect the intermolecular force. The cyclohexyl structure is relatively large, which increases the steric resistance of the molecule, which may affect the melting point and boiling point of the compound. Or because the intermolecular arrangement is hindered by space, the melting point is slightly lower than that of the same type of compounds without this large steric resistance.
And the azophenyl structure in it, because of its conjugate system, may respond to optical and electrical properties. Or under the irradiation of specific wavelengths of light, structural changes occur, which in turn affect the overall physical properties, such as color changes. However, the specific physical properties need to be accurately determined by experiments to determine their exact melting point, boiling point, solubility and other parameters.

To prepare (8Z) -7-oxo-8- (2- {4- [ (E) -phenyldiazenyl] phenyl} hydrazine fork) -7,8-dihydronaphthalene-1,3,6-trisulfonic acid-N-cyclohexylcyclohexylamine (1:1), the synthesis method is as follows.
First, the corresponding starting materials need to be prepared, such as compounds containing naphthalene rings, phenylhydrazine derivatives with specific substituents, and N-cyclohexylcyclohexylamine.
In an appropriate reaction vessel, an organic solvent is used as the medium, such as dichloromethane, N, N-dimethylformamide, etc., depending on the solubility of the reaction substrate. The starting material containing the naphthalene ring is put into it, and appropriate bases, such as potassium carbonate, sodium carbonate, etc., are added to adjust the pH of the reaction system, which is conducive to the subsequent reaction.
Slowly add phenylhydrazine derivatives with specific substituents. This process requires attention to the control of the reaction temperature, generally between low temperature and room temperature, such as 0 ° C - 25 ° C, to prevent side reactions from occurring. After the two are mixed evenly, the temperature can be appropriately raised to 40 ° C - 60 ° C, so that the reaction can be fully carried out, which lasts for several hours. During this period, the reaction process may need to be monitored by thin-layer chromatography. When the raw material point is basically eliminated, the reaction reaches the expected degree.
Then, the reaction solution is cooled to room temperature, an appropriate amount of water is added, and the product is extracted with an organic solvent. After drying the organic phase with anhydrous sodium sulfate, the organic solvent is removed by distillation under reduced pressure to obtain a crude product.
For the crude product, it can be purified by column chromatography. Silica gel is used as the fixed phase, and a suitable proportion of petroleum ether and ethyl acetate mixture is used as the mobile phase. The fractions of the target product are eluted and collected.
Finally, the product and N-cyclohexylcyclohexylamine in a ratio of 1:1, mixed in a suitable solvent, such as ethanol, acetone, etc., heated and stirred to fully react the two. After the reaction is completed, cool and crystallize, filter and dry to obtain (8Z) -7-oxo-8 - (2 - {4 - [ (E) -phenyldiazenyl] phenyl} hydrazine fork) -7,8 -dihydronaphthalene-1,3,6 -trisulfonic acid-N-cyclohexylcyclohexylamine (1:1) product. During the whole process, it is necessary to strictly control the reaction conditions and operate carefully to obtain the ideal product.

(8Z) - 7-oxo-8- (2 - {4 - [ (E) -phenylazo] phenyl} hydrazinidine) - 7,8-dihydronaphthalene - 1,3,6-trisulfonic acid - N-cyclohexylcyclohexylamine (1:1), this is a complex chemical. Please let me know more about its safety precautions.
This chemical may have specific chemical activity and latent risk. First, do not come into direct contact during operation. It may cause irritation to the skin, eyes and respiratory tract. If you accidentally touch it, you should immediately rinse it with plenty of water and seek medical attention if necessary.
Furthermore, the place of use must be well ventilated. Avoid inhaling its dust or volatile gas to prevent damage to the respiratory system. If operating in a confined space, be equipped with effective ventilation equipment, or wear suitable respiratory protection equipment.
Storage should be placed in a cool, dry and ventilated place. Keep away from fire and heat sources to prevent chemical reactions that can cause danger. At the same time, it should be stored separately from other chemicals to avoid interaction.
During use, be sure to follow established operating procedures and safety guidelines. If there is anything unclear, you need to consult a professional, and you must not act without authorization to avoid major disasters. This is the key to ensuring your own safety and the success of the experiment, and you should keep it in mind.