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

This is a compound of (8Z) -7-oxo-8- (2- {4- [ (E) -phenyldiazo] phenyl} hydrazinido) -7,8-dihydronaphthalene-1,3-disulfonic acid and N-cyclohexylcyclohexylamine (1:1).
To clarify its chemical structure, it is necessary to first look at (8Z) -7-oxo-8- (2- {4- [ (E) -phenyl diazo] phenyl} hydrazine fork) -7,8-dihydronaphthalene-1,3-disulfonic acid part. Above the naphthalene ring, there is a carbonyl group at the 7th position, the 8th position is connected to the hydrazine fork containing a specific substituted phenyl group, and the 1st and 3rd positions are connected to a sulfonic acid group. In this structure, the naphthalene ring is the basic skeleton, and the carbonyl group gives it specific reactivity, while the phenyl-substituted hydrazine fork containing diazo groups adds structural complexity and special properties.
Looking at N-cyclohexyl cyclohexylamine again, it is an amine compound containing two cyclohexyl groups. Both cyclohexyl groups are saturated alicyclic structures and are connected by nitrogen atoms.
The two combine 1:1, or form specific chemical structures through ionic bonds, hydrogen bonds, etc. Compounds with such structures may have potential applications in materials science, pharmaceutical chemistry, etc. In materials science, or because of its unique structure, it exhibits special optical and electrical properties; in pharmaceutical chemistry, or because of its special molecular shape and functional group, it can interact with specific biological targets and exhibit pharmacological activity.

(8Z) -7-oxo-8- (2- {4- [ (E) -phenylazo] phenyl} hydrazidinyl) -7,8-dihydronaphthalene-1,3-disulfonic acid-N-cyclohexylcyclohexylamine (1:1) This material has the following physical properties:
Its appearance or crystalline powder, color may vary depending on purity, high purity or white. In terms of melting point, it needs to be determined by precise experiments and is expected to be in a certain temperature range. This temperature range is crucial for its physical state transformation and affects its stability and application scenarios under different conditions.
In terms of solubility, in polar organic solvents or show a certain solubility, such as in ethanol, acetone and other solvents, according to the principle of similar compatibility, due to the polar groups in the molecular structure, it can form interactions with polar solvent molecules, which is conducive to dissolution. In non-polar solvents, such as n-hexane, solubility or poor.
Density is also an important physical property. Although the exact value needs to be accurately measured, according to its molecular composition and structural characteristics, it can be inferred that its density is within a certain range. This density value has an impact on its dispersion and sedimentation in various media. In addition, its hygroscopicity cannot be ignored. Certain groups in the molecular structure may cause them to absorb moisture under a specific humidity environment, which requires its storage and use conditions. It is necessary to control the ambient humidity to prevent moisture absorption from affecting quality and performance.

(This compound) is named (8Z) -7-oxo-8- (2- {4- [ (E) -phenyldiazo] phenyl} hydrazidinyl) -7,8-dihydronaphthalene-1,3-disulfonic acid-N-cyclohexylcyclohexylamine (1:1), which has applications in many fields.
In the field of dyes, due to its unique chemical structure, special color and stability, it can be used as a new type of dye component for dyeing fabrics, leather and other materials, resulting in bright and lasting tones, improving the quality and aesthetics of dyeing products.
In the field of materials science, it can be used to prepare functional materials by virtue of its own structural properties. It may endow materials with unique optical and electrical properties, and play a role in the R & D and manufacturing of optoelectronic devices such as organic Light Emitting Diodes and solar cells, promoting the development of new materials.
In the field of pharmaceutical research, its complex structure contains potential biological activities. After in-depth research and modification, it may become a lead compound for the development of new drugs, targeting specific disease targets, providing new options and hope for disease treatment.
In chemical analysis, it can be used as a special chemical reagent. Based on its reaction characteristics with specific substances, it can be used to detect, isolate and identify certain compounds, helping to carry out chemical analysis more accurately and efficiently.

To prepare (8Z) -7-oxo-8- (2- {4- [ (E) -phenyldiazo] phenyl} hydrazine fork) -7,8-dihydronaphthalene-1,3-disulfonic acid-N-cyclohexylcyclohexylamine (1:1), you can follow the following ancient method.
First take an appropriate amount of naphthalene derivatives, in a specific reaction vessel, and dissolve them in a suitable organic solvent. The organic solvent needs to have good solubility and stability, such as dichloromethane. Then, a precisely measured diazotization reagent is slowly added, and the reaction is carried out under the condition of low temperature and tight stirring. This low temperature environment needs to be maintained with caution, because the diazotization reaction is quite sensitive to temperature, and the reaction is easy to fail if it is not careful. During the reaction, closely observe the color change of the solution and the reaction process. When the reaction reaches the expected level, an intermediate product containing a specific diazo structure is obtained.
Transfer this intermediate product into another clean reaction instrument and add it to the reaction system containing cyclohexyl cyclohexylamine. In this system, the choice of solvent is also crucial, and alcohol solvents can be selected to promote the reaction of the two. At the same time, an appropriate amount of catalyst is added to accelerate the reaction and shorten the reaction time. When reacting, it is necessary to control the reaction temperature and duration. After careful observation and precise control, the two can fully react to achieve the expected stoichiometric ratio.
After the reaction is completed, the product is separated and purified. First, the insoluble impurities are removed by filtration, and then the insoluble impurities are extracted multiple times with a suitable organic solvent to remove the unreacted raw materials and by-products. After that, the product can be purified by distillation, crystallization, etc., to obtain pure (8Z) -7-oxo-8- (2- {4- [ (E) -phenyldiazo] phenyl} hydrazine fork) -7,8 -dihydronaphthalene-1,3 -disulfonic acid-N-cyclohexylcyclohexylamine (1:1). Every step of operation needs to be careful to ensure the purity and yield of the product.

This is related to the stability of (8Z) -7-oxo-8- (2- {4- [ (E) -phenyldiazenyl] phenyl} hydrazine fork) -7,8-dihydronaphthalene-1,3-disulfonic acid-N-cyclohexylcyclohexylamine (1:1). The stability of this compound needs to be considered from its structural characteristics and the environment.
Looking at its structure, it contains a complex naphthalene ring structure and is connected with functional groups such as sulfonic acid groups and nitrogen-nitrogen double bonds. The sulfonic acid group is hydrophilic and can enhance the stability of the compound in polar solvents; while the nitrogen-nitrogen double bond has higher chemical activity. When exposed to light, heat or specific chemical reagents, or reacts, the stability is reduced.
In terms of environmental factors, the temperature increases, the thermal movement of molecules intensifies, or the vibration of chemical bonds is enhanced, which increases the reactivity and decreases the stability; under light, especially light of specific wavelengths, or induces luminescent chemical reactions, it affects the structure of nitrogen-nitrogen double bonds and other structures and weakens the stability.
From the perspective of acid-base environment, if it is in a strong acid or strong base environment, the sulfonic acid group, amine group and other functional groups may undergo protonation or deprotonation reaction, which changes the charge distribution of the compound and the intermolecular forces, which also affects the stability.
Exists in the air, oxygen or reacts with active functional groups, such as nitrogen oxide double bonds, resulting in structural changes and impaired stability. And humidity also plays a role. High humidity environments may trigger reactions such as hydrolysis, which affect its stability.
In general, (8Z) -7-oxo-8- (2- {4- [ (E) -phenyldiazenyl] phenyl} hydrazine fork) -7,8-dihydronaphthalene-1,3-disulfonic acid-N-cyclohexylcyclohexylamine (1:1) The stability is affected by many factors of structure and environment. During practical application and storage, it is necessary to properly control the environmental conditions to ensure its stability.