As a leading Sodium 4-[(E)-{4-[Benzyl(Ethyl)Amino]Phenyl}{(4E)-4-[Benzyl(Ethyl)Iminio]Cyclohexa-2,5-Dien-1-Ylidene}Methyl]Benzene-1,3-Disulfonate supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.
What is the chemical structure of Sodium 4- [ (E) - {4- [Benzyl (Ethyl) Amino] Phenyl} { (4E) -4- [Benzyl (Ethyl) Iminio] Cyclohexa-2,5-Dien-1-Ylidene} Methyl] Benzene-1,3-Disulfonate?
This compound is named 4- [ (E) - {4- [benzyl (ethyl) amino] phenyl} { (4E) -4 - [benzyl (ethyl) imino] cyclohexyl-2,5 -diene-1 -subunit] methyl} benzene-1,3 -disulfonic acid, sodium, and its chemical structure is analyzed as follows:
The core structure of this compound is benzene-1,3 -disulfonic acid, sodium part, that is, at the 1st and 3rd positions of the benzene ring, the sulfonate is connected to the sodium ion and forms a salt. Then, a more complex substituent is connected at the 4th position of the benzene ring. This substituent is first a structure linked by a double bond, namely (E) - {4- [benzyl (ethyl) amino] phenyl} and { (4E) -4 - [benzyl (ethyl) imino] cyclohexyl-2,5-diene-1-subunit] methyl}.
wherein the { (4E) -4 - [benzyl (ethyl) imino] cyclohexyl-2,5 -diene-1 -subunit] methyl} moiety is a cyclohexadiene structure, with benzyl (ethyl) imino substituted at the 4th position, and the 1st position is connected to a methylene, which in turn is connected to the aforementioned {4- [benzyl (ethyl) amino] phenyl} by a double bond. The {4- [benzyl (ethyl) amino] phenyl} moiety is connected to the benzyl (ethyl) amino group at the 4th position of the phenyl ring. The benzyl (ethyl) amino group is a nitrogen atom that is connected to both benzyl and ethyl. Therefore, the components are combined to form the chemical structure of the complex compound.
Sodium 4- [ (E) - {4- [Benzyl (Ethyl) Amino] Phenyl} { (4E) -4- [Benzyl (Ethyl) Iminio] Cyclohexa-2,5-Dien-1-Ylidene} Methyl] What are the common uses of Benzene-1,3-Disulfonate?
Sodium + 4 - [ (E) - {4 - [Benzyl (Ethyl) Amino] Phenyl} { (4E) -4 - [Benzyl (Ethyl) Iminio] Cyclohexa - 2,5 - Dien - 1 - Ylidene} Methyl] Benzene - 1,3 - Disulfonate is a rather complex chemical substance. Its common uses can be found in many chemical research and industrial fields.
In the field of chemical synthesis, this substance may serve as a key intermediate. Due to its unique molecular structure, it can participate in a variety of organic reactions, and through carefully designed reaction paths, it can lead to the formation of compounds with specific structures and functions. For example, when building complex organic molecules with a specific electron cloud distribution and spatial configuration, they can use their own active groups to skillfully combine with other reactants to help chemists achieve the synthesis of target products.
In the field of materials science, this compound also has potential uses. Due to its structural properties, it may endow materials with special optical, electrical or mechanical properties. For example, introducing it into a specific polymer system may improve the electrical conductivity of the material, or adjust the optical absorption and emission characteristics of the material, thereby laying the foundation for the development of new optoelectronic materials.
Furthermore, in some special catalytic reactions, the substance may exhibit catalytic activity. The combination of specific atoms and functional groups in the molecule may provide a suitable reaction check point for the reaction molecule, reduce the activation energy of the reaction, thereby accelerating the reaction process, improving the reaction efficiency and selectivity, and playing an important role in the preparation of fine chemical products.
In conclusion, Sodium + 4 - [ (E) - {4 - [Benzyl (Ethyl) Amino] Phenyl} { (4E) -4 - [Benzyl (Ethyl) Iminio] Cyclohexa - 2,5 - Dien - 1 - Ylidene} Methyl] Benzene - 1,3 - Disulfonate, with its unique molecular structure, has many applications in chemical synthesis, materials science and catalytic reactions, etc., providing rich research materials and application possibilities for the development of related fields.
How safe is Sodium 4- [ (E) - {4- [Benzyl (Ethyl) Amino] Phenyl} { (4E) -4- [Benzyl (Ethyl) Iminio] Cyclohexa-2,5-Dien-1-Ylidene} Methyl] Benzene-1,3-Disulfonate?
This is a question about the safety of the compound "Sodium+4-%5B%28E%29-%7B4-%5BBenzyl%28Ethyl%29Amino%5DPhenyl%7D%7B%284E%29-4-%5BBenzyl%28Ethyl%29Iminio%5DCyclohexa-2%2C5-Dien-1-Ylidene%7DMethyl%5DBenzene-1%2C3-Disulfonate". The compound has a complex structure, and although there is no detailed ancient book corresponding to it, its properties can be analyzed according to today's chemical theory.
From the perspective of its structure, it contains sulfonic acid radical groups, which are often hydrophilic and easily soluble and dispersed in the environment. However, the imine and amine structures containing nitrogen may involve chemical reactivity. Under specific conditions, the imine structure may participate in reactions such as addition and hydrolysis. If this substance enters the biological system, such reactions may affect the normal function of biomolecules, such as interacting with key biological macromolecules such as proteins and nucleic acids, causing disorders in physiological processes.
and its sodium salt form, in water or easily dissociated into ionic state, affecting the local ionic strength. If the ionic strength changes drastically in the environment, it may disturb the osmotic pressure regulation and enzyme activity of organisms. And contain benzene ring structure, such aromatic structures have certain hydrophobicity and stability, or are difficult to be easily degraded by organisms, or have a tendency to accumulate in the environment, pass through the food chain, or cause bioaccumulation, endangering advanced organisms in the ecosystem.
Although there is no exact ancient book as evidence, according to current chemical principles and related similar studies, this substance may pose certain safety hazards. When using and discharging, it should be carefully considered to ensure ecological and life safety.
Sodium 4- [ (E) - {4- [Benzyl (Ethyl) Amino] Phenyl} { (4E) -4- [Benzyl (Ethyl) Iminio] Cyclohexa-2,5-Dien-1-Ylidene} Methyl] What are the preparation methods of Benzene-1,3-Disulfonate?
To prepare sodium (Sodium) and 4- [ (E) - {4- [benzyl (ethyl) amino] phenyl} { (4E) -4 - [benzyl (ethyl) imino] cyclohexyl-2,5 -diene-1-subunit] methyl} benzene-1,3 -disulfonate, the method is as follows:
First, the raw materials used need to be prepared. Among them, benzyl (Benzyl), ethyl (Ethyl) related reagents, and compounds containing benzene cyclohexadiene, cyclohexadiene and other structures need to be carefully selected to ensure their purity and quality, so that the reaction can proceed smoothly.
At the beginning of the reaction, the compound containing benzene-1,3-disulfonic acid group is co-placed in a suitable reaction vessel with the reactants containing benzyl, ethylamino and imino structures in an appropriate ratio. The container must be clean and dry to prevent impurities from interfering with the reaction. The material of the container should also be considered to avoid adverse reactions with the reactants and products.
The ambient temperature and pressure of the reaction have a great influence on the reaction process. When carefully controlled to maintain the temperature at a certain stable range, the pressure should also meet the reaction requirements. If the temperature is too high, the reaction may go out of control and the product will decompose; if the temperature is too low, the reaction rate will be slow and take a long time.
During the reaction process, an appropriate amount of catalyst can be added according to the actual situation. This catalyst can effectively speed up the reaction rate, shorten the reaction time, and does not affect the purity and structure of the product. However, the amount of catalyst must also be precisely controlled. Too much or too little may affect the reaction effect.
When the reaction is carried out to a certain extent, the reaction phenomenon and monitoring results can be seen to determine whether the reaction is approaching completion. At this time, appropriate separation and purification methods need to be used to obtain a pure target product. Methods such as filtration, extraction, crystallization, etc. can be selected on demand to remove unreacted raw materials, by-products and impurities.
The whole preparation process requires the experimenter's full attention and rigorous operation of each step to obtain a pure 4- [ (E) - {4- [benzyl (ethyl) amino] phenyl} { (4E) -4 - [benzyl (ethyl) imino] cyclohexene-2,5 -diene-1-subunit] methyl} benzene-1,3 -disulfonate sodium salt product.
Is Sodium 4- [ (E) - {4- [Benzyl (Ethyl) Amino] Phenyl} { (4E) -4- [Benzyl (Ethyl) Iminio] Cyclohexa-2,5-Dien-1-Ylidene} Methyl] Benzene-1,3-Disulfonate chemically reactive with other substances?
"Sodium + 4 - [ (E) - {4 - [Benzyl (Ethyl) Amino] Phenyl} { (4E) -4 - [Benzyl (Ethyl) Iminio] Cyclohexa - 2,5 - Dien - 1 - Ylidene} Methyl] Benzene - 1,3 - Disulfonate" is a rather complex chemical substance. Its structure contains phenyl ring, amine group, imine group and sulfonic acid group, which makes its chemical properties quite unique.
It is difficult to generalize whether it is easy to react chemically with other substances. In case of electrophilic reagents, due to the electron-rich region in the structure, such as the amine group of the electron conductor connected to the benzene ring, the electrophilic substitution reaction may be initiated. For example, the adjacent, para-position of the benzene ring or the positioning effect of the amine group are vulnerable to attack by electrophilic reagents.
However, in case of nucleophiles, the carbon of the imine group has a certain positive electricity, or nucleophilic addition reaction may occur. However, the difficulty of the actual reaction still needs to consider the reaction conditions, such as temperature, solvent, catalyst, etc. High temperature may accelerate the reaction rate, specific solvents may affect the solubility and reactivity of the reactants, and suitable catalysts may greatly reduce the activation energy of the reaction and promote the reaction.
Furthermore, the sulfonic acid group makes the substance water-soluble to a certain extent, which may affect the reaction system in which it participates. In the aqueous phase reaction, its solubility may be conducive to the contact and reaction of the reactants. However, in the non-aqueous phase system, its solubility is poor, or it hinders the reaction. Therefore, it is necessary to consider whether the substance is prone to chemical reactions with other substances, and it is difficult to answer simply.