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What is the chemical structure of Sodium (6E) -5- {2- [4-Chloro-2- (Trifluoromethyl) Phenyl] Hydrazino} -6-Imino-4-Oxo-4, 6-Dihydronaphthalene-2-Sulfonate?
This compound is named sodium (6E) -5- {2- [4-chloro-2- (trifluoromethyl) phenyl] hydrazinyl} -6-imino-4-oxo-4,6-dihydronaphthalene-2-sulfonate. Its chemical structure is analyzed as follows:
The structural core of this structure is a naphthalene ring, which consists of two fused benzene rings, which are the basic skeleton of the compound. At the 4th position of the naphthalene ring, there is a carbonyl (C = O) substitution, which gives it the structural characteristics of 4-oxo generation. This carbonyl group has an important influence on the electron cloud distribution and chemical properties of the compound. At the 6 position of the naphthalene ring, there is an imino group (= NH), which makes this position assume the structure of 6-imino. The presence of imino groups can participate in a variety of chemical reactions and affect the acidity and alkalinity of compounds.
At the 5 position of the naphthalene ring, a side chain containing a hydrazine group is connected through a connecting group. Specifically, the starting part of the side chain is a hydrazine group (-NH-NH-), and one end of the hydrazine group is connected to the naphthalene ring and the other end is connected to a phenyl group. This phenyl group is replaced by a chlorine atom (Cl) at the 4th position and a trifluoromethyl (-CF) at the 2nd position. The introduction of these substituents significantly changes the electronic properties and steric resistance of the benzene ring, which in turn affects the physicochemical properties of the whole compound. The 2-position of the
naphthalene ring is connected to a sulfonate (-SO 🥰) and combines with sodium ions (Na 🥰) to form a sulfonate structure. Sulfonate has strong hydrophilicity, which makes the compound have a certain water solubility. The presence of sodium ions plays a key role in the ionic properties and stability of the compound.
Sodium (6E) -5- {2- [4-Chloro-2- (Trifluoromethyl) Phenyl] Hydrazino} -6-Imino-4-Oxo-4, what are the main uses of 6-Dihydronaphthalene-2-Sulfonate?
Sodium (6E) - 5 - {2- [4-chloro-2- (trifluoromethyl) phenyl] hydrazine} - 6-imino-4-oxo-4,6-dihydronaphthalene-2-sulfonate, which is widely used. In the field of medicine, it can be used as a key intermediate to participate in the synthesis of specific drugs through subtle reaction paths, providing help to overcome disease problems.
In the chemical industry, its unique chemical structure may serve as an efficient catalyst to significantly increase the reaction rate, optimize the reaction process, and promote more efficient and orderly chemical production. In the field of materials science, it also has its place. It can be used as a modifier to skillfully integrate into the material system to improve the properties of materials, such as enhancing the stability of materials, improving the corrosion resistance of materials, etc., and contributing to the development and optimization of new materials.
The application of this substance in different fields depends on its unique chemical properties and structural characteristics. It is like a delicate key to open the door to technological innovation and development in various fields, and plays an indispensable role in many aspects.
Sodium (6E) -5- {2- [4-Chloro-2- (Trifluoromethyl) Phenyl] Hydrazino} -6-Imino-4-Oxo-4, what are the physical properties of 6-Dihydronaphthalene-2-Sulfonate?
Sodium (6E) - 5 - {2 - [4-chloro-2 - (trifluoromethyl) phenyl] hydrazine} - 6-imino-4-oxo-4,6-dihydronaphthalene-2-sulfonate, this is an organic compound. Its physical properties are quite important, and it is related to the performance of this compound in various environments and reactions.
Looking at its morphology, it is often in a solid state, which is determined by the characteristics of intermolecular forces. Intermolecular forces, such as van der Waals forces, hydrogen bonds, etc., make molecules attract tightly and maintain solid structures.
When it comes to color, it is mostly white or off-white. The formation of this color is related to the absorption and reflection characteristics of light by molecules. The distribution of electron clouds in the molecular structure determines its absorption of light of different wavelengths, while the unabsorbed light is reflected and then shows a specific color.
Solubility is also a key property. In water, its solubility may vary, which is affected by the polarity of the molecule. The molecule of the compound contains both polar groups, such as sulfonic acid groups, which are hydrophilic, and non-polar parts, such as aromatic ring structures. The balance of polar and non-polar parts determines the degree of solubility in water. In general, the presence of sulfonic acid groups makes the compound hydrophilic to a certain extent, but non-polar parts such as aromatic rings limit its solubility, or only slightly soluble or partially soluble in water.
As for the melting point, it is also an important physical parameter. The melting point depends on the strength of the intermolecular force. The stronger the intermolecular force, the higher the energy required to make the molecule break away from the lattice structure, and the higher the melting point. This compound has a specific melting point due to specific molecular structures and interactions. This melting point can be used for identification and purity judgment. When the purity of the compound is high, the melting point range is relatively narrow; if it contains impurities, the melting point decreases and the melting range becomes wider.
Sodium (6E) -5- {2- [4-Chloro-2- (Trifluoromethyl) Phenyl] Hydrazino} -6-Imino-4-Oxo-4, What is the production method of 6-Dihydronaphthalene-2-Sulfonate?
To prepare sodium (6E) - 5 - {2 - [4 - chloro - 2 - (trifluoromethyl) phenyl] hydrazine} - 6 - imino - 4 - oxo - 4,6 - dihydronaphthalene - 2 - sulfonate, the method is as follows:
First take an appropriate amount of 4 - chloro - 2 - (trifluoromethyl) aniline, combine it with an appropriate hydrazine reagent, in a suitable reaction solvent, under the action of a catalyst, control it at an appropriate temperature and reaction time, so that it undergoes a condensation reaction to generate 2 - [4 -Chloro-2- (trifluoromethyl) phenyl] hydrazine.
Then, with a specific naphthalene derivative whose structure should contain a suitable active group, and the above-mentioned 2 - [4-chloro-2- (trifluoromethyl) phenyl] hydrazine, in another reaction system, a suitable base substance is added as a catalyst, and a nucleophilic substitution reaction is carried out under appropriate temperature conditions, and the basic framework of the target product is gradually constructed.
After the reaction is completed, the reaction mixture needs to be separated and purified. The organic phase containing the target product can be initially separated by extraction with a suitable organic solvent. After that, the product is further purified by fine separation methods such as column chromatography or recrystallization to improve its purity.
Finally, the purified product is reacted with an appropriate amount of sodium source under appropriate reaction conditions to convert the product into the corresponding sodium salt, namely sodium (6E) -5- {2- [4-chloro-2- (trifluoromethyl) phenyl] hydrazine} -6-imino-4-oxo-4,6-dihydronaphthalene-2-sulfonate. During the whole process, it is necessary to precisely control the conditions of each step of the reaction, and to test the purity and structure of the product in detail to ensure that a qualified product can be obtained.
Sodium (6E) -5- {2- [4-Chloro-2- (Trifluoromethyl) Phenyl] Hydrazino} -6-Imino-4-Oxo-4, 6-Dihydronaphthalene-2-Sulfonate What are the precautions during use?
Sodium (6E) -5- {2- [4-Chloro-2- (trifluoromethyl) phenyl] hydrazino} -6-imino-4-oxo-4, 6-dihydronaphthalene-2-sulfonate is a chemical substance. When using it, many things need to be paid attention to.
First, safety protection must be comprehensive. This chemical may be dangerous, and protective equipment is indispensable when exposed. If you wear suitable protective gloves, avoid direct contact with the skin, which can cause allergies or other health problems due to chemicals or absorption through the skin. Eye protection is also crucial, and goggles should be worn to prevent it from accidentally splashing into the eyes and causing damage to the eyes. At the same time, wear a protective mask to prevent inhalation of dust or volatile gases of the substance and avoid irritation or poisoning of the respiratory tract.
Second, the operating environment should be treated with caution. It should be operated in a well-ventilated place. If the ventilation is not good, the volatile gas of chemicals will accumulate in the air, which will not only affect the health of the operator, but also may cause safety accidents. And the operating table should be kept clean and dry to prevent other impurities from mixing with the chemical and affecting its properties and experimental results.
Third, the method of use and dosage must be accurate. Use it in strict accordance with established procedures and experimental requirements, and do not change the dosage at will. Too much or too little dosage may lead to experimental failure or unexpected consequences. When dissolving or diluting the substance, choose the correct solvent and method to ensure that it is fully dissolved and evenly dispersed to ensure the accuracy of the experimental data.
Fourth, the storage process should not be ignored. Store it in a dry, cool and ventilated place, away from fire and heat sources, because it may be flammable or easily decomposed by heat. At the same time, it should be stored separately from other chemical substances to avoid mutual reaction. Make a good mark, indicating the name, specification and date of information for future search and management.
When using Sodium (6E) -5- {2- [4-Chloro-2- (trifluoromethyl) phenyl] hydrazino} -6-imino-4-oxo-4, 6-dihydronaphthalene-2-sulfonate, all aspects must be strictly treated to ensure safety and the smooth progress of the experiment.