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What is the chemical structure of Sodium 2- [ (E) - (3-Bromo-4-Hydroxy-5-Methylphenyl) (3-Bromo-5-Methyl-4-Oxocyclohexa-2, 5-Dien-1-Ylidene) Methyl] Benzenesulfonate?
This is a rather complex organic compound. Its name is "2 - [ (E) - (3-bromo-4-hydroxy-5-methylphenyl) (3-bromo-5-methyl-4-oxocyclohexyl-2,5-diene-1-subunit) methyl] sodium benzenesulfonate".
Looking at its naming, its structure can be gradually analyzed. "Sodium benzenesulfonate" indicates that the main structure of the compound contains a benzene ring, and the benzene ring is connected with a sulfonic acid group and forms a sodium salt form. " 2 - [ (E) - (3-bromo-4-hydroxy-5-methylphenyl) (3-bromo-5-methyl-4-oxycyclohexyl-2,5-diene-1-subunit) methyl] "This part explains that in the sodium benzenesulfonate structure, the 2-position of the benzene ring is connected to a specific structure.
Where, (E) represents the configuration and is the trans configuration." ( 3-Bromo-4-hydroxy-5-methylphenyl) "indicates the presence of a phenyl ring substituent with a bromine atom at 3, a hydroxyl group at 4, and a methyl group at 5." (3-bromo-5-methyl-4-oxycyclohexyl-2,5-diene-1-subunit) methyl "is another part of the structure, containing a hexamembered ring with a bromine atom at 3, a methyl group at 5, and a carbonyl group at 4, and this hexamembered ring is connected to a methylene group, which is eventually connected to the previously mentioned benzene ring at 2.
In summary, the structure of this compound is composed of sodium benzenesulfonate, which is connected to a complex structure of specific configurations and substituents. Its structure is quite delicate and complex, highlighting the wonders of organic chemistry.
What are the main uses of Sodium 2- [ (E) - (3-Bromo-4-Hydroxy-5-Methylphenyl) (3-Bromo-5-Methyl-4-Oxocyclohexa-2, 5-Dien-1-Ylidene) Methyl] Benzenesulfonate?
Sodium-2- [ (E) - (3-bromo-4-hydroxy-5-methylphenyl) (3-bromo-5-methyl-4-oxocyclohexyl-2,5-diene-1-subunit) methyl] benzenesulfonate is quite versatile. In the field of medicine, it can be used as an active pharmaceutical ingredient, or it can be used as a pharmaceutical agent to treat specific diseases through exquisite pharmaceutical techniques. Its unique molecular structure may specifically combine with biomolecules in the body to intervene in pathological processes and achieve therapeutic effects.
In the field of chemical research, it can be used as a key reagent. Chemists can use it to participate in various organic reactions, explore reaction mechanisms, expand organic synthesis paths, and pave the way for the creation of novel compounds.
In the field of materials science, it may have potential applications. By compounding with other materials, it may improve material properties, such as enhancing material stability, changing optical properties, etc., to meet the needs of materials in different scenarios. From this point of view, sodium-2 - [ (E) - (3-bromo-4-hydroxy-5-methylphenyl) (3-bromo-5-methyl-4-oxocyclohexyl-2,5-diene-1-subunit) methyl] benzenesulfonate has been used in many fields, which is of great significance for promoting the development of related disciplines and technological progress.
What is the synthesis method of Sodium 2- [ (E) - (3-Bromo-4-Hydroxy-5-Methylphenyl) (3-Bromo-5-Methyl-4-Oxocyclohexa-2, 5-Dien-1-Ylidene) Methyl] Benzenesulfonate?
To prepare Sodium + 2 - [ (E) - (3-bromo-4-hydroxy-5-methylphenyl) (3-bromo-5-methyl-4-oxocyclohexyl-2,5-diene-1-subunit) methyl] benzene sulfonate, the synthesis method requires multiple and delicate steps.
At the beginning, when a suitable raw material is used as the base, such as a phenyl ring compound containing the corresponding substituent is selected. The benzene ring is first brominated by a suitable brominating reagent, such as liquid bromine with a suitable catalyst, such as iron powder. The benzene ring is introduced into the bromine atom at a specific position to conform to the substitution mode required by the target product.
Then, another part of the benzene ring is modified to introduce hydroxyl, methyl and other groups. The introduction of hydroxyl groups can be achieved by a specific reaction of phenolic compounds, following the principle of organic chemistry, through nucleophilic substitution and other reaction pathways. For the addition of methyl groups, methylating reagents, such as iodomethane and a base, can be used to successfully connect the benzene ring to the methyl group under appropriate reaction conditions. After
, the cyclohexadiene structure containing carbonyl groups is constructed. By means of specific organic synthesis reactions, such as Diels-Alder reaction, suitable dienes and dienophiles can interact to form a cyclohexadiene skeleton, and then carbonyl is introduced through oxidation and other steps.
Finally, the above parts are cleverly connected to form a key carbon-carbon double bond structure to achieve [ (E) - (3-bromo-4-hydroxy-5-methylphenyl) (3-bromo-5-methyl-4-oxycyclohexyl-2,5-diene-1-subunit) methyl] part, and then react with benzenesulfonate to add sodium ions to obtain the final target product. The whole process requires fine control of the reaction conditions, such as temperature, reaction time, reagent dosage, etc., all of which are critical to success or failure. Only in this way can a pure and considerable yield of Sodium + 2- [ (E) - (3-bromo-4-hydroxy-5-methylphenyl) (3-bromo-5-methyl-4-oxycyclohexene-2,5-diene-1-subunit) methyl] benzene sulfonate be obtained.
What are the physicochemical properties of Sodium 2- [ (E) - (3-Bromo-4-Hydroxy-5-Methylphenyl) (3-Bromo-5-Methyl-4-Oxocyclohexa-2, 5-Dien-1-Ylidene) Methyl] Benzenesulfonate?
This substance is named 2- [ (E) - (3-bromo-4-hydroxy-5-methylphenyl) (3-bromo-5-methyl-4-oxocyclohexyl-2,5-diene-1-subunit) methyl] sodium benzenesulfonate, and its physical and chemical properties are as follows:
In terms of appearance, it is often in a solid state, but the specific color varies depending on the purity and preparation method, or it is a white to off-white powder, or it is crystalline.
Its solubility is quite important, and it is soluble in water. This property makes it easy to disperse and dissolve in aqueous systems, which is the foundation for its application in many fields. For example, in some chemical reactions, when water is used as a solvent, it can be used as a reactant or auxiliary agent, and its water solubility can effectively participate in the reaction.
When it comes to melting point, the exact value varies depending on the analytical method and purity, and there is roughly a specific melting point range. Measuring the melting point can be a method for determining the purity. If there are few impurities, the melting point range is narrow and approaches the theoretical value; if there are many impurities, the melting point will decrease and the range will become wider.
Stability is related to its preservation and application. Under normal conditions, if it is protected from light, hot topic and humidity, it is relatively stable. In case of strong acid, strong alkali, or high temperature and strong oxidation environment, the structure may change and the properties will change. In case of strong acid, sodium sulfonate group or reaction, the molecular structure and properties will be changed.
In terms of spectral properties, it has a characteristic absorption peak in the infrared spectrum, corresponding to different chemical bond vibrations, which is helpful for structure identification. In the ultraviolet-visible spectrum, due to the conjugate structure of the molecule, it has a specific absorption peak, which can be used for content determination and qualitative analysis.
The physical and chemical properties of this substance are of great significance for its preparation, storage, analysis and application in chemical industry, medicine and other fields. Researchers and users must know it in detail before they can make good use of it.
What is the approximate market price of Sodium 2- [ (E) - (3-Bromo-4-Hydroxy-5-Methylphenyl) (3-Bromo-5-Methyl-4-Oxocyclohexa-2, 5-Dien-1-Ylidene) Methyl] Benzenesulfonate?
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