As a leading (1,2-Phenylenebis(Oxy))Bis(Ethane-2,1-Diyl)Bis(4-Methylbenzenesulfonate) 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 (1,2-phenylenebis (oxy)) bis (ethane-2,1-diyl) bis (4-methylbenzenesulfonate)?
The chemical structure of (1,2-imino bis (carbonyl)) bis (acetyl-2,1-diyl) bis (4-methylbenzenesulfonate) is a rather complex type of structure in organic chemistry.
In this structure, the (1,2 -imino bis (carbonyl)) part is composed of an imino group (-NH-) with a carbonyl group (-C = O) on both sides. This structure is commonly found in many nitrogen-containing organic compounds with carbonyl groups. The nitrogen atom of the imino group has a pair of lone pair electrons, which can participate in many chemical reactions, such as nucleophilic reactions. Carbonyl is partially positively charged due to the electronegativity of carbon and oxygen, making it vulnerable to attack by nucleophilic reagents.
Bis (acetyl-2,1-diyl) moiety is the connection of two acetyl groups (- COCH <) through 2,1-diyl. Acetyl groups are common organic functional groups and have certain chemical activities. Under specific conditions, reactions such as hydrolysis and substitution can occur. This connection of 2,1-diyl groups makes the spatial position of the two acetyl groups interact with the chemical activity.
Bis (4-methylbenzenesulfonate) moiety is formed by connecting a methyl group (- CH <) to a 4-position benzene ring, and the benzene ring is connected to a sulfonate group (- SO < R). Methyl as the power supply group will affect the electron cloud density distribution of the benzene ring, causing the electron cloud density of the benzene ring to increase relatively, which in turn affects the substitution reactivity on the benzene ring; sulfonate group is a good leaving group, which is easy to leave and promote the reaction in the process of nucleophilic substitution.
Overall, the chemical structure of (1,2-imino bis (carbonyl)) bis (acetyl-2,1-diyl) bis (4-methylbenzenesulfonate), due to the interaction and synergy of various functional groups, endows the compound with unique chemical properties and reactivity, and may have potential application value in organic synthesis, medicinal chemistry and other fields.
What are the physical properties of (1,2-phenylenebis (oxy)) bis (ethane-2,1-diyl) bis (4-methylbenzenesulfonate)?
(1,2-Iminobis (carbonyl)) bis (acetyl-2,1-diyl) bis (4-methylbenzenesulfonate) This material has the following physical properties:
Looking at its shape, it is mostly white to slightly yellow crystalline powder under normal conditions. The texture is uniform and delicate. Under the illumination of light, there are occasional subtle shimmer, like hidden shimmer. Its particle size is relatively uniform, and the particle size is roughly within a specific range, but this range varies slightly due to the preparation process, or there are subtle changes.
Smell the smell, almost no obvious smell, close to the smell, only a very light smell, like the air of the free trace, difficult to describe exactly, no pungent, choking state, in the sense of smell, relatively mild.
As for solubility, in organic solvents, such as acetone, dichloromethane, etc., show good solubility. When mixed with it, with the help of moderate stirring, it can quickly and uniformly disperse, gradually fusing into one, forming a clear and transparent solution. This property may be due to the interaction between specific groups in the molecular structure and organic solvent molecules. In water, its solubility is slightly inferior. Although it is not completely insoluble, it can only reach a slight degree of solubility. Only a small amount of material is slowly diffused in water, and the solution is slightly turbid. After standing over time, some of the insoluble matter gradually sinks to the bottom.
When it comes to the melting point, it is roughly in a certain temperature range after precise determination. When it is heated up, near the lower limit of this temperature range, the substance begins to soften, like a sleeping thing gradually waking up; when the temperature rises to the range, the substance rapidly changes from solid to liquid. This melting point range is relatively narrow, indicating that its purity is quite high, its internal structure is regular and orderly, and the intermolecular forces are stable and uniform.
Looking at its density, it is slightly higher than that of common organic solvents. When you weigh the container containing this substance by hand, you can feel it is slightly heavier to the touch. This density characteristic may be closely related to the type, quantity and arrangement of atoms in the molecule, resulting in a relatively large mass of substances contained in a unit volume.
What are the main uses of (1,2-phenylenebis (oxy)) bis (ethane-2,1-diyl) bis (4-methylbenzenesulfonate)?
(1,2-Iminobis (oxy)) bis (ethyl-2,1-diol) bis (4-methylbenzenesulfonate) This compound has a wide range of main uses. In the field of medicinal chemistry, it is often used as a key intermediate in organic synthesis. Due to its special molecular structure, many bioactive compounds can be derived through various chemical reactions, which is of great help in the creation of new drugs.
It also has its uses in materials science. Or can participate in the preparation of polymer materials, through its polymerization with other monomers, endow the material with unique properties, such as improving the solubility and thermal stability of the material, or making the material have special functions, such as biodegradability, targeted identification, etc.
In the field of fine chemicals, it is also an important raw material. It can be used to synthesize fine chemicals such as special surfactants and catalyst ligands. Such fine chemicals are indispensable in the daily chemical, electronics, petrochemical and other industries, and can improve the performance and quality of products.
With its unique structure and reactivity, this compound plays a key role in many fields, and is of great significance in promoting technological progress and product innovation in related industries.
What is the synthesis method of (1,2-phenylenebis (oxy)) bis (ethane-2,1-diyl) bis (4-methylbenzenesulfonate)?
To prepare (1,2-iminobis (carbonyl)) bis (acetyl-2,1-diyl) bis (4-methylbenzenesulfonate), the method is as follows:
First take an appropriate amount of 4-methylbenzenesulfonate, put it in a suitable reactor, catalyze with a specific catalyst, and esterify with an appropriate amount of alcohol compound. Control the temperature, pressure and time of the reaction to make the reaction fully proceed to obtain 4-methylbenzenesulfonate.
Then, take another reaction vessel, mix 1,2-diamine compounds with carbonylation reagents in a certain proportion, and react under appropriate conditions to generate (1,2-imino bis (carbonyl)) derivatives. This process requires precise control of reaction conditions, such as temperature, pH, etc., to ensure the purity and yield of the product.
Then take the acetyl-2,1-diyl-related reactants and make them condensate with the (1,2-imino bis (carbonyl)) derivatives generated above. This step also requires attention to the reaction environment to avoid side reactions.
Finally, the obtained intermediate product is reacted with the prepared 4-methylbenzenesulfonate in a specific reaction system. By adjusting the reaction parameters, it is fully reacted to obtain the target product (1,2-imino bis (carbonyl)) bis (acetyl-2,1-diyl) bis (4-methylbenzenesulfonate). After the reaction is completed, the pure product can be obtained through post-processing steps such as separation and purification. The whole synthesis process requires fine operation and strict control of the reaction conditions at each step to improve the quality and yield of the product.
What are the precautions for using (1,2-phenylenebis (oxy)) bis (ethane-2,1-diyl) bis (4-methylbenzenesulfonate)?
(1,2-Iminobis (carbonyl)) bis (ethyl-2,1-diyl) bis (4-methylbenzenesulfonate) This product is extraordinary, and when using it, many matters need to be paid attention to.
Bear the brunt, this product is chemically active, in contact with others, or react. In case of strong oxidants, or severe reactions, or even dangerous. Therefore, when using, keep away from such substances to prevent accidents.
Furthermore, the operation must be cautious. Because it may be corrosive, if it accidentally touches the skin, rinse it with plenty of water and seek medical attention immediately. In the eyes, it is even more critical. Rinse immediately without delay, and then seek medical help urgently.
The method of storage should not be ignored. It should be placed in a cool, dry and ventilated place, away from fire and heat sources. Sealed and stored to avoid moisture and deterioration, or reaction with air components, which will damage its quality and efficiency.
In addition, the user should be professionally trained and familiar with the operation process and emergency measures. In the place, it is necessary to have corresponding protective equipment, such as protective clothing, gloves, goggles, etc., to ensure safety. After use, the remaining materials and waste should be properly disposed of according to regulations, and should not be discarded at will, so as not to pollute the environment.
All of these are necessary for the use of (1,2-imino bis (carbonyl)) bis (ethyl-2,1-diyl) bis (4-methylbenzenesulfonate). Those who need attention must not be slack and neglect, which will lead to disaster.