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What is the chemical structure of 4-Fluoro-Alpha- (2-Methyl-1-Oxopropyl) -Gama-Oxo-N, Beta-Diphenylbenzene Butaneamide?
This is the chemical structure analysis of 4-fluoro - α -( 2-methyl-1-oxopropyl ) - γ - oxo-N, β-diphenylbenzamide.
This compound has phenylbutylamide as its main structure. In the structure of phenylbutylamide, the γ-position has a carbonyl group, which gives the molecule specific reactivity and chemical properties. Because of its electrophilicity, it can participate in many chemical reactions. The α-position is connected with 2-methyl-1-oxopropyl, and the introduction of this substituent changes the spatial structure and electron cloud distribution of the molecule. The presence of methyl increases the steric hindrance, and the carbonyl of 1-oxopropyl also has a significant impact on the overall properties of the molecule.
Furthermore, the 4-position on the benzene ring has fluorine atom substitution. The fluorine atom has strong electronegativity, and its presence significantly affects the electron cloud density of the benzene ring, which in turn changes the physical and chemical properties of the molecule, such as enhancing the polarity of the molecule, affecting its solubility and reactivity. The conjugation system of N and β-positions is connected with phenyl, and the phenyl group increases the degree of electron delocalization of the molecule, which affects the stability and spectral properties of the molecule The presence of multiple benzene rings also makes the molecule more rigid and planar, which has an important impact on molecular interactions such as π-π stacking, which may be reflected in crystal structure and biological activity.
In summary, the chemical structure of this compound is composed of the main chain of phenylbutylamide and multiple different substituents, and the interaction of each part determines its unique chemical and physical properties.
4-Fluoro-Alpha- (2-Methyl-1-Oxopropyl) -Gama-Oxy-N, Beta-Diphenylbenzene What is the main use of Butaneamide
4-Fluoro - α -( 2-methyl-1-oxopropyl ) - γ - oxo-N, β-diphenylphenylbutylamide, this is an organic compound. Looking at its name, it can be seen that its structure is complex and it is composed of many specific groups.
In the field of medicine, such complex organic compounds may have unique biological activities or can be used as potential drug lead compounds. Its special structure may interact with specific targets in organisms, such as matching with the activity check point of certain enzymes, thereby regulating the activity of enzymes and participating in the regulation of disease-related physiological processes. It may also bind to cell surface receptors, affect cell signaling pathways, and be helpful in the treatment of specific diseases.
In the field of organic synthesis, this compound can act as a key intermediate. With its diverse functional groups in its structure, it can further derive more structurally rich compounds through a series of organic reactions, such as nucleophilic substitution, addition reactions, etc., providing an important material basis for the research and development of organic synthetic chemistry, helping scientists explore new organic molecular architectures and expand the variety and application scope of organic compounds.
What are the physical properties of 4-Fluoro-Alpha- (2-Methyl-1-Oxopropyl) -Gama-Oxo-N, Beta-Diphenylbenzene Butaneamide
4-Fluorine - α -( 2-methyl-1-oxopropyl ) - γ - oxo-N, β-diphenylphenylbutylamide, this is an organic compound. It has several physical properties, let me tell you one by one.
First, the appearance, under normal temperature and pressure, is mostly white to white crystalline powder, just like winter snow, delicate and pure. The melting point of this compound is about 145-148 ° C. When the temperature gradually rises to the melting point, it is like melting ice and snow, its solid state slowly turns into a liquid state, and the intermolecular forces change at this temperature.
Furthermore, when it comes to solubility, it has good solubility in organic solvents such as dichloromethane, chloroform, N, N-dimethylformamide. The reason for this phenomenon is that the molecular structure of the compound can form interactions such as van der Waals force and hydrogen bond between these organic solvent molecules, so it is easy to dissolve in it. However, the solubility in water is very small, because water is a highly polar solvent, which does not match the intermolecular forces of the compound. It is like a square chisel and is difficult to be compatible.
Because its molecules contain many conjugated structures, it has a certain stability. However, under extreme conditions such as strong acids, strong bases or high temperatures, the structure may change. For example, in the case of strong acids, some chemical bonds in the molecule may be attacked by protonation, causing structural rearrangement; in the case of strong bases, some functional groups may undergo hydrolysis reactions, changing their original chemical composition and structure.
In addition, its density is also one of the important physical properties. Although the specific value is not detailed, it can be slightly inferred from its molecular structure and relative molecular mass. Due to the structure of fluorine atoms and benzene rings in the molecule, the relative molecular mass is large and the structure is relatively compact, so it is inferred that its density is slightly higher than that of ordinary organic compounds.
In summary, the physical properties of 4-fluoro - α -( 2-methyl-1-oxopropyl ) - γ - oxo-N, β-diphenylbenzamide are closely related to its molecular structure, which is an important guide for its application in organic synthesis, drug development and other fields.
4-Fluoro-Alpha- (2-Methyl-1-Oxopropyl) -Gama-Oxy-N, Beta-Diphenylbenzene Butaneamide
The preparation method of 4-fluoro - α -( 2-methyl-1-oxopropyl ) - γ - oxo-N, β-diphenylphenylbutylamide is like the ancient alchemy, which requires a delicate method and a rigorous order.
At the beginning, take an appropriate amount of fluorobenzene derivatives as the base material, which is the foundation of building molecules. It needs to be finely purified to ensure purity and flawlessness before proceeding to the next step of the reaction.
Then, the related reagent of 2-methyl-1-oxopropyl is slowly added to the fluorobenzene derivative in a precise amount. During the reaction, temperature control is very critical, and it needs to be maintained in a specific temperature range, just like the control of the temperature during alchemy, which cannot be exceeded or inferior. At this temperature, the two chemically react and blend with each other, forming a prototype.
In addition, a reagent for constructing the γ-oxo structure is added, and this reagent reacts with the previous reactants again delicately. At this time, a specific catalyst may be added to help the reaction proceed smoothly, just like adding a special medicine during alchemy to catalyze the change. In this process, pay close attention to the progress of the reaction, adjust the reaction conditions in a timely manner, such as pressure, reaction time, etc., to ensure the formation of the required intermediate products.
When the intermediate product is obtained, a diphenyl-containing reagent is introduced to react with the intermediate product in a suitable solvent. The choice of this solvent is a matter of success or failure, and it needs to have good compatibility with the reactants. During the reaction, careful operation is used to make the parts precisely combine, and finally 4-fluoro - α -( 2-methyl-1-oxopropyl ) - γ - oxo-N, β-diphenylbenzamide.
The reaction is over, and the product still needs to go through the process of separation and purification. Distillation, extraction, recrystallization and other methods are used to remove impurities and obtain a pure target product. Every step needs to be careful, such as the ancient alchemy method.
4-Fluoro-Alpha- (2-Methyl-1-Oxopropyl) -Gama-Oxo-N, Beta-Diphenylbenzene Butaneamide What are the precautions during use
4-Fluoro-alpha - (2-methyl-1-oxopropyl) -gamma-oxo-N, beta-diphenylphenylbutylamide, this is a complex organic compound. During use, many matters need to be paid careful attention.
Bear the brunt, safety protection is of paramount importance. Due to its chemical nature or potential danger, it is necessary to wear appropriate protective equipment when contacting, such as gloves, goggles and protective clothing, to prevent the substance from coming into direct contact with the skin and eyes, and to avoid inhaling its dust or vapor to prevent damage to the respiratory tract.
Furthermore, precise control of the dosage is indispensable. This compound may have high activity, and the dosage deviation or reaction results are very different. Therefore, it is necessary to strictly control the dosage with precise measuring tools according to the reaction requirements and relevant standards to ensure that the reaction proceeds as expected.
In addition, the fine regulation of reaction conditions cannot be ignored. Factors such as temperature, pH, and reaction time have a great impact on the reaction process and product purity. For example, a specific temperature range can promote the efficient occurrence of the reaction. Too high or too low temperature may cause abnormal reaction rates or the formation of by-products. Therefore, the reaction conditions need to be precisely regulated with the help of temperature control equipment and pH regulators.
Storage is also exquisite. It should be stored in a dry, cool and well-ventilated place, away from fire, heat and oxidants to prevent deterioration or dangerous reactions. At the same time, the storage container must be well sealed to avoid contact with air, moisture, etc.
Finally, proper disposal after use should not be underestimated. Its waste or residue needs to be disposed of in accordance with relevant regulations and environmental protection requirements, and must not be discarded at will to avoid pollution to the environment. In short, when using this compound, all aspects need to be paid attention to in order to ensure safe operation and achieve the desired effect.