As a leading 4-Fluoro-Α-[2-Methyl-1-Oxopropyl]-Γ-Oxo-N,Β-Diphenylbenzene Butane Amideisobutyrylacetic Acid Methyl Ester supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.
4-Fluoro-α [2-Methyl-1-Oxopropyl] -γ-Oxo-N, β-Diphenylbenzene Butane Amideisobutyrylacetic Acid Methyl Ester
The full Chinese name of this compound is 4-fluoro - α - [ 2-methyl-1-oxopropyl ] - γ - oxo-N, β-diphenylphenylbutylamide isobutyryl acetate methyl ester. Its chemical structure is as follows:
Looking at its name, it can be seen that this compound has a complex structure and is spliced from multiple parts.
"4-fluoro - α - [ 2-methyl-1-oxopropyl ] - γ - oxo-N, β-diphenylphenylbutylamide" This part uses phenylbutylamide as the main frame. The 4 position on the benzene ring is connected to the fluorine atom, the α position is connected to 2-methyl-1-oxopropyl, and the γ position is oxo. The N atom and the β position are connected to the phenyl group respectively.
"Methyl isobutyryl acetate" is partially connected to the methyl isobutyl acetate on the basis of the above main structure. Methyl isobutyryl acetate is based on methyl acetate, in which a hydrogen atom is replaced by an isobutyryl group. Overall, this compound is composed of a phenylbutylamide-derived structure and a methyl isobutyl acetate structure through a specific connection method, and its complex structure gives it unique chemical properties and potential applications.
4-Fluoro-α [2-Methyl-1-Oxopropyl] -γ-Oxo-N, β-Diphenylbenzene Butane Amideisobutyrylacetic Acid What is the main use of Methyl Ester
4-Fluoro - α - [ 2-methyl-1-oxopropyl ] - γ - oxo-N, β-diphenylphenylbutanamide isobutyryl acetate methyl ester, this substance is used in the pharmacology of Dan formula, and has many unique uses.
View its properties, or can be used to reconcile qi and blood, dredge meridians. In the ancient alchemy, qi and blood are smooth, meridians Tongli is the key to health and beauty, and physical fitness. It may borrow its own properties to promote qi and blood operation, fill the body with qi and blood, and moisturize the skin of the viscera.
In the conditioning of the viscera, it is also beneficial. It can help the coordination of the functions of the viscera and organs, such as helping the spleen and stomach to transport and transform, so that the essence of water and valley can be better transported; it benefits the liver and kidney, nourishes the essence and fills the marrow, strengthens the tendons and strengthens the bones.
And in the disease of sores, swelling and poison, it may play a detoxifying and swelling-reducing effect. With its characteristics, it can dissolve poison and evil, dissipate swelling and knots, and restore the smoothness of the skin.
Use it with caution. Although the medicine is beneficial, it is too much. It is necessary to follow the ancient method, observe the disease in detail, measure the person's virtual and real situation, accurately match the compatibility, and control the dosage. Only then can you obtain its benefits and avoid its harm.
4-Fluoro-α [2-Methyl-1-Oxopropyl] -γ-Oxo-N, β-Diphenylbenzene Butane Amideisobutyrylacetic Acid Methyl Ester
The synthesis of 4-fluoro - α - [ 2-methyl-1-oxopropyl ] - γ - oxo-N, β-diphenylphenylbutylbenzamide isobutyryl acetate methyl ester is complicated and multi-path.
First, starting with benzene derivatives, through halogenation reaction, fluorine atoms are introduced at specific positions in the benzene ring to precisely construct the fluorobenzene structure. After the acylation reagent with a specific substituent, under suitable catalyst and reaction conditions, the acylation reaction is carried out. In this process, the reaction temperature, time and material ratio must be carefully controlled to ensure that the acyl group is successfully connected to the benzene ring, and the key intermediate is obtained.
Second, the compound containing methyl isobutyryl acetate fragments can be prepared. It can be esterified by isobutyric acid and suitable esterification reagents to form methyl isobutyrate; then it can be condensed with acetic acid derivatives under the action of strong bases and other reagents to obtain methyl isobutyl acetate related intermediates.
Third, the above two types of key intermediates are condensed in the presence of a condensing agent to construct the main structure of the target molecule. This step requires careful selection of the condensing agent, consideration of the reaction solvent and pH, in order to improve the reaction yield and selectivity.
Fourth, after the reaction is completed, the product needs to be separated and purified. Column chromatography and recrystallization are commonly used to obtain pure 4-fluoro - α - [ 2-methyl-1-oxopropyl ] - γ - oxo-N, β-diphenylphenylbutylbenzamide isobutyryl acetate methyl ester by removing impurities such as unreacted raw materials and by-products.
Each step of the reaction needs to follow the chemical principle and operating procedures, and carefully control the reaction conditions to make the synthesis process smooth and achieve the expected target product.
What are the physicochemical properties of 4-Fluoro-α [2-Methyl-1-Oxopropyl] -γ-Oxo-N, β-Diphenylbenzene Butane Amideisobutyrylacetic Acid Methyl Ester
4-Fluorine - α - [ 2-methyl-1-oxopropyl ] - γ - oxo-N, β-diphenylphenylbutanamide isobutyryl acetate methyl ester, which is a rather complex organic compound. Its physicochemical properties are crucial for its application in many fields.
In terms of physical properties, under normal temperature and pressure, this substance may appear in a solid state. Looking at its molecular structure, it contains many aromatic rings and functional groups, resulting in strong intermolecular forces, so the melting point may be relatively high. In view of the existence of polar functional groups in the molecule, such as carbonyl groups, in some polar solvents, such as ethanol and acetone, it should have a certain solubility. However, the large volume of the molecule and the hydrophobicity of the aromatic ring will limit its solubility in water, or only slightly soluble in water.
As for chemical properties, because of the carbonyl group in its structure, this is an extremely active functional group, prone to nucleophilic addition reactions such as nucleophilic addition reactions. For example, under the catalysis of acids or bases with alcohols, ester exchange reactions may occur to form new ester compounds. Amide groups also have certain reactivity, and under certain conditions, they may be hydrolyzed to form corresponding acids and amines. Furthermore, the aromatic ring part can undergo aromatic electrophilic substitution reactions, such as halogenation, nitrification, etc., thereby introducing more functional groups and expanding the possibility of its chemical derivation. In addition, the hydrogen on the α-carbon is affected by the adjacent carbonyl groups, which has a certain acidity. Under the action of strong bases, deprotonation may occur, which in turn triggers subsequent nucleophilic reactions.
4-Fluoro-α [2-Methyl-1-Oxopropyl] -γ-Oxo-N, β-Diphenylbenzene Butane Amideisobutyrylacetic Acid Methyl Ester in the market prospects
Guanfu 4 - Fluoro - α - [ 2 - Methyl - 1 - Oxo propyl ] - γ - Oxo - N, β - Diphenylbenzene Butane Amide and isobutyrylacetic Acid Methyl Ester, in the prospects of the city, it needs to be carefully observed.
4 - Fluoro - α - [ 2 - Methyl - 1 - Oxo propyl ] - γ - Oxo - N, β - Diphenylbenzene Butane Amide, unique structure, which is in the field of organic synthesis, or has potential use. However, the acceptance of the market still depends on multiple reasons. The first one is the difficulty of its preparation. If the preparation method is cumbersome and expensive, the road to promotion will be bumpy. And its performance in practical applications, whether it can emerge is also the key. If it can show excellent results in specific reactions or products, it may attract the attention of many industry players, and then expand its market.
As an ester compound, isobutyrylacetic Acid Methyl Ester has its place in the fragrance, pharmaceutical intermediates and other industries. Its prospects are also affected by fluctuations in market demand. Nowadays, the fragrance industry seeks innovation and diversity. If it can contribute its unique fragrance in new fragrance formulations, it will surely be able to occupy a seat in the market. In the field of pharmaceutical intermediates, if it can meet the needs of emerging drug research and development and participate in the synthesis of key pharmaceutical ingredients, its market prospect should be broad.
However, the two are in the market, and they are also facing the pressure of competition. If congeneric products are already preconceived and occupy the market share, the two must stand out. Or better performance, or cheaper cost, in order to have the opportunity to win. Therefore, although the prospects of the two in the market have potential, they are also full of thorns. Only by adapting to changes in the market and continuously improving, can they be expected to bloom.