As a leading (Betar)-Beta-[[(1,1-Dimethylethoxy)Carbonyl]Amino]-4-Fluorobenzenepropanoic Acid 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 (Betar) -Beta- [[ (1,1-Dimethylethoxy) Carbonyl] Amino] -4-Fluorobenzenepropanoic Acid?
This is the question of (β)-β -[[( 1,1-dimethylethoxy) carbonyl] amino] -4-fluorophenylpropionic acid, to know its chemical structure. In this compound, the fluorophenylpropionic acid is the backbone, and the fluorine atom is selected on the benzene ring. At β-carbon, an amino group with a specific structure is connected, and above this amino group, it is modified with (1,1-dimethylethoxy) carbonyl. Its shape is like the picture, with the benzene ring as the core, the side chain is extended, and the functional groups are in their respective positions and are related to each other, forming this specific chemical structure, with unique chemical properties and reactivity. In this structure, the benzene ring gives it a certain aromaticity, fluorine atoms affect the distribution of electron clouds, and the modified amino groups attached to β-carbon also have a great influence on the overall properties, which may be used in organic synthesis, medicinal chemistry and other fields.
What are the main uses of (Betar) -Beta- [[ (1,1-Dimethylethoxy) Carbonyl] Amino] -4-Fluorobenzenepropanoic Acid?
(β -(β - [( 1,1 -dimethylethoxy) carbonyl] amino) - 4 -fluorophenylpropionic acid) This substance has a wide range of uses. In the field of medicinal chemistry, it is often used as a key intermediate to help synthesize drug molecules with specific biological activities. In the field of organic synthesis, its unique structure can provide a key framework for the construction of complex organic compounds. With the help of various functional groups it contains, it can be cleverly connected with other compounds through various chemical reactions to expand the complexity and diversity of molecular structures. At the level of scientific research and exploration, scientists have used this compound to deeply explore the mechanism of organic reactions, analyze reaction paths and product characteristics under different conditions, and contribute to the development of organic synthesis chemistry.
Looking at this compound, it is crucial to the development of medicine. For example, when developing targeted drugs for specific diseases, it can be used as a basic module, chemically modified and modified, and accurately docked to disease-related targets, which is expected to become a sharp blade for conquering diseases. In the field of organic synthesis, it is like building the cornerstone of complex buildings. With its structural characteristics, many novel and unique organic molecules are constructed, providing new opportunities for the development of materials science, fine chemicals and other industries. In scientific research, it is like the key to exploring the mysteries of chemistry, helping scientists uncover the mystery of organic reactions and promoting the continuous progress of chemistry.
What is the synthesis of (Betar) -Beta- [[ (1,1-Dimethylethoxy) Carbonyl] Amino] -4-Fluorobenzenepropanoic Acid?
To prepare (Betar) -Beta- [ (1,1-dimethylethoxy) carbonyl] amino] -4 -fluorophenylpropionic acid, the method is as follows:
First, a suitable starting material is obtained, which needs to contain benzene ring, fluorine atom and a group that can be derived into propionic acid structure. Based on fluorobenzene derivatives, a substituent that can be converted into propionic acid moiety is introduced at an appropriate position. This process may involve reactions such as nucleophilic substitution and addition.
Then, the structural part of β-aminopropionic acid needs to be constructed. The amino group can be connected to the propionic acid structure by a specific reaction, and in this step, attention should be paid to the control of the reaction check point and stereochemistry to ensure that the product configuration meets the requirements of (Betar) - Beta.
Furthermore, the [ (1,1-dimethylethoxy) carbonyl] amino] protecting group is introduced at the amino group. The introduction of this protecting group can be achieved by reacting with a suitable (1,1-dimethylethoxy) carbonylation reagent, which can protect the amino group from unnecessary influence in subsequent reactions.
After each step of the reaction, it is appropriate to obtain a pure intermediate product by suitable separation and purification means, such as column chromatography, recrystallization, etc. In this way, through multi-step reactions, carefully controlling the reaction conditions of each step, including factors such as temperature, solvent, catalyst, etc., the structure of the target product is gradually constructed, and the final product is (Betar) -Beta- [ (1,1-dimethylethoxy) carbonyl] amino] -4 -fluorophenylpropionic acid.
What are the physicochemical properties of (Betar) -Beta- [[ (1,1-Dimethylethoxy) Carbonyl] Amino] -4-Fluorobenzenepropanoic Acid?
(Beta- (1,1-dimethylethoxy) carbonylamino-4-fluorophenylpropionic acid) This substance has a variety of physical and chemical properties. Its properties may be white to off-white crystalline powder, which is similar in appearance to many organic compounds.
In terms of solubility, it may have a certain solubility in organic solvents such as dichloromethane, N, N-dimethylformamide, because its structure contains lipophilic groups, which conforms to the principle of similar miscibility. However, its solubility in water may be limited because it is not a strongly polar structure.
In terms of thermal stability, when heated to a certain temperature, groups such as (1,1-dimethylethoxy) carbonyl in the molecule may undergo reactions such as decomposition, because the group is heated and other chemical bonds such as C-O bonds may break.
In terms of chemical properties, amino groups can participate in reactions such as acylation and alkylation, and have nucleophilic properties. Carboxyl groups can undergo common reactions such as esterification and salt formation, exhibiting acidic group characteristics. Benzene rings can undergo electrophilic substitution reactions, because benzene rings have electron-rich properties, and fluorine atoms will affect their reactivity and localization effects. Overall, the physical and chemical properties of the compound are affected by the synergistic action of various groups in its structure, and may have specific application values in organic synthesis, drug research and development, etc.
(Betar) -Beta- [[ (1,1-Dimethylethoxy) Carbonyl] Amino] What is the price range of -4-Fluorobenzenepropanoic Acid in the market?
It is difficult to determine the price of (1,1-dimethylethoxy) carbonylamino-4-fluorophenylpropionic acid in the market today. This price often varies with many factors, such as the quality and quantity of materials, the supply and demand of the city, the production process, the sales area and channels, etc.
If the material is of high quality and sufficient quantity, the production scale is large, the production process is mature and efficient, and the price is slightly cheaper; if the quality is thin and the quantity is small, the production process is difficult, and the price is high. In addition, the supply and demand of the market are also the main reasons. If more is required and less is supplied, the price will be higher; if less is required and more is supplied, the price will be lower. The sales area is also related to the channel. In prosperous places, the price may be high through multiple layers of resale; in the place of origin, the price may be low.
Because there is no exact market situation information, it is difficult to determine the price range. For details, you need to consult chemical material suppliers, traders, or check the chemical product price information platform to get the latest and accurate price.