As a leading 3-Amino-2,4,6-Triiodohydrocinnamic 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 3-amino-2,4, 6-triiodohydrocinnamic Acid?
3 - amino - 2,4,6 - triiodohydrocinnamic Acid is 3 - amino - 2,4,6 - triiodophenylpropionic acid, and its chemical structure is as follows.
The main structure of this compound is phenylpropionic acid. The phenylpropionic acid is a structure formed by connecting the benzene ring with propionic acid. On the benzene ring, there are iodine atoms at the 2,4,6 positions respectively. The introduction of this iodine atom greatly changes the electron cloud density and spatial structure of the benzene ring. On the α-carbon of propionic acid, there is an amino group connected. This amino group is basic and can react with acids to form corresponding salts. At the same time, the presence of the benzene ring endows this compound with certain aromaticity, which affects its physical and chemical properties. Because of its large atomic radius and high electronegativity, iodine atoms have a great influence on the physical properties of molecules such as polarity, boiling point and melting point, and also affect the activity and selectivity of the compound to participate in chemical reactions. Overall, the interaction of various groups in the chemical structure of 3-amino-2,4,6-triiodophenylpropionic acid jointly determines its unique chemical properties and potential applications.
What are the main uses of 3-amino-2,4, 6-triiodohydrocinnamic Acid
3-Amino-2,4,6-triiodohydrocinnamic acid has a wide range of uses. It plays an important role in the field of medicine. Because of its unique structure, good biological activity and pharmacological properties, it is often a key raw material for drug research and development. It is particularly important in the preparation of contrast agents. Because it contains iodine atoms, iodine has a high atomic number, which can effectively absorb X-rays, making contrast imaging clearer, helping doctors to accurately understand the condition of organs and tissues in the body, and providing a solid basis for the diagnosis of diseases.
In addition, it also plays an important role in the field of organic synthesis. It can be used as a key intermediate to derive many organic compounds with complex structures and specific functions through various chemical reactions. This plays an indispensable role in the research and development of new materials and the preparation of fine chemicals. Chemists can skillfully design reaction paths according to their characteristics, synthesize compounds that meet different needs, and promote progress and development in related fields.
In some research fields, due to their special chemical properties, they can be used to explore specific biological processes or chemical reaction mechanisms. Scientists can use them to participate in experiments, observe and analyze reaction phenomena and results, and then deeply understand related mechanisms, open up new paths for scientific research, and help accumulate and innovate knowledge.
What are the physical properties of 3-amino-2,4, 6-triiodohydrocinnamic Acid?
3-Amino-2,4,6-triiodohydride cinnamic acid, its physical properties are also quite important, and in detail, this substance often exhibits specific properties.
Its appearance is mostly white to off-white crystalline powder, which is easy to observe and handle. In terms of solubility, it has different manifestations in specific solvents. In water, its solubility is low, but in organic solvents such as ethanol and dichloromethane, the solubility is relatively high. This property is related to the groups contained in the molecular structure. The presence of amino, carboxyl and iodine atoms affects the interaction between them and different solvent molecules.
Its melting point is also one of the key physical properties, about a certain temperature range, which is crucial for the identification and purification of the substance. When heated to the melting point, the substance changes from a solid to a liquid state. The exact temperature range of this process can be used as the basis for judging its purity.
In addition, the density of the substance also has its specific value. Although it is not a daily frequent consideration, in some situations involving accurate measurement and reaction system construction, density data is indispensable.
Furthermore, its stability is acceptable under normal conditions, but it may change when exposed to high temperature, strong light or a specific chemical environment. If exposed to strong light for a long time, it may cause changes in the molecular structure, affecting its chemical activity and related properties.
In summary, the physical properties of 3-amino-2,4,6-triiodohydrogenated cinnamic acid, such as appearance, solubility, melting point, density, and stability, play a crucial role in its applications in chemistry, medicine, and other fields.
What are the synthesis methods of 3-amino-2,4, 6-triiodohydrocinnamic Acid
The synthesis method of 3-amino-2,4,6-triiodohydrogenated cinnamic acid has been explored by many parties throughout the ages, and each has its own method.
First, cinnamic acid is used as the starting material. First, cinnamic acid and iodine are reacted under specific conditions, so that iodine atoms are introduced at specific positions on the benzene ring. This process requires careful control of the reaction temperature, time and ratio of reactants. The choice of iodine source is very critical. Common elements such as iodine, combined with suitable catalyst and solvent system, can precisely add iodine atoms to the 2,4,6-position. Subsequently, the obtained iodine-containing cinnamic acid derivatives are reduced, and the carbon-carbon double bond is reduced to a single bond, and then the hydrogenated cinnamic acid derivative is obtained. This reduction step can be selected from a suitable reducing agent, such as sodium borohydride, etc., to optimize the dosage and reaction environment according to the characteristics of the reaction substrate and reaction conditions. Finally, the carboxyl ortho-position of the hydrogenated cinnamic acid derivative is aminated. It can be achieved by various ways, such as by introducing the amino group through a substitution reaction with the help of a specific amination reagent to obtain 3-amino-2,4,6-triiodohydride cinnamic acid.
Second, phenylalanine is also used as the starting material. First, the phenylalanine is modified with a protective group to ensure the selectivity of the reaction. After that, the phenyl ring is iodized with an iodine reagent, and three iodine atoms are introduced. The activity and selectivity of the iodine substitutes need to be carefully controlled to prevent side reactions. After the iodine generation is completed, the protective group is removed to restore the original activity check point of phenylalanine. Then through a specific chemical reaction, the molecular structure is adjusted to convert it into 3-amino-2,4,6-triiodohydrogenated cinnamic acid. This synthesis route requires strict selection of reaction conditions and protective groups. It is necessary to comprehensively consider the interaction between each step of the reaction and carefully optimize the reaction parameters to improve the yield and purity of the product.
What is the price range of 3-amino-2,4, 6-triiodohydrocinnamic Acid in the market?
3-Amino-2,4,6-triiodohydrogenated cinnamic acid, this product is in the market, and its price is difficult to determine. The price often varies due to various reasons, such as differences in production, quality, and supply.
The production is different, and the price varies. If it is produced in a place with skilled skills and sufficient materials, the cost of its production may be slightly reduced, and the price may be easier; however, if the place of origin is remote and transportation is difficult, the price will increase.
The quality of the product has a great impact on the price. Those who are of high quality have very little clutter, pure and good sex, and are suitable for all kinds of things, and their price will be high; if they are of poor quality and clutter, and cannot be used, the price will be low.
The state of demand and supply is also the reason. If people are competing for it at times, and the supply is small, the so-called "what is rare is expensive", its price will rise; if the supply exceeds demand, the market is full, and merchants want to sell it quickly, the price will tend to drop.
According to the current market conditions, the price per gram may range from tens of gold to hundreds of gold. However, this is only an approximate number. The actual price still needs to be carefully observed in the current market situation and consulted with the giants of the merchants before it can be confirmed.