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What are the main uses of 3-aminopyrazine-2-carboxylate?
3-Aminobutyric acid-2-hydroxyglutaric anhydride is an organic compound. Its main uses are quite extensive and it plays an important role in many fields.
In the field of medicine, this compound has potential medicinal value. It may help the research and treatment of nervous system-related diseases. Because 3-aminobutyric acid has a regulatory effect on the nervous system, or can stabilize the membrane potential of nerve cells, regulate the release and activity of neurotransmitters. The structure of 2-hydroxyglutaric anhydride may provide a new opportunity for drug development. It can be chemically modified and other means to develop drugs with specific pharmacological activities, or used to treat epilepsy, anxiety and other neurological diseases. < Br >
In the chemical industry, it can be used as a key intermediate in organic synthesis. With its unique chemical structure and active groups, it can participate in many chemical reactions and synthesize complex organic compounds. For example, by reacting with other compounds containing specific functional groups, esterification, amidation and other reactions, new polymer materials, functional additives, etc. are prepared to improve the properties of materials, such as improving the solubility and stability of materials.
In the biological field, it may participate in the metabolic process of organisms. Although the specific metabolic pathways and mechanisms still need to be further studied, the existence of such compounds may have a certain impact on basic physiological processes such as substance metabolism and energy conversion in organisms, and may be of great significance for revealing complex physiological mechanisms in organisms.
What are the physical properties of 3-aminopyrazine-2-carboxylate?
3-Hydroxybutyric acid-2-butyrolactone is also an organic compound. Its physical properties are unique and detailed as follows:
Under normal temperature and pressure, 3-hydroxybutyric acid-2-butyrolactone is often colorless to light yellow transparent liquid, pure in texture, without visible impurities, showing a flowing state, just like smart water, but with its own characteristics. This state makes it easy to mix and operate in many chemical reactions and industrial applications, and can easily participate in various reaction systems, providing a convenient basis for subsequent chemical transformations.
As for the melting point, its value is about -45 ° C. This lower melting point indicates that the substance can still maintain a liquid state in a relatively low temperature environment, which is of great significance in some processes with specific temperature requirements. For example, in some reactions that require low temperature conditions, 3-hydroxybutyric acid-2-butyrolactone can continue to act as a reaction medium or reactant in a low temperature environment due to its low melting point, ensuring the smooth progress of the reaction.
In terms of boiling point, it is about 204 ° C. A higher boiling point means that it has good thermal stability, is not easy to evaporate at higher temperatures, and can maintain its own physical state stability within a certain temperature range. This makes it not quickly vaporize and escape the reaction system due to temperature increase in some reaction processes that require heating, thus ensuring that the reaction can proceed according to the preset path and maintain the continuity and stability of the reaction.
Speaking of density, it is about 1.12g/cm ³. This density value is slightly larger than that of water, so that when it is mixed with substances with different densities such as water, it will produce stratification and other phenomena according to density differences. This can be used as an important basis in operations such as separation and purification, providing a physical method for obtaining high-purity 3-hydroxybutyric acid-2-butyrolactone.
Solubility is also one of its important physical properties. 3-Hydroxybutyric acid-2-butyrolactone is soluble in a variety of organic solvents, such as ethanol, ether, etc. This good solubility has opened a broad door for it to be used in the field of organic synthesis. In organic reactions, it is often necessary to use organic solvents to dissolve reactants to promote molecular contact and reaction. 3-Hydroxybutyric acid-2-butyrolactone can be miscible with a variety of organic solvents, which means that it can play a role in a variety of reaction systems, greatly expanding its application range.
Is the chemical property of 3-aminopyrazine-2-carboxylate stable?
The chemical properties of 3-aminoindole-2-carboxylic anhydride are quite stable under normal conditions. In this compound, the amino group interacts with the indole ring and the carboxylic anhydride structure, giving it unique stability.
The amino group has certain electron-giving properties, which can affect the electron cloud distribution of the indole ring through the conjugation effect, making the indole ring system more stable. Although the carboxylic anhydride structure has certain reactivity, in this compound, its reactivity is also limited due to the electronic and spatial effects of the surrounding groups.
3-Aminoindole-2-carboxylic anhydride rarely reacts spontaneously when it is in a mild environment, such as room temperature and pressure, and no special reagents exist. The chemical bonds between the atoms in the molecule can maintain a relatively stable state, and it is not easy to break or rearrange.
However, it should be noted that if the environmental conditions change, such as increasing the temperature, introducing specific catalysts or strong acid-base reagents, its stability may also be damaged. Under high temperatures, the thermal motion of the molecule intensifies, the vibration of the chemical bond increases, or some relatively weak chemical bonds are broken, which may lead to chemical reactions. Strong acid-base environments may also react with amino groups or carboxylic acid anhydride structures, causing their chemical properties to change. In general, the chemical properties of 3-aminoindole-2-carboxylic anhydride are relatively stable under conventional chemical operation and storage conditions, but it still has certain reactivity under certain conditions.
What is the preparation method of 3-aminopyrazine-2-carboxylate?
To prepare 3-aminopyridine-2-carboxylic anhydride, the method is as follows:
First take an appropriate amount of 3-aminopyridine-2-carboxylic acid and place it in a clean reaction vessel. Slowly add an appropriate amount of dehydrating agent to it, common such as acetic anhydride, phosphorus pentoxide, etc. Taking acetic anhydride as an example, the two interact, and the acyl group of the anhydride binds to the hydroxyl group of the carboxyl group in the acid to remove a molecule of acetic acid.
When reacting, the temperature needs to be controlled within an appropriate range. Due to high temperature, side reactions can easily occur and the product is impure; if the temperature is too low, the reaction rate will be slow In general, when the temperature is controlled under moderate heating, slight bubbles can be observed escaping from the container, and the solution gradually becomes slightly boiling, which is a sign of the reaction.
And during the reaction process, it is necessary to continuously stir to make the reactants fully contact, speed up the reaction process, and make the reaction more uniform. Stirring can be made with the help of a magnetic stirrer to make the stirring rate stable and controllable.
When the reaction is completed, the reaction mixture contains the desired 3-aminopyridine-2-carboxylic acid anhydride. At this time, separation and purification are required. The method of vacuum distillation can be used first to remove the unreacted dehydrating agent and other low boiling point impurities. Then, a suitable organic solvent is recrystallized. Common organic solvents such as ethanol and ether are selected to be suitable for the solubility characteristics of the product. After several recrystallization, pure 3-aminopyridine-2-carboxylic anhydride can be obtained.
This preparation method requires attention to the details of each step. The amount of dehydrating agent, the control of reaction temperature and time, and the accuracy of separation and purification are all related to the purity and yield of the product.
What is the price range of 3-aminopyrazine-2-carboxylate in the market?
3-Hydroxypyridine-2-carboxylic anhydride is in the market, and its price is between 100 gold and 1000 gold. Both of these are used in organic chemistry, and the preparation is not easy. The required raw materials and processes are quite exquisite, so the price is not cheap.
3-Hydroxypyridine-2-carboxylic anhydride, the synthesis path needs to start with a specific pyridine derivative, obtained through multi-step reaction. The reaction conditions are harsh, the temperature and pH are precisely controlled, and the reagents used are also carefully selected. If there is a slight poor pool, the product will be impure, which will damage its quality and efficiency, and the cost will remain high.
In the field of chemical and pharmaceutical research and development, 3-hydroxypyridine-2-carboxylic anhydride has a wide range of uses. In pharmaceutical creation, it is a key intermediate for the synthesis of specific drugs, which can help R & D personnel create new drugs with unique structures and excellent curative effects; in chemical production, it can contribute to the preparation of polymer materials with special properties. The key to its use makes the demand constant, and the price is stable in the range of 100 gold to 1000 gold.
Although the price is high, due to its irreplaceable effectiveness in various fields, many industry players are willing to spend a lot of money to buy, so as to become their own R & D and production.