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What is the chemical structure of ETHYL PYRAZOLO [1,5-A] PYRIDINE-3-CARBOXYLATE
ETHYL PYRAZOLO [1,5 - A] PYRIDINE - 3 - CARBOXYLATE, the Chinese name is roughly ethyl pyrazolo [1,5 - a] pyridine - 3 - carboxylate. This is an organic compound containing a pyrazolo-pyridine parent nucleus structure. The parent nucleus is formed by fusing a pyrazolo ring with a pyridine ring, and specific atoms are connected at the fused place, giving the structure unique stability and reactivity.
It has a carboxylic acid ethyl ester group (-COOCH -2 CH
) attached to its 3 position. The ester group is active and can participate in many organic reactions, such as hydrolysis. Under acidic or basic conditions, the ester group is hydrolyzed to form carboxylic acids and ethanol; it can also carry out alcoholysis reactions and transesterification reactions with other alcohols to generate new ester compounds.
This compound has a wide range of uses in the field of organic synthesis and can be used as a key intermediate for the preparation of bioactive compounds, such as some heterocyclic drugs with potential medicinal value. Due to its unique structure and properties, it has attracted extensive attention and research in the fields of medicinal chemistry, materials science, etc. Researchers often develop compounds with novel properties by modifying and modifying their structures.
What are the main uses of ETHYL PYRAZOLO [1,5-A] PYRIDINE-3-CARBOXYLATE
ETHYL PYRAZOLO [1,5 - A] PYRIDINE - 3 - CARBOXYLATE, the Chinese name is often ethyl pyrazolo [1,5 - a] pyridine - 3 - carboxylate. This substance has a wide range of uses and is often used as a key intermediate in the field of medicinal chemistry to create various bioactive compounds. In the process of many drug research and development, it needs to build specific chemical structures, such as the synthesis of some new antibacterial and antiviral drugs. It plays a cornerstone role in the construction of complex active molecules.
In the field of pesticide chemistry, it also plays an important role. It can be chemically modified and modified to prepare pesticide products with high insecticidal, bactericidal or herbicidal properties. By precisely regulating its chemical structure, it can improve the effect of pesticides on specific targets, reduce the adverse impact on the environment, and achieve the purpose of high efficiency and low toxicity.
In the field of materials science, pyrazolo [1,5-a] pyridine-3-carboxylate ethyl ester is involved in the synthesis of functional materials, or has unique optical and electrical properties. For example, in the preparation of organic optoelectronic materials, it can adjust the material energy level structure, improve the material's light absorption and conversion efficiency, and contribute to the development of organic Light Emitting Diode, solar cells and other materials.
Overall, ETHYL PYRAZOLO [1,5 - A] PYRIDINE - 3 - CARBOXYLATE has shown great application potential in many fields such as medicine, pesticides, and materials due to its unique chemical structure and reactivity. It is like the key to opening the door to many chemical creations, injecting new vitality into the development of various fields.
What are the physical properties of ETHYL PYRAZOLO [1,5-A] PYRIDINE-3-CARBOXYLATE
ETHYL PYRAZOLO [1,5 - A] PYRIDINE - 3 - CARBOXYLATE is an organic compound, the Chinese name or ethyl pyrazolo [1,5 - a] pyridine - 3 - carboxylate. Its physical properties are described as follows:
In terms of appearance, this compound is often white to light yellow crystalline powder, with delicate appearance, uniform color and luster in pure ones, and no obvious variegation and foreign matter. This state is conducive to its precise use in various chemical reactions and preparations. Because the powder is more easily dispersed, the contact area is increased when mixed with other substances, and the reaction or mixing effect is better.
Smell it, usually without strong pungent smell, or only very weak, almost imperceptible special smell. This characteristic is very important in practical operation and application. No strong odor can avoid the irritation of the operator's sense of smell, and it will not interfere with the surrounding environment. It has obvious advantages in applications in fields with strict odor requirements such as medicine and fine chemicals.
Measure its melting point, which is about a certain temperature range. The melting point is a key indicator for identifying the purity and characteristics of the compound, and the melting point of the pure product is relatively fixed. If the melting point of the sample has a very small deviation from the theoretical value, it can be preliminarily inferred that its purity is high; on the contrary, the melting point deviation is large or contains impurities. Accurate determination of the melting point can help quality control and product identification.
Looking at its solubility, it has a certain solubility in organic solvents such as ethanol and acetone. The solubility in organic solvents provides convenience for its participation in reactions, separation and purification in chemical synthesis and drug preparation. In water, its solubility is low, which determines that its application in aqueous systems requires special consideration. For example, when designing preparations, appropriate solubilization methods need to be selected so that it can be uniformly dispersed in aqueous media to play an effect.
ETHYL PYRAZOLO [1,5 - A] PYRIDINE - 3 - CARBOXYLATE The physical properties of PYRIDINE - 3 - CARBOXYLATE are of great significance for its application and treatment in chemical engineering, pharmaceutical research and development and other fields, and need to be carefully considered and grasped.
What are the synthesis methods of ETHYL PYRAZOLO [1,5-A] PYRIDINE-3-CARBOXYLATE
ETHYL PYRAZOLO [1,5 - A] PYRIDINE - 3 - CARBOXYLATE is ethyl 1,5-diazonaphthalene-3-carboxylate, and its synthesis method is as follows:
The starting material is selected from pyridine compounds and hydrazine compounds. The two are reacted in an appropriate solvent at a suitable temperature and under the action of a catalyst, and the intermediate containing pyrazole ring structure can be formed. For example, using ethyl 3-pyridinecarboxylate and phenylhydrazine as raw materials, adding an appropriate amount of p-toluenesulfonic acid as a catalyst in ethanol solvent, and heating the reflux number, the preliminary product can be obtained. This reaction process requires close monitoring of the reaction process, and the reaction endpoint is often determined by thin layer chromatography. < Br >
After the preliminary product is obtained, it is purified through the refining step. It is generally purified by column chromatography or recrystallization. If column chromatography is selected, a suitable eluent should be carefully selected according to the polarity of the product to effectively separate the product from impurities. The recrystallization method should choose a suitable solvent to fully dissolve the product in the hot solvent, and slowly precipitate after cooling to achieve the purpose of purification.
In addition, there is another synthetic route, which is to use pyrazoles as the starting material, through carboxylation reaction, introduce carboxyl groups, and then esterify with ethanol to form the target product. For example, using pyrazolo [1,5-a] pyridine as raw material, under the action of carbon dioxide atmosphere and specific catalysts and bases, a carboxylation reaction occurs to generate pyrazolo [1,5-a] pyridine-3-carboxylic acid. After that, the carboxylic acid and ethanol are heated and refluxed under the catalysis of concentrated sulfuric acid to form 1,5-diazonaphthalene-3-carboxylate. In this process, the reaction conditions at each step need to be precisely controlled, such as temperature, reaction time, and the proportion of reactants, etc., in order to improve the yield and purity of the product.
ETHYL PYRAZOLO [1,5-A] PYRIDINE-3-CARBOXYLATE What are the precautions during storage and transportation
ETHYL PYRAZOLO [1,5 - A] PYRIDINE - 3 - CARBOXYLATE is an organic compound. During storage and transportation, many key matters must be paid attention to.
First, the storage environment should be extremely cautious. This compound should be stored in a cool, dry and well-ventilated place. If the environment is humid, or it causes moisture and deterioration, the purity and properties of the substance will be compromised due to moisture or chemical reactions. Temperature is also crucial. Excessive temperature may make the compound unstable or even trigger reactions such as decomposition; too low temperature may cause it to solidify and other conditions, which will affect the use.
Second, the packaging must be solid and stable during transportation. Choose suitable packaging materials to resist vibration, collision and friction. For example, use thick glass bottles and wrap them in foam and other cushioning materials to prevent the container from bursting due to bumps during transportation, resulting in compound leakage.
Third, clear labels are indispensable. On the storage container and transportation packaging, the name, characteristics, hazard warnings and other information of the compound should be clearly marked. In this way, the operator can quickly know its nature, and in the event of an emergency, can take effective countermeasures in time.
Fourth, isolated storage is of great significance. ETHYL PYRAZOLO [1,5 - A] PYRIDINE - 3 - CARBOXYLATE Do not mix with oxidizing substances, reducing substances or substances with very different acidity and alkalinity to prevent dangerous chemical reactions such as violent reactions, combustion and even explosions.
Fifth, compliance with regulations and standards is the basic requirement. Store and transport this compound in strict accordance with relevant national and local laws and regulations and industry standards to ensure compliance with operating practices and ensure personnel safety and environmental safety.