As a leading 4,5,6,7-Tetrahydro-1-(4-methoxyphenyl)-6-(4-nitrophenyl)-7-oxo-1H-pyrazolo[3,4-c]pyridine-3-carboxylic acid ethyl este 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 4,5,6,7-tetrahydro-1- (4-methoxyphenyl) -6- (4-nitrophenyl) -7-oxo-1H-pyrazolo [3,4-c] pyridine-3-carboxylate ethyl ester?
4,5,6,7-tetrahydro-1- (4-methoxybenzyl) -6- (4-fluorobenzyl) -7-oxo-1H-pyrazolo [3,4-c] pyridine-3-carboxylate ethyl ester, this is an organic compound. I will describe its chemical structure for you in the ancient classical text of "Tiangong Kaiwu".
The core of this compound is the ring system of pyrazolo [3,4-c] pyridine. At position 1, there is a 4-methoxybenzyl group connected. This 4-methoxybenzyl group is above the benzyl group, and is connected to a methoxy group in the para-position. At position 6, there is a 4-fluorobenzyl group, that is, the para-position of the benzyl group is substituted by a fluorine atom. At position 7, there is a monooxy group, that is, there is a carbonyl group.
At position 3 of the ring system, there is a group of ethyl carboxylate. This ethyl carboxylate is formed by esterification of the carboxyl group with ethanol.
As for the 4,5,6,7-tetrahydro, it means that the double bonds of the 4,5,6,7 positions of the pyrazolo [3,4-c] pyridine ring system are all converted into single bonds by hydrogenation reaction, and four hydrogen atoms are introduced. < Br >
The chemical structure of this compound, combined in this way, forms a unique spatial configuration and chemical properties. Each group interacts to determine its physical and chemical properties, and may have specific uses and significance in organic synthesis and related fields.
What are the physical properties of 4,5,6,7-tetrahydro-1- (4-methoxyphenyl) -6- (4-nitrophenyl) -7-oxo-1H-pyrazolo [3,4-c] pyridine-3-carboxylate ethyl ester?
4,5,6,7-tetranitrogen-1- (4-ethoxyphenyl) -6- (4-cyanophenyl) -7-oxo-1H-pyrazolo [3,4-c] pyrazole-3-carboxylate ethyl ester, this compound has unique physical properties.
Its appearance is usually crystalline solid, which is due to the interaction between molecules to promote regular arrangement. It is stable at room temperature because the chemical bonds in the molecular structure are relatively strong, but in case of high temperature, strong acid-base or specific chemical reagents, chemical reactions will occur.
In terms of solubility, in view of the fact that there are both hydrophobic phenyl groups and polar groups in the molecule, there is a certain solubility in organic solvents such as dichloromethane, N, N-dimethylformamide, and the solubility in water is low.
Melting point is an important indicator for identifying the compound. The specific molecular structure and force determine the melting point range. By accurately measuring the melting point, the purity can be judged.
In addition, the compound may have certain optical properties. For example, under specific wavelength light irradiation, the electron transition of the conjugated structure occurs, resulting in absorption or emission spectra, which has potential applications in the field of optical materials.
Its physical properties are closely related to the structure, providing the basis for its application in pharmaceutical chemistry, materials science and other fields. Understanding these properties can help researchers design experiments rationally and explore more potential uses.
What is the synthesis method of 4,5,6,7-tetrahydro-1- (4-methoxyphenyl) -6- (4-nitrophenyl) -7-oxo-1H-pyrazolo [3,4-c] pyridine-3-carboxylate ethyl ester?
To prepare 4% 2C5% 2C6% 2C7-tetrahydro-1- (4-ethoxyphenyl) -6- (4-fluorophenyl) -7-oxo-1H-pyrazolo [3,4-c] pyridine-3-carboxylic acid ethyl ester, the method is as follows:
First take an appropriate amount of 4-ethoxybenzaldehyde and fluorobenzene acetone, in a suitable reaction vessel, add base as a catalyst, control the temperature and reaction time, and promote the condensation reaction to obtain the corresponding enone intermediates. This process requires attention to the precise control of the reaction conditions. Too high or too low temperature, too long or too short time may affect the purity and yield of the product.
Then, the ketene intermediate and nitrogen-containing heterocyclic compound are cyclized under the action of specific reagents. The type and dosage of reagents used in this step have a great impact on the reaction process and product structure, so careful selection and accurate measurement are required.
Cyclization products are preliminarily treated before ethylation. Select suitable esterification reagents, such as ethanol and dehydrating agents, to convert carboxylic acids to ethyl esters under catalytic conditions. This process requires attention to the pH and dehydration effect of the reaction system to ensure the smooth progress of the esterification reaction.
After the reaction is completed, the impurities are removed by extraction, column chromatography and other separation and purification methods to refine the product. Careful operation is required in each step of separation to avoid product loss or introduction of new impurities. In this way, high purity 4% 2C5% 2C6% 2C7 -tetrahydro-1- (4-ethoxyphenyl) -6- (4-fluorophenyl) -7-oxo-1H-pyrazolo [3,4-c] pyridine-3-carboxylate ethyl ester can be obtained.
What are the application fields of 4,5,6,7-tetrahydro-1- (4-methoxyphenyl) -6- (4-nitrophenyl) -7-oxo-1H-pyrazolo [3,4-c] pyridine-3-carboxylate ethyl ester?
4,5,6,7-tetrahydro-1- (4-methoxyphenyl) -6- (4-fluorophenyl) -7-oxo-1H-pyrazolo [3,4-c] pyridine-3-carboxylate ethyl ester, this compound has important applications in medicinal chemistry, organic synthesis and other fields.
In the field of medicinal chemistry, compounds with such structures are often studied for the development of new drugs. Due to their unique molecular structure, they may have specific biological activities, such as affinity for certain disease-related targets, and are expected to be potential drugs for the treatment of diseases such as nervous system diseases, cardiovascular diseases or tumors. Researchers can modify and optimize its structure, adjust its pharmacological properties, improve the efficacy of drugs and reduce side effects.
In the field of organic synthesis, it is an important synthesis intermediate. Organic chemists can use it as a basis to further construct more complex organic molecular structures using various organic reactions, such as nucleophilic substitution reactions, redox reactions, etc. By ingeniously designing synthesis routes, different functional groups can be introduced, the types and functions of compounds can be expanded, and key synthetic building blocks can be provided for materials science, total synthesis of natural products, and other fields. At the same time, research on its synthesis methods will also help to promote the development of organic synthetic chemistry and develop more efficient and green synthesis strategies.
What is the market prospect of 4,5,6,7-tetrahydro-1- (4-methoxyphenyl) -6- (4-nitrophenyl) -7-oxo-1H-pyrazolo [3,4-c] pyridine-3-carboxylate ethyl ester?
4,5,6,7-tetranitrogen-1- (4-methoxyphenyl) -6- (4-fluorophenyl) -7-oxo-1H-pyrazolo [3,4-c] pyrazole-3-carboxylate ethyl ester, this is a promising organic compound. Looking at its market prospects, it can be analyzed from the following ends.
In the field of medicine, the unique structure of this compound may give it specific biological activities. Today, many compounds containing nitrogen heterocycles and phenyl structures have attracted much attention in drug development. For example, some compounds with pyrazole and pyrazole structures have been shown to have significant inhibitory or regulatory effects on specific disease-related targets. If this compound can exhibit similar biological activities, such as the regulation of certain inflammatory factors or the inhibition of tumor cell growth, it will have broad application space in the pharmaceutical market. At present, there is a large base of patients with inflammatory and tumor diseases. If it can be developed into drugs to meet clinical needs, its market scale is very large.
Looking at the field of pesticides, compounds containing fluorine and nitrogen heterocyclic structures often have good insecticidal and bactericidal activities. In view of the increasing demand for high-efficiency and low-toxicity pesticides in global agricultural production, if this compound is tested to have excellent control effects on common crop diseases and pests, and is environmentally friendly and has low residues, it will be able to gain a share of the pesticide market. With the advancement of green agriculture, the market share of such environmentally friendly pesticides is expected to continue to rise.
However, there are also challenges. The process of synthesizing this compound may need to be optimized to increase yield and reduce costs. And biological activity testing and safety assessment need to be rigorously carried out to meet the marketing standards of pharmaceuticals and pesticides. If the challenges can be properly met, the market prospect of this compound is quite bright, and it is expected to achieve great results in both the pharmaceutical and pesticide markets.