As a leading N-[4-[2-(2-Amino-4,7-Dihydro-4-Oxo-3H-Pyrrolo[2,3-D]Pyrimidin-5-Yl)Ethyl]Benzoyl]-L-Glutamic Acid 1,5-Diethyl Ester 4-Methylbenzenesulfonate supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.
N- [4- [2- (2-amino-4,7-dihydro-4-oxo-3H-pyrrolo [2,3-d] pyrimidine-5-yl) ethyl] benzoyl] -L-glutamic acid 1,5-diethyl ester What is the chemical structure of 4-methylbenzenesulfonate
This is an extremely complex chemical nomenclature, and in order to understand its chemical structure, it is necessary to gradually analyze it according to the nomenclature of organic chemistry.
First, the concept of "N- [4- [2- (2-hydroxy-4,7-dioxide-4-oxo-3H-imidazolo [2,3-d] pyrimidine-5-yl) ethyl] benzyl] -L-glutamic acid 1,5-diethyl ester 4-methylbenzyl ester". "N -" indicates the presence of a substituent attached to the nitrogen atom.
wherein, "[4 - [2 - (2 - hydroxy - 4,7 - dioxide - 4 - oxo - 3H - imidazolo [2,3 - d] pyrimidine - 5 - yl) ethyl] benzyl]" This part, with imidazolo [2,3 - d] pyrimidine as the core parent nucleus, at position 2 with a hydroxyl group, 4 and 7 for the oxygen generation, 5 is connected with a benzyl group with 2 - ethyl.
Furthermore, "L-glutamic acid 1,5-diethyl ester 4-methylbenzyl ester" is based on L-glutamic acid, and the carboxyl groups at the 1st and 5th positions respectively form ethyl esters, and the 4th position is connected with methylbenzyl esters.
Overall, the chemical structure of this compound is: imidazolo [2,3-d] pyrimidine is the key structure, one side is connected with a specific substituted benzyl group, and the other side is connected with a specific esterified modified L-glutamic acid through chemical bonds. Each substituent is connected to the parent nucleus in an orderly manner according to the above rules to construct the overall chemical structure.
N- [4- [2- (2-amino-4,7-dihydro-4-oxo-3H-pyrrolido [2,3-d] pyrimidine-5-yl) ethyl] benzoyl] -L-glutamic acid 1,5-diethyl ester What are the main uses of 4-methylbenzene sulfonate
This is a compound of N - [4 - [2 - (2 - hydroxy - 4,7 - dioxide - 4 - oxo - 3H - imidazolo [2,3 - d] pyrimidine - 5 - yl) ethyl] benzyl] -L - glutamine 1,5 - diethyl ester 4 - methyl benzyl ester. Its main uses are quite extensive and significant in the field of medicine.
In pharmaceutical chemistry research, such compounds are often key intermediates. Due to the presence of many special functional groups in the structure, such as hydroxyl groups, pyrimidine rings, glutamine structures, etc., it can be chemically modified and modified to develop new therapeutic drugs. For example, by virtue of the affinity of pyrimidine rings with specific biological targets, specific drugs for certain tumor cells and viral infections may be developed.
It is also of great value at the level of biochemical research. Because its structure is similar to some natural molecules in organisms, it can be used to explore cellular metabolic pathways, protein-ligand interactions, etc. For example, by leveraging its binding properties with specific proteins, the mechanism of the protein's action in cell signaling can be studied. In addition, in the field of organic synthesis, this compound can be used as a template to provide ideas and methods for the design and synthesis of organic molecules with similar structures and functions, and to promote the development of organic synthetic chemistry.
N- [4- [2- (2-amino-4,7-dihydro-4-oxo-3H-pyrrolo [2,3-d] pyrimidine-5-yl) ethyl] benzoyl] -L-glutamic acid 1,5-diethyl ester What should be paid attention to when using 4-methylbenzene sulfonate
This is a rather complex chemical called "N- [4- [2- (2-hydroxy-4,7-dioxide-4-oxo-3H-imidazolo [2,3-d] pyrimidine-5-yl) ethyl] benzyl] -L-glutamic acid 1,5-diethyl ester 4-methylbenzyl ester". When using this chemical, pay attention to the following numbers:
First, safety. Due to its complex structure, it may have unknown potential toxicity and irritation. Before use, be sure to check the relevant safety information sheet to understand its potential harm to human health, such as whether it can cause skin allergies, respiratory irritation, or chronic toxicity. When operating, it is necessary to strictly follow safety procedures and wear appropriate protective equipment, such as laboratory clothes, gloves and protective glasses, to prevent skin contact and inhalation.
Second, stability and storage. The chemical structure of this substance contains a variety of functional groups, and its stability may be affected by factors such as temperature, humidity, and light. It should be stored in a suitable environment according to its characteristics. Generally speaking, it needs to be placed in a dry, cool and dark place to prevent it from deteriorating due to environmental factors and affecting the experimental or production results.
Third, accurate measurement and operation. Due to its special structure, the measurement accuracy requirements are quite high when used. Minor measurement deviation may cause significant deviation in experimental results, or affect product quality. Therefore, it is necessary to use accurate measurement tools and operate strictly according to the experimental or production process to ensure the reliability and consistency of the results.
Fourth, compatibility considerations. When using this substance, it is necessary to consider its compatibility with other chemical substances. Due to its complex structure, or unexpected chemical reactions with certain substances, such as acid-base reactions, redox reactions, etc. Before mixing, theoretical analysis or pre-experiments should be conducted to confirm its compatibility and avoid adverse reactions.
N- [4- [2- (2-amino-4,7-dihydro-4-oxo-3H-pyrrolo [2,3-d] pyrimidine-5-yl) ethyl] benzoyl] -L-glutamic acid 1,5-diethyl ester What is the preparation method of 4-methylbenzene sulfonate
To prepare N- [4 - [2 - (2 - hydroxy-4,7 - dioxo-4 - oxo-3H - imidazolo [2,3 - d] pyrimidine-5 - yl) ethyl] benzyl] -L - glutamine 1,5 - diethyl ester 4 - methyl benzyl ester, according to the following method:
First, with suitable starting materials, the key intermediate was constructed by multi-step reaction. For example, starting with a compound containing a pyrimidine structure, under specific reaction conditions, a specific position on the pyrimidine ring is condensed with a hydroxyl-containing substituent to obtain an intermediate containing 2-hydroxy-4,7-dioxo-4-oxo-3H-imidazolo [2,3-d] pyrimidine structure. This process requires fine control of the reaction temperature, reaction time and the proportion of reactants to ensure that the reaction proceeds in the desired direction.
times, the above intermediate is reacted with a reagent containing ethyl and benzyl to form 4- [2 - (2 - hydroxy-4,7 - dioxo-4 - oxo-3H - imidazolo [2,3 -d] pyrimidine-5 - yl) ethyl] benzyl moiety. This step requires the selection of appropriate catalysts and reaction solvents to promote the efficient progress of the reaction and reduce the occurrence of side reactions.
Furthermore, L-glutamine is used as raw material, and after protecting a specific functional group with an appropriate protective group, it reacts with the obtained benzyl-containing intermediate to form N - [4 - [2 - (2 - hydroxy-4,7 - dioxo-4 - oxo-3H - imidazolo [2,3 -d] pyrimidine-5 - yl) ethyl] benzyl] -L - glutamine structure. This reaction requires strict conditions such as pH and temperature of the reaction environment and needs to be carefully regulated.
Finally, the formed product is esterified to introduce 1,5 - diethyl ester 4 - methyl benzyl ester group. This step requires the selection of suitable esterification reagents and reaction conditions. For example, under acid catalysis, the reactant is esterified with the corresponding alcohol, and purified after post-treatment. The target product N - [4 - [2 - hydroxy-4,7 - dioxo-4 - oxo-3H - imidazolo [2,3 -d] pyrimidine-5 - yl) ethyl] benzyl] -L - glutamine 1,5 - diethyl ester 4 - methyl benzyl ester. Throughout the process, after each step of the reaction, the product needs to be identified and analyzed for purity by appropriate analytical methods, such as thin-layer chromatography and nuclear magnetic resonance, to ensure the accuracy of the reaction and the quality of the product.
What is the market outlook for N- [4- [2- (2-amino-4,7-dihydro-4-oxo-3H-pyrrolo [2,3-d] pyrimidine-5-yl) ethyl] benzoyl] -L-glutamic acid 1,5-diethyl ester 4-methylbenzene sulfonate?
The name of this compound is extremely long and complex, and it is an organic substance containing specific nitrogen, oxygen and other atoms and complex groups. The relevant market prospects of this substance are influenced by a variety of factors.
From the perspective of the pharmaceutical field, its unique chemical structure or biological activity can act on specific biological targets. If it is confirmed to have pharmacological activity after in-depth research, it can be used as a lead compound for the development of new drugs. Nowadays, there is an urgent need for innovative drugs. If the compound can be optimized into an effective low-toxicity drug for difficult diseases, the market potential is huge. For example, the development of anti-cancer and neurodegenerative diseases treatment drugs, if this compound meets the needs of relevant targets, it is expected to be favored by pharmaceutical companies and bring broad market opportunities.
In the field of materials science, its special structure may endow materials with unique properties. If it can participate in the synthesis of polymer materials, it can change the mechanical, thermal and electrical properties of materials. For example, it is used to prepare high-performance engineering plastics and electronic materials, improve material properties, and meet the needs of high-end manufacturing for special materials, thus opening up new directions in the material market.
But there are also challenges in the marketing activities of this compound. Complex structures make synthesis difficult and expensive, limiting large-scale production and application. It is necessary to develop efficient and low-cost synthesis processes to reduce costs and achieve industrialization. And new compounds must be approved by strict regulations to enter the market, and a lot of time and resources need to be invested in safety and effectiveness evaluation. Only by successfully passing the approval can they enter the market for profit.