Ethyl 3 2 4 Carbamimidoylphenyl Amino Methyl 1 Methyl N Pyridin 2 Yl 1h Benzo D Imidazole 5 Carboxamido Propanoate Acetate
quinoline thiophene imidazole thiazole

Ethyl 3-(2-(((4-carbaMiMidoylphenyl)aMino)Methyl)-1-Methyl-N-(pyridin-2-yl)-1H-benzo[d]iMidazole-5-carboxaMido)propanoate acetate

Taiy Chemical

Specifications

HS Code

163771

Chemical Name Ethyl 3-(2-(((4-carbamoylphenyl)amino)methyl)-1-methyl-N-(pyridin-2-yl)-1H-benzo[d]imidazole-5-carboxamido)propanoate acetate
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Frequently Asked Questions
This product Ethyl 3- (2- ((4-carbamimidoylphenyl) amino) methyl) -1-Methyl-N- (pyridin-2-yl) -1H-benzo [d] imidazole-5-carboxamido) propanoate acetate what is the chemical structure
This is an organic compound named Ethyl 3- (2- ((4-carbamimidoylphenyl) amino) methyl) -1-Methyl-N- (pyridin-2-yl) -1H-benzo [d] imidazole-5-carboxamido) propanoate acetate. To clarify its chemical structure, it is necessary to disassemble and analyze this name.
"Ethyl" indicates that it contains ethyl, which is a common group of organic compounds and is connected to the molecular backbone. "3- (2- (((4-carbamimidoylphenyl) amino) methyl) -1-Methyl-N- (pyridin-2-yl) -1H-benzo [d] imidazole-5-carboxamido) " This long list describes the core part of the main structure. Among them, "1H-benzo [d] imidazole" is the parent nucleus of benzimidazole, which is a nitrogen-containing heterocycle with unique chemical properties and biological activities. "1-Methyl" epibenzimidazole ring has methyl substitution at position 1; "N- (pyridin-2-yl) " shows that the nitrogen atom is connected with 2-pyridinyl; "2- ((4-carbamimidoylphenyl) amino) methyl) " epibenzimidazole ring has a complex side chain at position 2, and the side chain contains 4-amidinophenyl and methylene structures. " 3 - carboxamido "shows that the benzimidazole ring has a formamide group at the 5th position and is connected to the third carbon atom of the main chain." Propanoate "indicates that the main chain is a propionate structure, and the ethyl group is connected to the carboxyl oxygen atom of the propionate." Acetate "indicates that the compound is in the form of acetate, that is, there is acetate in the molecule bound to it.
In summary, this compound has a complex structure, fuses a variety of groups and heterocyclic structures, and interacts with each part, giving it specific physical and chemical properties.
Ethyl 3- (2- ((4-carbamimidoylphenyl) amino) methyl) -1-Methyl-N- (pyridin-2-yl) -1H-benzo [d] imidazole-5-carboxamido) propanoate acetate
Ethyl+3-%282-%28%28%284-carbamimidoylphenyl%29amino%29methyl%29-1-Methyl-N-%28pyridin-2-yl%29-1H-benzo%5Bd%5Dimidazole-5-carboxamido%29propanoate+acetate, this is a complex organic compound named 3- (2- ((4-amidinophenyl) amino) methyl) -1-methyl-N- (pyridine-2-yl) -1H-benzo [d] imidazole-5-formamido) propionate ethyl acetate.
However, its use may exist in the field of medicinal chemistry. Cover organic compounds are often key in the creation of medicine. The structure of this compound contains many active groups, or has biological activity. For example, in combination with specific biological targets, it regulates biochemical reactions in organisms and is used for disease treatment.
In drug development, or as a lead compound. Lead compounds are compounds with specific biological activities and structures, which can lay the foundation for the development of new drugs. Researchers modify their structures to optimize activity, improve selectivity, and reduce toxicity in order to obtain better drug candidates.
In addition, in the field of organic synthesis, or as important intermediates. Intermediates can be converted into other more complex compounds through a series of chemical reactions, assisting in the construction of organic synthesis routes and expanding the variety and structure of organic compounds.
Or as tool compounds in biochemical research. Through its interaction with biomolecules, explore molecular mechanisms and signaling pathways in organisms, and provide assistance for life science research.
Ethyl 3- (2- ((4-carbamimidoylphenyl) amino) methyl) -1-Methyl-N- (pyridin-2-yl) -1H-benzo [d] imidazole-5-carboxamido) propanoate acetate
Guanfu Ethyl + 3- (2- ((4 - carbamimidoylphenyl) amino) methyl) -1 - Methyl - N- (pyridin - 2 - yl) -1H - benzo [d] imidazole - 5 - carboxamido) propanoate acetate This product, its market prospect is still unknown, as if chaos has begun, and the fog has not dissipated.
The compound has a complex structure and seems to contain endless mysteries, like a treasure hidden in the mountains, waiting to be explored by everyone. In the field of pharmaceutical research and development, it may be an opportunity to open up new paths. If one can understand the mysteries and use them skillfully, it may be able to make breakthroughs in the treatment of difficult diseases, such as clearing the clouds and seeing the sun.
However, the road to its market is also full of thorns. First, the synthesis method may require exquisite skills and complicated processes, and the high cost is like a hanging sword, restricting its large-scale production. Second, similar competitors may have seized the opportunity and have already occupied a place in the forest of the market. It is difficult to stand out.
But everything in the world is a coexistence of opportunities and challenges. If there are brave people who have the courage to invest their efforts, with perseverance, study and optimize the production process, reduce costs, and at the same time tap its unique effects to accurately locate market demand, or they can break into their own world in this chaotic market, making this product shine brightly and be used by the world, like a bright star in the night sky, illuminating a corner of the medical field.
Ethyl 3- (2- ((4-carbamimidoylphenyl) amino) methyl) -1-Methyl-N- (pyridin-2-yl) -1H-benzo [d] imidazole-5-carboxamido) propanoate acetate
To make Ethyl+3-%282-%28%28%284-carbamimidoylphenyl%29amino%29methyl%29-1-Methyl-N-%28pyridin-2-yl%29-1H-benzo%5Bd%5Dimidazole-5-carboxamido%29propanoate+acetate, there are three methods.
First, benzimidazole is used as the starting point, and methyl groups are introduced at specific positions, and then pyridyl and carboxyamide groups are introduced into the side chain through multi-step reactions. The key here is to precisely control the reaction conditions, such as temperature, pH and reaction time. Because the activity and selectivity of each step of the reaction are different, if the conditions are not appropriate, it is easy to cause side reactions to cluster and the product is impure.
Second, the core structure containing pyridyl and benzimidazole can be constructed first, and then the rest of the side chains can be added. In this way, it is necessary to make good use of coupling reactions, such as palladium-catalyzed coupling, to make each fragment precisely connected. However, this method requires very high requirements for the purity of the reactants and the activity of the catalyst, otherwise it will be difficult to meet expectations.
Third, the compound with partial structure is used as the raw material, and it is gradually modified and expanded. This requires fine planning of the reaction sequence, first for the check point reaction with high activity, and then for the relatively inert part. However, the steps of this method may be complicated, and it is necessary to patiently optimize the yield of each step.
In summary, all methods of preparing Ethyl+3-%282-%28%28%284-carbamimidoylphenyl%29amino%29methyl%29-1-Methyl-N-%28pyridin-2-yl%29-1H-benzo%5Bd%5Dimidazole-5-carboxamido%29propanoate+acetate have their own advantages and disadvantages. In actual operation, it is advisable to make careful choices and carefully optimize according to the availability of raw materials, reaction equipment and technical level to obtain pure products.
The product Ethyl 3- (2- ((4-carbamimidoylphenyl) amino) methyl) -1-Methyl-N- (pyridin-2-yl) -1H-benzo [d] imidazole-5-carboxamido) propanoate acetate What is the safety and stability of
This compound Ethyl 3- (2- ((4-carbamimidoylphenyl) amino) methyl) -1-Methyl-N- (pyridin-2-yl) -1H-benzo [d] imidazole-5-carboxamido) propanoate acetate is an extremely important issue related to its safety and stability.
When it comes to safety, this compound may have many types of latent risks. Its structure is complex, and many groups may interact with various biomolecules in organisms. For example, heterocyclic structures such as benzimidazole and pyridine can exhibit certain biological activities in some cases, or interfere with normal biochemical processes in organisms. In addition, the ethoxy group, carboxyamide group and other parts may also affect the metabolic pathway of the compound in the body, and even have toxic and side effects. However, if a rigorous toxicological evaluation is carried out, and the effects on various organs and systems of the body are investigated in detail through animal experiments, cell experiments, etc., its safety can be known for sure.
As for the stability, the stability of the compound is also influenced by a variety of factors. In terms of chemical structure, there are many chemical bonds in its molecules, such as amide bonds, benzimidazole ring and other groups. Under different environmental conditions, these chemical bonds may break or rearrange. When the temperature rises, the thermal motion of the molecule intensifies, or some chemical bonds become unstable and break. In high humidity environments, water molecules may react with compounds, causing damage to their structures. At the same time, light may also cause luminescent chemical reactions, resulting in changes in the structure of compounds. However, if storage conditions can be reasonably controlled, such as low temperature, drying, and dark storage, its stability may be effectively enhanced.