2 Thiophenecarboxylic Acid 4 Methyl 3 1 Oxo 2 Propylamino Propyl Amino Methyl Ester Monohydrochloride
Quinoline Thiophene Imidazole Thiazole
2-Thiophenecarboxylic acid, 4-methyl-3-((1-oxo-2-(propylamino)propyl)amino)-, methyl ester, monohydrochloride
Chemical Formula C15H23ClN2O3S
Molecular Weight 346.87
Appearance Solid (predicted)
Solubility Soluble in organic solvents (estimated)
Logp Value related to lipophilicity, estimated based on structure
Vapor Pressure Low (estimated for a solid compound)
Density Estimated value based on similar organic esters
FAQ

2-Thiophenecarboxylic acid, 4-methyl-3- ((1-oxo-2- (propylamino) propyl) amino) -, methyl ester, monohydrochloride

This compound is called 2-thiophenecarboxylic acid, 4-methyl-3- ((1-oxo-2- (alanyl) propyl) amino) -, methyl ester, monohydrochloride. In the ancient classical Chinese genre of "Tiangong Kaiwu", its chemical structure is described as follows:

This compound, based on thiophene, is added with a carboxyl group at the second position to form a genus of thiophenecarboxylic acid. In the fourth position, methyl is set to change its properties. And in three places, a long chain is connected. The chain head is a carbonyl group, the ortho-position of the carbonyl group, connected with the alanyl group, and the alanyl group is the shape of the contact between the propyl group and the amino group. At the end of this chain, an amino group is attached, and this amino group is conjugated with the structure of methyl ester, that is, the methyl ester group is attached to the end of the long chain connected by the three-position thiophene ring. In addition, this compound is still combined with monohydrochloride to form a hydrochloride state. In this structure, the chain phase is named, and the functional groups are staggered, forming this unique chemical body with its specific physical and chemical properties and reactivity.

What are the main uses of 2-Thiophenecarboxylic acid, 4-methyl-3- ((1-oxo-2- (propylamino) propyl) amino) -, methyl ester, monohydrochloride

2-Thiophenecarboxylic acid, 4-methyl-3- (1-oxo-2- (propylamino) propyl) amino) -, methyl ester, monohydrochloride This substance is widely used. In the field of medicine, it can be used as a key intermediate to help synthesize various specific drugs. Due to its special chemical structure, it can precisely fit with many targets in organisms, or participate in the regulation of specific physiological processes, or modify abnormal physiological activities related to diseases, thus providing an indispensable basis for drug development.

In the chemical industry, it also has extraordinary performance. It can be used as an important raw material for the synthesis of special materials, and is converted into materials with unique properties through a series of chemical reactions. For example, in the synthesis of some polymer materials, after adding this substance, the stability, flexibility and other properties of the material can be significantly improved, thus meeting the strict requirements of material properties in different industrial scenarios.

In the field of scientific research and exploration, 2-thiophenecarboxylic acid, 4-methyl-3- (1-oxo-2 - (propyl amino) propyl) amino) -, methyl ester, and monohydrochloride are often used as research model compounds. Through in-depth investigation of their properties and reaction mechanisms, researchers can further clarify the basic theories of related chemical fields, providing valuable theoretical basis and practical experience for the design and synthesis of new compounds and the opening up of new reaction paths, and promoting the continuous development of chemistry.

What are the physical properties of 2-Thiophenecarboxylic acid, 4-methyl-3- ((1-oxo-2- (propylamino) propyl) amino) -, methyl ester, monohydrochloride

2-Thiophenecarboxylic acid, 4-methyl-3- ((1-oxo-2- (alanyl) propyl) amino) -, methyl ester, monohydrochloride, this physical property belongs to the category of organic compounds. Its appearance is often solid, because organic salts are mostly solid. In terms of solubility, the compound contains polar groups, such as carboxyl-derived ester groups, amino groups and their hydrochloride parts, so it may have a certain solubility in polar solvents, such as water and alcohols, but poor solubility in non-polar solvents such as alkanes. The melting point of

is a specific temperature, which is the critical temperature for the substance to change from solid to liquid, which is of great significance for its identification and purity judgment. Its stability is closely related to its structure, and the thiophene ring in the molecule is an aromatic structure, which has a certain stability; however, the amino group and ester group part may affect the overall stability due to chemical reaction activity, and may react under acid-base conditions. For example, ester groups can be hydrolyzed by acid or base catalysis, and amino hydrochloride will free out amino groups in alkaline environments. In addition, due to the presence of multiple reactive groups, the compound has certain chemical reactivity and can participate in a variety of organic reactions, such as acylation and alkylation of amino groups, and ester groups can participate in ester exchange reactions. Therefore, it may have potential application value in the field of organic synthesis.

What is the synthesis method of 2-Thiophenecarboxylic acid, 4-methyl-3- ((1-oxo-2- (propylamino) propyl) amino) -, methyl ester, monohydrochloride

To prepare 2-thiophenecarboxylic acid, 4-methyl-3- ((1-oxo-2- (propylamino) propyl) amino) -, methyl ester, monohydrochloride, you can follow the following methods.

First take a suitable thiophene derivative as the starting material, add a specific reagent and catalyst in a suitable reaction vessel. With fine operation, the starting material and reagent react under certain temperature and pressure conditions. This reaction aims to modify the thiophene ring and introduce a specific substituent.

Then, a series of reaction steps are carried out for the generated intermediate product. By adjusting the reaction environment, such as changing the reaction temperature, pH, etc., to further guide the structural transformation of the intermediate product to the target product. In this process, it is particularly crucial to precisely control the reaction at each step to prevent the excessive occurrence of side reactions.

Next, at the right time, a methyl ester group is introduced. This step requires the selection of appropriate esterification reagents and reaction conditions to ensure that the methyl esterification reaction is carried out efficiently and accurately.

Finally, when the main structure of the target product is formed, an appropriate amount of hydrochloric acid is added through specific acidification methods to obtain the hydrochloric acid form of the target product. The whole synthesis process requires experimenters to be familiar with the mechanism and operation skills of various organic reactions, and to fine-tune the reaction parameters of each step to obtain higher yields and purity of 2-thiophenecarboxylic acid, 4-methyl-3- (1-oxo-2- (propylamino) propyl) amino) -, methyl ester, monohydrochloride.

2-Thiophenecarboxylic acid, 4-methyl-3- ((1-oxo-2- (propylamino) propyl) amino) -, methyl ester, monohydrochloride

Today, there are 2-thiophenecarboxylic acid, 4-methyl-3- ((1-oxo-2- (alanyl) propyl) amino) -, methyl ester, and monohydrochloride, and their market prospects are related to many aspects.

Looking at all kinds of new things in the past, if you want to be widely distributed in the city, the first use is its use. This compound may be used in the field of medicine as a raw material for the creation of new agents. With its unique structure, it may be able to target specific diseases and have significant curative effects. In this way, it is expected to be favored by the pharmaceutical industry, and the market prospect is considerable. For example, in the past, many newly developed drug ingredients, because they can solve the suffering of patients, have a wide market and generate considerable profits.

Furthermore, consider the difficulty and cost of synthesis. If the synthesis method is cumbersome, consumes huge resources, and the cost is high, it will hinder marketing activities. On the contrary, if the synthesis is convenient and the cost is controllable, it will be able to attract more manufacturers to invest in production, improve market supply, and then expand the market. Just like the ancient skills, simple and efficient ones can spread far and wide.

Again, the market competition situation is also the key. If this compound is in a field where there are many competing products, and each is good at winning, it needs to rely on its own advantages, such as unique efficacy and better quality, to stand out. And if there is no strong opponent, the market prospect will be brighter.

Also, the direction of policies and regulations cannot be ignored. In the field of pharmaceutical and chemical industry, policy supervision is strict. If this compound meets the requirements of regulations and obtains relevant licenses smoothly, its market road will be smoother. Otherwise, even if there are good materials and beautiful quality, it will be difficult to market.

Overall, 2-thiophenecarboxylic acid, 4-methyl-3- ((1-oxo-2 - (alanyl) propyl) amino) -, methyl ester, monohydrochloride, if it can be properly addressed in terms of use, cost, competition and policy, and seize the opportunity, its market prospect may be as bright as spring flowers, promising; otherwise, it may encounter thorns and face difficulties in moving forward.