Methyl 2 3 Morpholin 4 Yl Propanoyl Amino 4 5 6 7 Tetrahydro 1 Benzothiophene 3 Carboxylate
Quinoline Thiophene Imidazole Thiazole
methyl 2-{[3-(morpholin-4-yl)propanoyl]amino}-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxylate
Chemical Formula C20H28N2O5S
Molar Mass 412.51 g/mol
Appearance Typically solid (but dependent on purity and conditions)
Solubility In Water Limited solubility (due to its organic nature)
Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform
Logp Estimated to be positive, indicating lipophilicity
FAQ

What is the chemical structure of methyl 2- {[3- (morpholine-4-yl) propionyl] amino} -4,5,6,7-tetrahydro-1-benzothiophene-3-carboxylate?

There is a question about the chemical structure today, which is related to methyl 2 - {[3 - (fluorescence - 4 - group) propionitrile] oxo} -4,5,6,7 - tetrahydro - 1 - naphthalimidazole - 3 - carboxylic anhydride. This is a question about a complex structure in chemistry, and I should use the text of "Tiangong Kaiwu" to solve it.

Looking at this structure, methyl is a simple group of hydrocarbons, which is connected to the subsequent complex group with the position of "2 -". In square brackets, "3- (fluorescent-4-yl) propionitrile", the fluorescent group has unique optical properties, and the propionitrile contains a cyanide group. The two are connected to the "3-" position to show their spatial and chemical properties. Then followed by "oxygen generation", this oxygen atom is connected to the front and rear groups with its unique valence bond, which affects the overall chemical activity.

As for "4,5,6,7-tetrahydro-1-naphthalimidazole-3-carboxylic anhydride", the naphthalimidazole structure is a fused ring system, and the tetrahydro indicates that some of its unsaturated bonds are formed by hydrogenation, which gives the molecule specific rigidity and stability. " 3-Carboxylic anhydride ", the functional group of carboxylic anhydride has high reactivity and can participate in a variety of organic reactions.

Overall, this chemical structure fuses a variety of functional groups and special structures, and its overall properties are determined by the cooperation of each part. The spatial arrangement and electronic effect interaction between the groups make this compound have unique application potential in chemical synthesis, materials science and other fields. Its fluorophore group may be used for optical detection, carboxylic anhydride can be used as an intermediate in organic synthesis reactions, and the naphthalene imidazole structure may provide a certain biological activity basis. The unique structure of this compound makes it an object worthy of further investigation in chemical research.

What are the main physical properties of methyl 2- {[3- (morpholine-4-yl) propionyl] amino} -4,5,6,7-tetrahydro-1-benzothiophene-3-carboxylate?

"Tiangong Kaiwu" says: The two groups are different in their properties. Among them, the [3- (phosphor-4-yl) propionitrile] oxygen group is a special structure. Its related substances with 4,5,6,7-tetrahydro-1-naphthalimidazole-3-carboxylic anhydride each have their own unique physical properties.

Methyl itself has a certain stability. Because of its hydrocarbon structure, it is not easy to react violently with ordinary things. However, when it is connected to a specific group, such as the above complex structure, the properties will change. < Br >
[3- (phosphor-4-yl) propionitrile] oxy group, due to the introduction of phosphor-related groups, or to make this material have certain fluorescence characteristics, it can emit light in a specific environment. This is due to the conjugated structure of the phosphor group, which can absorb and emit light of a specific wavelength.

4,5,6,7-tetrahydro-1-naphthalene imidazole-3-carboxylic acid anhydride, its physical properties can also be investigated. Due to the structure of tetrahydronaphthalene, it is given a certain lipid solubility and can be soluble in some organic solvents. The presence of the imidazole ring makes this substance alkaline to a certain extent, and can react with acids to form corresponding salts. The structure of carboxylic anhydride is chemically active, and it is prone to hydrolysis, alcoholysis and other reactions to generate corresponding carboxylic acids or esters.

In summary, these compounds exhibit diverse physical properties due to the synergistic effect of various groups, which are of great significance in chemical research and practical applications. They can be used in the preparation of fluorescent materials, pharmaceutical intermediates and many other fields, contributing to the development and application of chemistry.

What are the common synthesis methods of methyl 2- {[3- (morpholine-4-yl) propionyl] amino} -4,5,6,7-tetrahydro-1-benzothiophene-3-carboxylate?

"Tiangong Kaiwu" has a saying: "Most of the casters use the method of iron to turn pig iron into wrought iron, and the method is different." Now on the common synthesis methods of methyl 2- {[3- (fluorescent-4-yl) propionitrile] benzyl} -4,5,6,7-tetrahydro-1-naphthalimidazole-3-carboxylic anhydride, there are also many.

One, can start from aromatic hydrocarbons containing corresponding substituents, and introduce halogen atoms through halogenation reaction. If a specific aromatic hydrocarbon reacts with a halogenated reagent under suitable conditions, a specific position on the aromatic ring can be replaced by a halogen atom. Then, the nucleophilic substitution reaction is used to replace the halogen atom with a nitrile-containing group to form the precursor of the 3- (fluorescent-4-yl) propionitrile moiety. Then, by reacting with a benzyl-containing reagent, a benzyl-linked structure is constructed. Finally, through a series of cyclization, dehydration and other reactions, a cyclic structure of the methyl body is formed, and a carboxylic anhydride group is introduced. This process requires precise control of the reaction conditions, such as temperature, reaction time, and reagent dosage, to ensure the yield and selectivity of each step of the reaction.

Second, the strategy of functional group conversion can also be used from compounds with partial target structures. For example, first select a compound containing a similar skeleton, and gradually convert some of its functional groups into the desired methyl 2 - {[3 - (fluorophore-4-yl) propionitrile] benzyl} -4,5,6,7 -tetrahydro-1 - naphthalimidazole-3 - carboxylic anhydride. Classical organic reactions such as oxidation, reduction, addition, and elimination can be used to modify and modify the functional groups of the initial compounds. In this process, the reaction sequence should be reasonably designed according to the reactivity and selectivity of different functional groups to avoid unnecessary side reactions.

Third, the idea of biomimetic synthesis can also be adopted. Simulate the way of some biosynthetic compounds with similar structures in nature, and use enzymes or biocatalysts to synthesize them under milder conditions. Such methods often have the advantages of mild reaction conditions and high selectivity, but the conditions for obtaining and using biocatalysts are more demanding, and the characteristics and laws of biocatalytic systems need to be deeply studied to achieve efficient synthesis.

Methyl2- {[3- (morpholine-4-yl) propionyl] amino} -4,5,6,7-tetrahydro-1-benzothiophene-3-carboxylic acid ester has applications in what fields?

"Tiangong Kaiwu" is a great scientific and technological work in our country in ancient times, and there are many records on various technologies and material characteristics. What Wen Jun asked today involves the application field of methyl 2 - {[3 - (fluorescent - 4 - base) propionitrile] oxy} -4, 5,6,7 - tetrahydro - 1 - naphthalimidazole - 3 - carboxylic acid ester, and allow me to describe it in ancient Chinese. < Br >
This methyl 2 - {[3- (fluorescent-4-yl) propionitrile] oxy} -4, 5, 6, 7 -tetrahydro-1 -naphthalimidazole-3 -carboxylic acid ester may have wonderful uses in the field of medicine. Due to the current medical science, the structure and activity of substances are often explored in order to find a cure and save people. The unique structure of this compound may interact with specific targets in the human body. If well studied, it may be possible to obtain a good medicine for treating various diseases, such as some intractable diseases, or it may be able to find a turning point.

In the field of materials science, there may also be applications. In today's world, the performance requirements of materials are getting higher and higher, and this compound may endow materials with new characteristics due to its special chemical properties. For example, it can enhance the stability of materials, so that they can maintain good physical and chemical properties in different environments; or it can endow materials with certain optical properties, such as fluorescence properties, for use in optical displays, sensors and other fields, so that materials can play unique functions in many occasions.

Furthermore, in the field of chemical synthesis, it may be an important intermediate. Chemical synthesis often requires delicate steps and key raw materials. This compound can serve as a bridge to guide the advancement of the synthesis route, assisting chemists in preparing more complex compounds with special functions, and contributing to the development of chemical science.

In short, this methyl 2 - {[3 - (fluorescent - 4 - yl) propionitrile] oxy} -4, 5, 6, 7 - tetrahydro - 1 - naphthalimidazole - 3 - carboxylic acid ester has potential application value in many fields such as medicine, materials, chemical synthesis, etc. If it can be further studied, it will definitely bring many benefits to the progress of science and technology and the well-being of people's livelihood in the world.

What are the market prospects for methyl 2- {[3- (morpholine-4-yl) propionyl] amino} -4,5,6,7-tetrahydro-1-benzothiophene-3-carboxylate?

The side formula of Guanfu methyl is as follows :\[ -\{[( 3 - (\ text {fluorescence} - 4 -\ text {base})) \ text {propionitrile}]\ text {ethyl ester}\} - 4,5,6,7 -\ text {tetrahydro} -1 -\ text {naphthalimidazole} -3 -\ text {carboxylic anhydride}\]. As for the market prospect of this compound, it is really related to many parties.

The field of medicine may have extraordinary potential. Fluorescence-related properties may emerge in drug tracking, disease diagnosis and detection. The part of the structure of tetralin imidazole and carboxylic anhydride may be modified to fit specific targets, becoming a key precursor structure in the process of innovative drug development. The pharmaceutical market has always been in strong demand. If breakthroughs can be found in this field and new diagnostic reagents or therapeutic drugs can be developed, the prospects are promising.

Looking at the field of materials, the fluorescence properties can make it useful in optical materials. For example, fluorescent labeling materials may find applications in information storage, display technology, etc. And with the development of science and technology, the demand for new functional materials is increasing. If this compound can play its unique optical properties, it can also occupy a place in the materials market.

However, it also faces challenges. The synthesis process may need to be optimized to increase productivity and reduce costs, so as to stand out in the market competition. And marketing activities also need time, and scientific research and industry need to be closely integrated to fully release the potential value of this compound.

In summary, although there are challenges ahead, the structural characteristics of this compound make it promising in the pharmaceutical and materials markets. If good research and development is done, it will definitely be rewarded.