What is the chemical structure of (1s) -1,5-anhydro-2,3,4,6-tetrakis- o- (2,2-dimethylpropanoyl) -1- (3- {[5- (4-fluorophenyl) thiophen-2-yl] methyl} -4-methylphenyl) -d-glucitol

This is the chemical nomenclature of an organic compound. To clarify its chemical structure, it is necessary to gradually analyze it according to the nomenclature. " (1S) -1,5-dehydrated-2,3,4,6-tetra-O- (2,2-dimethylpropionyl) -1 - (3 - {[5- (4-fluorophenyl) thiophene-2-yl] methyl} -4 -methylphenyl) -D-glucositol". " (1S) " indicates that the configuration of the chiral center of the compound is S-type. " 1,5-Dehydration "Water is lost between the 1-position and the 5-position carbon atoms in the epitomal structure to form a cyclic structure." 2,3,4,6-tetra-O- (2,2-dimethylpropionyl) "means that the hydroxyl groups at the 2,3,4,6 positions are esterified with 2,2-dimethylpropionyl groups to form corresponding ester groups." 1 - (3 - {[5- (4-fluorophenyl) thiophene-2-yl] methyl} -4 -methylphenyl) "indicates that the carbon atom at 1 position is connected to a complex aryl structure, in which the thiophene ring is connected to 4-fluorophenyl at 5 position, and the thiophene ring at 2 position is connected to the benzene ring at 3 position through methylene, and the benzene ring at 4 position has methyl. Overall, the core of the compound is a glucositol structure, which has been modified in many places, such as dehydration to form rings, esterification, and the introduction of complex aryl groups, resulting in this specific chemical structure with unique chemical and physical properties.

What are the physical properties of (1s) -1,5-anhydro-2,3,4,6-tetrakis- o- (2,2-dimethylpropanoyl) -1- (3- {[5- (4-fluorophenyl) thiophen-2-yl] methyl} -4-methylphenyl) -d-glucitol

This is 1 - (1S) - 1,5 - dehydrated - 2,3,4,6 - tetra- O - (2,2 - dimethylpropionyl) - 1 - (3 - {[5 - (4 - fluorophenyl) thiophene - 2 - yl] methyl} - 4 - methylphenyl) - D - glucitol, which is an organic compound. Its physical properties are as follows:

From the perspective, this compound may be in the form of a white to off-white powder. Due to the characteristics of its molecular structure, the intermolecular forces make the microscopic particles arranged in an orderly manner, and the external morphology is stable.

Its melting point and boiling point are related to the intermolecular force and structural stability. Many groups in the molecule affect the intermolecular force, so the melting point may be within a specific range. The interaction between groups restricts the thermal movement of molecules, so the melting point is reflected. The boiling point is also determined by factors such as intermolecular force and relative molecular weight.

In terms of solubility, due to the presence of polar groups and non-polar parts, the solubility is different in polar solvents such as water and non-polar solvents such as alkanes. Polar groups make compounds have a certain solubility in polar solvents, while non-polar parts limit their solubility in water, and solubility is better in non-polar solvents.

Density is determined by the relative mass of molecules and the way molecules are deposited. Its molecular structure is established, the relative mass of the molecules is certain, and the packing tightness affects the density.

The physical properties of this compound are determined by its unique molecular structure, and the groups in the structure interact to exhibit the above physical properties together.

What is the synthesis method of (1s) -1,5-anhydro-2,3,4,6-tetrakis- o- (2,2-dimethylpropanoyl) -1- (3- {[5- (4-fluorophenyl) thiophen-2-yl] methyl} -4-methylphenyl) -d-glucitol

To prepare (1s) -1,5 -dehydrated -2,3,4,6 -tetra- o- (2,2 -dimethylpropionyl) -1 - (3- {[5- (4 -fluorophenyl) thiophene-2 -yl] methyl} -4 -methylphenyl) -d -glucitol, the method is as follows:

First take an appropriate amount of glucose alcohol-containing starting material and place it in a suitable reaction vessel. In an anhydrous environment and with proper temperature control, add an appropriate amount of 2,2-dimethylpropionylation reagent, such as 2,2-dimethylpropionyl chloride, and add an appropriate amount of acid binding agent, such as pyridine, etc., so that it fully reacts, so that the 2,3,4,6 hydroxyl groups of glucitol are all dimethylpropionylated to obtain the corresponding tetra- o- (2,2-dimethylpropionyl) intermediate. < Br >
Then, prepare another reagent containing 3- {[5- (4-fluorophenyl) thiophene-2-yl] methyl} -4 -methylphenyl, and combine this reagent with the above-mentioned intermediate. Under the action of a matching catalyst, in a suitable organic solvent, through a condensation reaction, the 1-hydroxyl group is connected to the phenyl reagent.

After the reaction is completed, the product is separated and purified by conventional post-treatment methods such as extraction, washing, and drying. Extraction can be carried out with a suitable organic solvent, such as dichloromethane, etc.; washing to remove impurities; drying with a desiccant such as anhydrous sodium sulfate. Finally, by means of column chromatography or recrystallization, it can be further purified with high purity of (1s) -1,5-dehydrated-2,3,4,6-tetra-o- (2,2-dimethylpropionyl) -1 - (3- {[5- (4-fluorophenyl) thiophene-2-yl] methyl} -4 -methylphenyl) -d -glucitol. The whole process requires fine temperature control and control, and pay attention to the dosage of each reagent to ensure the smooth reaction and obtain the desired product.

What are the application fields of (1s) -1,5-anhydro-2,3,4,6-tetrakis- o- (2,2-dimethylpropanoyl) -1- (3- {[5- (4-fluorophenyl) thiophen-2-yl] methyl} -4-methylphenyl) -d-glucitol

This is an organic compound with a rather complex structure, named (1S) -1,5-dehydration-2,3,4,6-tetra-O- (2,2-dimethylpropionyl) -1- (3- {[5- (4-fluorophenyl) thiophene-2-yl] methyl} -4-methylphenyl) -D-glucitol. It has potential applications in many fields.

In the field of pharmaceutical research and development, it may exhibit specific biological activities due to its unique chemical structure. Or it can be used as a lead compound, which has been deeply studied and optimized to explore drugs with therapeutic effects on diseases. Or it has a certain effect on some disease-related targets. By interacting with the targets, it regulates the physiological processes in the organism to achieve the purpose of treating diseases.

In the field of organic synthetic chemistry, the complex structure of this compound brings challenges and opportunities to synthetic chemists. The process of synthesizing this compound requires a series of exquisite organic synthesis methods and strategies to promote the development of organic synthesis technology. It can also provide reference and ideas for the synthesis of other complex natural products or functional molecules.

In the field of materials science, if this compound is appropriately modified or combined with other materials, it may endow the material with specific properties. Or improve the optical, electrical, thermal and other properties of the material, and find applications in optoelectronic materials, polymer materials, etc.

In summary, (1S) -1,5-dehydration-2,3,4,6-tetra-O- (2,2-dimethylpropionyl) -1- (3- {[5- (4-fluorophenyl) thiophene-2-yl] methyl} -4-methylphenyl) -D-glucitol has potential application value in many fields such as medicine, organic synthesis and materials science, and is worthy of in-depth exploration and exploration.

What is the market outlook for (1s) -1,5-anhydro-2,3,4,6-tetrakis- o- (2,2-dimethylpropanoyl) -1- (3- {[5- (4-fluorophenyl) thiophen-2-yl] methyl} -4-methylphenyl) -d-glucitol?

Today there is a product named (1S) -1,5 -dehydrated-2,3,4,6 -tetra-O- (2,2 -dimethylpropionyl) -1 - (3- {[5- (4 -fluorophenyl) thiophene-2 -yl] methyl} -4 -methylphenyl) -D -glucitol. The prospect of this substance in the market is quite interesting.

At present, although this compound is not widely known, it has potential in fields such as pharmaceutical research and development. Because of the journey of medicine, new substances are often sought to solve difficult diseases. Its unique chemical structure may interact with biomolecules in the body, opening up new therapeutic paths.

Furthermore, in the fields of materials science, new compounds are also often a source of innovation. Its physical and chemical properties may give rise to new materials, which can be applied in many ways. Although the current market has not seen its great popularity, in time, if researchers can deeply explore its properties and uses, it may open up new market space and trigger changes in related fields. Therefore, although its market prospects are uncertain, it is expected to emerge in scientific exploration and industrial development in the future.