(2S)-2-[(S)-(2-Ethoxyphenoxy)(Phenyl)Methyl]Morpholine Methanesulfonate

(This is a question related to chemical structure, and it needs to be answered in the classical style of "Tiangong Kaiwu", and it is about 500 words.)
Husband (2S) -2- [ (S) - (2 -ethoxyphenoxy) (phenyl) methyl] furanaldehyde, the structure of this compound is quite complex. Looking at its names, (2S), (S), are the three-dimensional chemical configuration, which is related to the specific way of spatial arrangement of atoms in molecules.
"2 - [ (S) - (2 -ethoxyphenoxy) (phenyl) methyl]", this part describes the substituents attached to the main structure of furanaldehyde. Among them, ethoxy phenoxy group, ethoxy group, ethyl group is connected to oxygen group, connected to phenoxy group, phenoxy group is combined with phenyl group, with methyl group as a bridge, connected to furanaldehyde position No. 2.
Furanaldehyde has the structure of furan ring and aldehyde group. aldehyde-CHO, as its important functional group, has active chemical properties. Furan ring, a five-membered heterocyclic ring containing an oxygen atom, has a unique electron cloud distribution and reactivity.
As a whole, the chemical structure of this compound is composed of a specific three-dimensional configuration and an orderly combination of various groups. Each part affects each other, giving it unique physical and chemical properties. The spatial positions and electronic effects of different groups determine their performance in chemical reactions, either electrophilic, nucleophilic, or participating in various organic transformations. Such structures may be of great value in fields such as organic synthesis and drug development due to their special activities.

(2S) 2- [ (S) - (2-isopropoxyphenoxy) (phenyl) methyl] furanoic anhydride is widely used. In the field of medicine, it is often used as a key intermediate to synthesize drugs with specific physiological activities. With its unique chemical structure, it can be chemically modified and reacted to construct a variety of pharmacoactive groups, laying the foundation for the creation of new drugs and helping to develop specific drugs for specific diseases.
In the field of materials science, it can participate in the preparation of polymer materials. Due to its reactivity check point, it can polymerize with other monomers, thereby improving the properties of materials, such as improving the mechanical strength, thermal stability and solubility of materials, providing a new way for the synthesis of high-performance and multi-functional materials.
In the field of organic synthesis, (2S) -2- [ (S) - (2-isopropoxyphenoxy) (phenyl) methyl] furanoic anhydride is also an important reagent. With its structural characteristics, it can be used to catalyze or participate in a series of organic reactions, promote the synthesis and transformation of organic compounds, realize the construction of complex organic molecules, and expand the methods and strategies of organic synthesis.
This substance plays an indispensable role in many fields such as medicine, materials science, and organic synthesis, providing strong support and promotion for the development of various fields.

(2S) 2- [ (S) - (2-isopropoxyphenoxy) (phenyl) methyl] furanaldehyde, the physical properties of this substance are as follows:
Its properties may be colorless to light yellow liquid or solid, because the molecular structure contains specific functional groups and three-dimensional configurations, causing it to have certain physical properties.
In terms of melting point, due to the chiral center of the compound and the specific intermolecular force, the transition from solid state to liquid state occurs within a certain temperature range. However, the specific melting point value will vary due to factors such as purity and crystallization conditions. If the purity is high and the crystallization is good, the melting point may be relatively fixed and can be accurately determined. The boiling point of
is also affected by intermolecular forces and molecular weight. The presence of benzene ring, furan ring and alkoxy group in the molecule enhances the intermolecular van der Waals force and causes the boiling point to rise. Under normal pressure, its boiling point may be in a certain temperature range. When the external pressure changes, the boiling point also changes.
In terms of solubility, the molecule contains polar ether bonds and aldehyde groups, as well as non-polar benzene rings and furan rings, so it may be soluble in organic solvents such as ethanol, ether, and dichloromethane. The polar part can form hydrogen bonds or dipole-dipole interactions with polar solvents. There is a dispersion force between the non-polar part and the non-polar solvent, which makes it exhibit different solubility in organic solvents of different polarities. In water, because of its overall limited polarity, solubility may be poor.
Density is related to the degree of molecular packing compactness and molecular weight. Based on its molecular structure characteristics, density or in a specific range, it reflects the mass of the substance per unit volume.
Refractive index is related to the influence of molecules on light propagation. The specific molecular structure makes the speed and direction change when light propagates in it, resulting in a corresponding refractive index value. This value can be used to identify the purity and concentration of the compound.

To prepare (2S) - 2 - [ (S) - (2 - ethoxyphenoxy) (phenyl) methyl] furanal anhydride, the method is as follows:
First take an appropriate amount (2 - ethoxyphenol), dissolve it in an appropriate organic solvent, add an appropriate amount of alkali, such as potassium carbonate, stir well. Take another (bromobenzene), slowly drop into the above mixture, control the reaction temperature and drip speed, and carry out nucleophilic substitution reaction. This step aims to form (2 - ethoxyphenoxybenzene). After the reaction is completed, the pure (2 - ethoxyphenoxybenzene) is obtained by separation and purification methods, such as column chromatography.
Then, using (2-ethoxyphenoxybenzene) as raw material, with (formaldehyde) in the presence of a specific catalyst, under suitable temperature and pressure conditions, the condensation reaction is carried out to generate (2 - [ (S) - (2-ethoxyphenoxy) (phenyl) methyl] furan). After the reaction is completed, the pure product is obtained by distillation, extraction and other means.
Then the obtained (2 - [ (S) - (2 - ethoxy phenoxy) (phenyl) methyl] furan) is placed in a suitable oxidation system, such as a system composed of a specific proportion of oxidant and an organic solvent, and the oxidation reaction is carried out at a certain temperature to partially oxidize the furan ring to an acid anhydride structure, thereby preparing (2S) - 2 - [ (S) - (2 - ethoxy phenoxy) (phenyl) methyl] furanal anhydride. Finally, a high-purity target product can be obtained through fine purification steps such as recrystallization. Each step of the reaction requires precise control of the reaction conditions, paying attention to the proportion of each reactant, temperature, time and other factors, in order to make the reaction proceed smoothly and improve the yield and purity of the product.

(2S) 2- [ (S) - (2-isopropoxyphenoxy) (phenyl) methyl] furanoformamide related safety precautions are as follows:
When experimenting with this compound, the first thing to pay attention to is its chemical properties. Because its structure contains specific phenoxy, phenyl and other groups, it must be stored in a dry, cool and well-ventilated place. Because it may be sensitive to air and moisture, if stored improperly, chemical reactions may occur, causing it to deteriorate, affecting subsequent use, and even causing danger.
During operation, take good personal protection. Wear suitable protective gloves to prevent skin contact with it. Because it may be irritating, once it comes into contact with the skin, it may cause adverse reactions such as allergies, redness and swelling. At the same time, wear protective glasses and masks to avoid its powder or volatiles from entering the eyes and respiratory tract. If you are not careful to enter the eyes, you should immediately rinse with a lot of water and seek medical attention in time; if inhaled, you need to quickly move to a fresh place in the air. If you feel unwell, you should also diagnose and treat in time.
When conducting a reaction involving this compound, the reaction conditions should be precisely controlled. Factors such as temperature, pH, and reaction time all have an important impact on the reaction process and products. Unsuitable reaction conditions will not only reduce the purity and yield of the product, but may also trigger side reactions and generate dangerous substances. For example, if the temperature is too high, or the reaction is out of control, causing serious consequences such as explosion.
For the disposal of its waste, it must not be discarded at will. It should be collected and properly disposed of in accordance with relevant environmental protection regulations and laboratory regulations. Due to its special chemical properties, discarding it at will may pollute the environment and endanger the ecology.
In addition, in the place where the compound is used, it is necessary to be equipped with complete emergency equipment, such as fire extinguishers, eye washers, first aid kits, etc. In order to carry out emergency treatment in time when an emergency occurs and reduce the degree of harm.
In conclusion, when operating (2S) -2-[ (S) - (2-isopropoxyphenoxy) (phenyl) methyl] furanoformamide, attention should be paid to storage, protection, control of reaction conditions, waste disposal and emergency preparedness to ensure the safety and smooth progress of the experiment.