2 Chloro 5 Iodophenyl 4 3s Tetrahydro 3 Furanyl Oxy Phenyl Methanone

(2-Chloro-5-iodophenyl) (4- (((3S) -tetrahydro-3-furanyl) oxy) phenyl) methanone, the chemical structure of this compound, let me describe in detail.
First of all, looking at its name, "methanone" indicates that this compound contains a carbonyl group (C = O), and two hydrocarbon groups are connected at both ends of the carbonyl group. " (2-chloro-5-iodophenyl) " means that on a benzene ring, the 2nd carbon position is connected with a chlorine atom, and the 5th carbon position is connected with an iodine atom.
And the " (4- ((3S) -tetrahydro-3-furanyl) oxy) phenyl) " part indicates that the No. 4 carbon position of another benzene ring is connected to a tetrahydrofuran group through an oxygen atom. Among this tetrahydrofuran group, No. 3 carbon has chirality and the configuration is S.
Overall, its chemical structure is based on methanone as the core, and the two sides are connected to specific substituted benzene ring structures. This combination of structures endows this compound with unique chemical properties and potential applications. In this way, the chemical structure of (2-chloro-5-iodophenyl) (4- ((3S) -tetrahydro-3-furanyl) oxy) phenyl) methanone is outlined.

The physical properties of (2-chloro-5-iodophenyl) (4- ((3S) -tetrahydro-3-furanyl) oxy) phenyl) methanone are of great value for investigation. The morphology of this compound, at room temperature and pressure, or in the state of solid state, or in the state of crystallization, crystal shape or regular order, or slightly uneven, depending on the preparation method and conditions.
When it comes to color, it is generally colorless to yellowish. If impurities are mixed in during the preparation process, the color may be slightly darker. Its melting point is also an important physical property, but the exact value needs to be determined by precise experiments. It is presumed that its melting point may be in a certain temperature range, which is related to the intermolecular force and crystal structure. Those with strong intermolecular force may have a higher melting point; those with high crystal structure regularity will also help to increase the melting point.
In terms of solubility, in organic solvents, there may be different performances. Common organic solvents, such as ethanol, acetone, etc., have different degrees of solubility. In ethanol, there may be a certain solubility. Because the polarity of ethanol is compatible with the polarity of the partial structure of the compound, the intermolecular force interaction can be used to promote dissolution. In non-polar solvents such as n-hexane, the solubility may be extremely low, because the non-polarity is contrary to the structure of the compound, and it is difficult to interact between molecules.
Density is also a physical property that cannot be ignored. Although the exact density needs to be measured by professional instruments, the density range can be preliminarily inferred according to its structure and the laws of similar compounds. The relative atomic mass of chlorine and iodine atoms in the molecule is relatively large, or the overall density is higher than that of ordinary organic compounds.
The physical properties of this compound are all key guidelines for its synthesis, separation, purification and application, which is the focus of research.

To prepare (2-chloro-5-iodophenyl) (4- (((3S) -tetrahydro-3-furanyl) oxy) phenyl) methanone, the following method can be used.
First take the appropriate starting material, react 2-chloro-5-iodobenzoic acid with the appropriate reagent to prepare the corresponding acid chloride. In this process, mild reaction conditions should be selected, and the reagent used should be dry and anhydrous to prevent side reactions from occurring. For example, thionyl chloride is used as an acylating agent, in an appropriate solvent, such as dichloromethane, heated and refluxed to convert benzoic acid into acyl chloride, and the product is purified by reduced pressure distillation.
At the same time, another 4-hydroxyanisole is taken and reacted with (3S) -tetrahydro-3-furan halide (such as (3S) -tetrahydro-3-furan bromide) under basic conditions. Potassium carbonate is often used as a base, and in polar aprotic solvents such as N, N-dimethylformamide, heated and stirred to promote the formation of ether bonds. After the reaction is completed, the pure 4- ((3S) -tetrahydro-3-furanyl) oxy) anisole is obtained by extraction, column chromatography and other means.
Then, the obtained acyl chloride is combined with 4- ((3S) -tetrahydro-3-furanyl) oxy) anisole, and the Fu-g acylation reaction is carried out in the presence of a catalyst. Using anhydrous aluminum trichloride as a catalyst, acid chloride is slowly added dropwise at low temperature in a solvent such as dichloromethane. After the reaction is completed, the target product (2-chloro-5-iodophenyl) (4- ((3S) -tetrahydro-3-furanyl) oxy) phenyl) methanone can be obtained through hydrolysis, neutralization, extraction, drying, column chromatography and other steps.
In each step of the reaction, the reaction temperature, time and reagent dosage need to be precisely controlled, and the product in each step needs to be strictly purified to ensure the purity and yield of the final product.

(2-Chloro-5-iodophenyl) (4- ((3S) -tetrahydro-3-furanyl) oxy) phenyl) methanone, this compound has potential applications in many fields.
In the field of pharmaceutical research and development, its structural properties may endow unique biological activities and can be used as lead compounds. By modifying and optimizing its structure, it is expected to create novel drugs, such as targeting specific disease-related targets, or having anti-inflammatory and anti-tumor effects, which can contribute to human health and well-being.
In the field of materials science, because it contains special functional groups and structures, it may be used to prepare materials with special properties. Such as participating in polymer synthesis, changing the optical, electrical and other properties of materials, in optoelectronic devices, such as organic Light Emitting Diode (OLED), solar cells and other fields, through rational design and application, may improve device performance and efficiency.
In the field of organic synthetic chemistry, it is an important intermediate. With its multi-functional group properties, it can undergo various chemical reactions to build complex organic molecular structures, providing the possibility for the synthesis of more valuable compounds, promoting the development of organic synthetic chemistry, expanding the compound library, and providing a material basis for the development of various fields.

Now there are (2-chloro-5-iodophenyl) (4- (((3S) -tetrahydro-3-furanyl) oxy) phenyl) methanone, and I would like to know what its market prospects are. This is a fine chemical in the field of organic chemistry, and its prospects are related to many factors. Let me tell you one by one.
From the perspective of application, it may have important uses in the field of pharmaceutical research and development. Or it is a key intermediate for the synthesis of new drugs, helping to create specific drugs for specific diseases. There is a strong demand for innovative drugs in today's pharmaceutical market. If this compound can play a unique role in the drug synthesis path and provide assistance for the treatment of difficult diseases, the market prospect is quite promising. Many pharmaceutical companies have invested a lot of resources to explore such key intermediates in order to promote the drug research and development process.
Furthermore, in the field of materials science, or because of its special molecular structure, it exhibits unique physical and chemical properties, which are suitable for the preparation of specific functional materials. For example, in the fields of optical materials, electronic materials, etc., it may endow materials with novel properties and meet the needs of high-end technology industries for special materials. With the rapid development of science and technology, the demand for high-performance materials is increasing day by day. If it can meet the requirements of related fields, it will also open up a broad market space.
However, its market prospects are also facing challenges. The difficulty of synthesizing this compound requires precise control of the reaction conditions to ensure the purity and yield of the product. If the cost of synthesis is too high, it may be limited due to marketing activities or price factors. In addition, market competition is also a key factor. If the same or alternative compounds have occupied a certain market share, in order to stand out, they need to highlight their own advantages, such as higher activity and better stability.
In summary, the (2-chloro-5-iodophenyl) (4- ((3S) -tetrahydro- 3-furanyl) oxy) phenyl) methanone market prospects have both opportunities and challenges. If we can break through the bottleneck of the synthesis process, reduce costs, and fully exploit its unique performance advantages to effectively cope with competition, we will be able to win a place in the market and have a promising future. On the contrary, if we cannot overcome many difficulties, we may face difficulties in the development of the market.