2 Chloro 5 Iodophenyl 4 S Tetrahydrofuran 3 Yl Oxy Phenyl Methanone

This is the naming of an organic compound. To clarify its chemical structure, we need to analyze the naming rules in detail. " (2-chloro-5-iodophenyl) " means that on the benzene ring, the second position is connected to the chlorine atom and the fifth position is connected to the iodine atom. "{4- [ (s) - (tetrahydrofuran-3-yl) oxy] phenyl} -methanone" means another benzene ring. The fourth position is connected to the tetrahydrofuran-3-yl of the (s) configuration by the oxygen atom, and this benzene ring is connected to the carbonyl group (represented by methanone).
According to this, its chemical structure is: the two benzene rings are connected by carbonyl groups, the first benzene ring has chlorine atoms at the second position and iodine atoms at the fifth position; the other benzene ring is connected by oxygen atoms and tetrahydrofuran-3-group of the (s) configuration. In this structure, the benzene ring is a stable aromatic structure, chlorine and iodine atoms have certain chemical activities, tetrahydrofuran-3-group also affects the properties of the compound, and the carbonyl group is one of the reactive activity checking points. Overall, this structure determines the specific physical and chemical properties of the compound, which may be of great significance in the fields of organic synthesis and medicinal chemistry.

(2-Chloro-5-iodophenyl) - {4 - [ (S) - (tetrahydrofuran-3-yl) oxy] phenyl} -methanone, the main physical properties of this substance are related to its external properties, melting boiling properties, solubility, density, etc.
First of all, it is usually a solid, multi-white or white powder, which is uniform. This substance is determined by its molecular force and temperature. The molecules are arranged in an orderly manner, resulting in a solid and powdery appearance.
In terms of melting and boiling, its melting properties are special. Due to the existence of molecules such as chlorine and iodine, the molecular force is increased, so that the melting phase is high. Therefore, the melting force is mostly due to a specific amount of energy. This is because the molecular force requires a specific energy to overcome, so that the solid solution can be overcome. The boiling force is also affected by the molecular force and the molecular weight of the phase. However, due to the consideration that it may be decomposed before the boiling, the accuracy of the boiling may be high.
In terms of solubility, this substance is different in the solution. In the solution of acetone and dichloromethane, it has a certain solubility. This is because the molecules of the soluble compound can form an even-even interaction or an even, which can help it disperse and dissolve. However, in non-soluble compounds such as n-hexane, the solubility is poor, because the molecular force of non-soluble compounds is weak, and the molecular force of breaking compounds is used to dissolve them.
Density is also an important physical property. Because its molecules contain atoms with a large atomic weight such as chlorine and iodine, the density of the phase is large, probably exceeding the density of water. This property also affects the molecular weight and atomic phase. The atomic weight and molecular density together determine its density.

To prepare (2-chloro-5-iodophenyl) - {4 - [ (s) - (tetrahydrofuran-3-yl) oxy] phenyl} -ketone, there are various methods. One common method is to start with suitable halogenated aromatics, such as 2-chloro-5-iodobenzoic acid and its derivatives, through acylation reaction, condensation with compounds containing tetrahydrofuran-3-alcohol structure. In this case, the acylation step can be assisted by acid chloride or anhydride and catalyst, such as DMAP, to make the reaction anterograde.
Alternatively, from 4- [ (s) - (tetrahydrofuran-3-yl) oxy] benzaldehyde, through the Wittig reaction or related carbonyl conversion reaction, the corresponding olefin is first obtained, and then oxidized to convert the olefin to the target methylketone structure.
Or from 2-chloro-5-iodobenzoyl chloride and 4- [ (s) - (tetrahydrofuran-3-yl) oxy] phenylboronic acid, the desired carbon-carbon bond is constructed by coupling means such as Suzuki reaction, and the final product is obtained. Each method has its own advantages and disadvantages. Reaction conditions, availability of raw materials, yield and purity all need to be considered in order to choose the best method.

(2-Chloro-5-iodophenyl) - {4 - [ (s) - (tetrahydrofuran-3-yl) oxy] phenyl} -methanone, which is useful in various fields. In the field of pharmaceutical research and development, it may be a key raw material for the creation of new drugs. Because of its unique chemical structure, it may be compatible with specific biological targets. By precisely acting on the body's biochemical pathways, it is helpful for the treatment of specific diseases, such as for some difficult diseases, or it can develop innovative therapies.
In the field of materials science, it also has applications. By virtue of its own characteristics, it may participate in the synthesis and modification of materials. After proper treatment and reaction, the material may be endowed with new properties, such as improving the stability, optical properties or electrical properties of the material, providing the possibility for the research and development of new functional materials.
Furthermore, in the field of organic synthetic chemistry, it is often used as a key intermediate. Chemists can use various organic reactions as a basis to build more complex organic molecular structures, expand the types and functions of organic compounds, promote the progress of organic synthetic chemistry, and then lay the foundation for the development of many related industries. In short, this compound has important potential application value in the fields of medicine, materials and organic synthesis, and is like the key to opening the door to various innovations, waiting for researchers to explore and explore in depth.

(2-Chloro-5-iodophenyl) - {4- [ (s) - (tetrahydrofuran-3-yl) oxy] phenyl} -methanone, this compound has a considerable market prospect at present. In the field of Guanfu pharmaceutical and chemical industry, it is like a shining star, shining with hope.
In the process of pharmaceutical research and development, many difficult diseases need to be solved urgently. And this compound, with its unique molecular structure, is like a delicate key, which is expected to open the lock of specific disease treatment. Due to the growing demand for precision targeted therapy in modern medicine, its structural characteristics may enable it to act precisely on pathogenic targets, paving the way for the creation of new drugs. Therefore, many medical research teams are paying more and more attention to it, investing a lot of effort to explore its pharmacological activity and therapeutic potential.
In the field of fine chemicals, this compound has also emerged. Fine chemicals are high-quality, high-purity special chemicals. This compound can be used as a key intermediate, and through clever chemical reactions, a wide variety of high-value-added fine chemicals can be derived. For example, in the fields of high-end coatings, special plastic additives, etc., it may give products excellent performance, such as better weather resistance, corrosion resistance, etc., thereby enhancing the market competitiveness of products.
Although its market prospects are bright, it also faces challenges. Optimization of the synthesis process is a top priority. To achieve large-scale production and reduce costs, it is necessary to seek more efficient and green synthesis paths. And product quality control is also crucial. It is necessary to ensure that each batch of products has stable quality in order to win the trust of the market. Despite difficulties and obstacles, the prospects are attractive. All parties will compete here. Over time, they will be able to shine in the market and inject new vitality into the pharmaceutical and chemical industries.