2 Butyl 3 Benzofuranyl 4 2 Diethylamino Ethoxy 3 5 Diiodophenyl Methanone

(2-Butyl-3-benzofuranyl) [4- [2- (diethylamino) ethoxy] -3,5-diiodophenyl] ketone, which is an organic compound. Its chemical properties are rich and unique.
First of all, the physical properties are usually solid. Due to the existence of various forces between molecules, it has a certain melting point and boiling point. However, the specific values vary depending on the preparation and purification conditions.
In terms of solubility, due to the polar and non-polar parts of the molecule, it has good solubility in organic solvents, such as common ethanol, acetone, dichloromethane, etc., which can be well dissolved; but it has poor solubility in water, because the overall hydrophobic part of the molecule accounts for a large proportion.
In terms of stability, it is relatively stable at room temperature and pressure without special chemical environment. However, in case of high temperature, strong oxidant or specific catalyst, the molecular structure will change. For example, at high temperature, the chemical bond between benzofuran ring and benzene ring may be cleaved; when strong oxidant acts, the iodine atom in the molecule may be oxidized, changing its chemical properties.
Its chemical activity comes from the functional groups contained. The carbonyl group (ketone part) is electrophilic and easily reacts with nucleophiles, such as with alcohols to generate ketals under acid catalysis; the nitrogen atom of the diethylaminoethoxy part has a lone pair of electrons, which has a certain nucleophilicity and can participate in nucleophilic substitution reactions. In addition, the hydrogen atom on the benzene ring and the benzofuran ring can undergo substitution reactions. Under specific conditions, such as under the catalysis of Lewis acid, other substituents can be introduced.
This compound has complex and diverse chemical properties and may have potential applications in organic synthesis, medicinal chemistry and other fields. It can be used as an intermediate to participate in the preparation of more complex compounds.

(2-Butyl-3-benzofuranyl) [4 - [2 - (diethylamino) ethoxy] - 3,5 - diiodophenyl] ketone, the use of this substance, in today's world, often involved in the field of medicinal chemistry.
The research and development of Guanfu Medicine, this compound may be a key raw material for the creation of new drugs. Because of its unique molecular structure, or with specific biological activities, it can interact with biological macromolecules in vivo. For example, in the study of neurological diseases, or by virtue of its structural properties, it targets neurotransmitter receptors and adjusts the transmission of neural signals in order to relieve or treat neurodegenerative diseases such as Alzheimer's disease and Parkinson's disease.
In the field of cardiovascular diseases, it may also have important uses. It can regulate the rhythm of the heart by affecting the function of ion channels, or act on vascular endothelial cells to improve the relaxation and contraction of blood vessels, thereby contributing to the development of drugs for diseases such as hypertension and arrhythmia.
Furthermore, in the exploration of cancer treatment, it may be used as a potential lead compound for anti-cancer drugs. It may interfere with the proliferation, invasion and metastasis of cancer cells, and induce cancer cell apoptosis by inhibiting specific signaling pathways, providing new ideas and directions for solving cancer problems.
In the process of chemical synthesis, this compound can also be used as a key intermediate. With its structural activity checking point, chemists can use a variety of organic synthesis methods to derive and modify it, expand the structural diversity of compounds, and then discover more new substances with excellent biological activities and pharmacological properties, which contribute to the development of medicinal chemistry.

To prepare (2-butyl-3-benzofuranyl) [4 - [2 - (diethylamino) ethoxy] - 3,5 - diiodophenyl] ketone, the method is as follows:
Take 2-butyl-3-benzofuranic acid first and react with appropriate reagents to convert it into the corresponding acid chloride. The preparation of this acid chloride should pay attention to the mild reaction conditions to prevent side reactions.
Then 4 - [2 - (diethylamino) ethoxy] - 3,5 - diiodobenzene is extracted, and it is reacted with the prepared acyl chloride in a suitable solvent with the help of a catalyst. This solvent is selected to have good solubility of the reactants and no interference with the reaction. The catalyst also needs to be precisely selected to promote the efficient progress of the reaction.
During the reaction process, the reaction process is closely monitored, and thin-layer chromatography can be used. After the reaction is completed, the product is purified through conventional post-processing steps such as extraction, washing, and drying. When extracting, choose a suitable extractant to ensure efficient separation of the product. Washing is designed to remove impurities, and drying makes the product pure.
Finally, the product was further purified by recrystallization or column chromatography to obtain high-purity (2-butyl-3-benzofuran) [4 - [2 - (diethylamino) ethoxy] - 3,5 -diiodophenyl] ketone. During the whole synthesis process, every step needs to be carefully operated, and attention should be paid to the control of reaction conditions to achieve the expected yield and purity.

(2-Butyl-3-benzofuranyl) [4- [2- (diethylamino) ethoxy] -3,5-diiodophenyl] ketone is a matter of safety and is extremely important. However, after searching the classics, it seems that there is no detailed information on the safety characteristics of this substance.
It is speculated that its chemical composition contains benzofuran, diiodophenyl and other parts. Benzofurans, some of which are biologically active or potentially toxic, are in living organisms or interfere with normal physiological processes. The halogenated benzene structure, that is, diiodophenyl, the halogen atom introduces or changes the polarity and reactivity of the compound, or increases its fat solubility, which is easy to accumulate in the living body and damage health.
From the theory of reactivity, the ketone group and nitrogen-containing and oxygen functional groups in its structure may be involved in chemical reactions under specific conditions. For example, ketone groups can participate in nucleophilic addition, in the complex biochemical environment in the body, or react with biological macromolecules such as proteins, nucleic acids and other activity check points, causing cell dysfunction and endangering the safety of the body.
As for environmental safety, if this substance is released in the environment, its complex structure may cause refractory degradation and long-term residue. And its potential toxicity, or acute and chronic toxic effects on organisms in the ecosystem, disrupts the ecological balance.
Although the above are all speculations, the safety of this substance requires rigorous scientific research, and its toxicological properties and environmental behavior can be determined by experiments to obtain accurate conclusions. To judge its impact on human health and the environment.

(2-Butyl-3-benzofuranyl) [4 - [2 - (diethylamino) ethoxy] -3,5 -diiodophenyl] ketone, which is on the market, its price range is difficult to determine. The price of this substance fluctuates greatly due to the difficulty of preparation, the difference in materials used, or the change in market demand.
According to the "Tiangong Kaiwu", the price of all kinds of materials varies according to time, place, and use. ( 2-Butyl-3-benzofuranyl) [4- [2- (diethylamino) ethoxy] -3,5-diiodophenyl] ketone, if its preparation requires concentrate and multiplication, it will be expensive; if its use is wide and urgent, the market demand is strong, and the price should be high. However, if it is easy to prepare and thin for users, the price may become more common.
In today's world, the price of chemical materials often changes with market supply and demand and the advance of science and technology. ( The price of 2-butyl-3-benzofuryl) [4 - [2 - (diethylamino) ethoxy] - 3,5 - diiodophenyl] ketone, or between tens of yuan and hundreds of yuan per gram, but this is only the number of years, the actual price must be carefully examined market conditions and asked the industry to be sure.