2 Butyl 1 Benzofuran 3 Yl 4 2 Diethylamino Ethoxy 3 5 Diiodophenyl Methanone
Iodobenzene

2 Butyl 1 Benzofuran 3 Yl 4 2 Diethylamino Ethoxy 3 5 Diiodophenyl Methanone

Fengxi Chemical

Specifications

HS Code

839804

Packing & Storage
Packing 100g of (2 - butyl - 1 - benzofuran - 3 - yl){4 - [2 - (diethylamino)ethoxy] - 3,5 - diiodophenyl}methanone in sealed container.
Storage (2-butyl-1-benzofuran-3-yl){4-[2-(diethylamino)ethoxy]-3,5-diiodophenyl}methanone should be stored in a cool, dry place away from direct sunlight. Keep it in a tightly sealed container to prevent exposure to air and moisture. Store in a well - ventilated area, away from heat sources and incompatible substances to ensure its stability and safety.
Shipping The chemical (2 - butyl - 1 - benzofuran - 3 - yl){4 - [2 - (diethylamino)ethoxy]-3,5 - diiodophenyl}methanone will be shipped in specialized, sealed containers, following strict chemical transport regulations to ensure safety during transit.
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General Information
Frequently Asked Questions
(2-butyl-1-benzofuran-3-yl) What is the chemical structure of {4- [2- (diethylamino) ethoxy] -3,5-diiodophenyl} methanone
The chemical structure of (2-butyl-1-benzofuran-3-yl) {4 - [2 - (diethylamino) ethoxy] -3,5 -diiodophenyl} methanone is one of the structures of organic compounds. Its structure can be analyzed as follows:
The first part of benzofuran is formed by fusing the benzene ring with the furan ring, and there is a butyl group connected at the 2 position. The butyl group is a straight-chain alkyl group containing four carbon atoms, with certain steric hindrance and hydrophobicity.
Furthermore, the one linked to the 3 position of benzofuran is a methyl ketone group. The methyl ketone group is connected to benzofuran at one end and to a benzene ring containing iodine and specific substituents at the other end.
The benzene ring is connected to an iodine atom at the 3rd and 5th positions. The iodine atom has a great influence on the physical and chemical properties of the molecule due to its large atomic radius and special electronegativity, such as increasing the polarity and weight of the molecule. The substituent connected to the 4th position is 4- [2- (diethylamino) ethoxy], in which the ethoxy group is connected to the benzene ring at one end and the diethylamino group at the other end. Diethylamino is basic and can participate in acid-base reactions. The connection of ethoxy groups increases the hydrophilicity and flexibility of the molecule.
These various structural parts are interconnected to form the overall chemical structure of (2-butyl-1-benzofuran-3-yl) {4 - [2 - (diethylamino) ethoxy] -3,5 -diiodophenyl} methanone, and the various parts interact to jointly determine the physical, chemical and biological activities of the compound.
(2-butyl-1-benzofuran-3-yl) What are the main uses of {4- [2- (diethylamino) ethoxy] -3,5-diiodophenyl} methanone
(2-Butyl-1-benzofuran-3-yl) {4 - [2 - (diethylamino) ethoxy] -3,5 -diiodophenyl} methanone, an organic compound. Its main uses are quite extensive, in the field of medicinal chemistry, or as a potential pharmaceutical active ingredient. In the process of many drug development, it is necessary to design and synthesize organic compounds with specific structures to find those with high affinity and biological activity for specific disease targets.
(2-butyl-1-benzofuran-3-yl) {4 - [2 - (diethylamino) ethoxy] -3,5 -diiodophenyl} methanone, or because of its unique chemical structure, can interact with specific receptors or enzymes in organisms, thereby regulating physiological processes and treating related diseases. In the initial stage of pharmacochemistry research, in vitro activity screening of newly synthesized compounds is often carried out to explore their effects on disease-related cell models or targets. If they show good activity, they are expected to become lead compounds, further optimize the structure, improve the efficacy, reduce toxicity and side effects.
In the field of materials science, such organic compounds may be used as special functional materials. Some organic compounds can be applied to organic Light Emitting Diodes (OLEDs), organic solar cells and other fields due to their unique physical and chemical properties such as light, electricity, and magnetism. (2-butyl-1-benzofuran-3-yl) {4 - [2 - (diethylamino) ethoxy] -3,5 -diiodophenyl} methanone, or its molecular structure endows it with special optical or electrical properties, which can be used as a key component of functional materials to improve material properties and device efficiency.
However, the specific use still depends on its detailed properties and related experimental studies. Before practical application, it is necessary to comprehensively explore its physical and chemical properties, biological activity, stability and many other aspects in order to give full play to its potential value.
(2-butyl-1-benzofuran-3-yl) What are the physical properties of {4- [2- (diethylamino) ethoxy] -3,5-diiodophenyl} methanone
(2-Butyl-1-benzofuran-3-yl) {4 - [2 - (diethylamino) ethoxy] -3,5 -diiodophenyl} methanone The physical properties of this substance are quite important and are related to many uses.
Looking at its appearance, it is often in a solid state, white or near-white powder, with a fine quality, like the first snow in winter, uniform and pure. This state is easy to store and use, with good stability. Under normal conditions, it can maintain its own shape for a long time, and is not disturbed by slight vibration and temperature changes.
Its melting point has a fixed number, about a specific temperature range. This temperature is just like the critical point for a substance to convert from solid to liquid. At this temperature, the substance gradually melts, like ice in the warm sun, from solid to flowing. The characteristics of the melting point can help to identify the authenticity, and are also a key guide for the production and processing to control the temperature.
In terms of solubility, it has a certain solubility in organic solvents such as ethanol and chloroform. This property is like a fish getting water, which allows the substance to integrate into a specific liquid environment, building a bridge for chemical reactions, and helping it to blend and react with other substances in the liquid phase system. In water, the solubility is very small, just like oil floating in water, clear and discernible, immiscible.
Density is also one of its physical characteristics. Although it is not intuitive, it is of great significance in practical applications. The value of density determines its position in the mixture and is related to the operation and design of separation, mixing and other processes.
In addition, this product may have a specific smell, but the strength and characteristics of the smell need to be distinguished by a fine sense of smell. It may have a slight aromatic aroma or a slight special smell. This odor feature may provide clues for its application in specific fields, such as the exploration of the edge of fragrance blending. Although it is not mainstream, it has potential.
The above physical properties are interrelated and together outline the physical profile of (2-butyl-1-benzofuran-3-yl) {4 - [2 - (diethylamino) ethoxy] -3,5 -diiodophenyl} methanone, paving the way for its research and application.
(2-butyl-1-benzofuran-3-yl) What is the synthesis method of {4- [2- (diethylamino) ethoxy] -3,5-diiodophenyl} methanone
The synthesis of (2-butyl-1-benzofuran-3-yl) {4 - [2 - (diethylamino) ethoxy] -3,5 -diiodophenyl} methyl ketone is an important matter in organic synthesis. The choice of the first raw material for the method. 2-butyl-1-benzofuran-3-formaldehyde is required, which can be obtained by introducing butyl through benzofuran derivatives with suitable alkylation reagents under suitable reaction conditions.
Furthermore, 4- [2- (diethylamino) ethoxy] -3,5-diiodobenzoic acid is also the key raw material. This can be started with 3,5-diiodophenol, first with halogenated ethanol, catalyzed by base, forming ether bonds, and then reacting with diethylamine to introduce diethylamino groups.
The core step of synthesis is carbonylation. In the presence of a suitable catalyst, such as a palladium-based catalyst, in a suitable solvent, carbon monoxide is introduced, and the temperature is raised to a suitable temperature, so that the carbonylation reaction of the two occurs to form the target product (2-butyl-1-benzofuran-3-yl) {4- [2- (diethylamino) ethoxy] -3,5-diiodophenyl} methanone. After the reaction is completed, the product can be purified by conventional separation and purification methods, such as column chromatography, recrystallization, etc., to obtain a pure target compound. After many practice optimization, this synthesis method can obtain ideal yield and purity, providing an effective way for the preparation of the compound.
(2-butyl-1-benzofuran-3-yl) {4- [2- (diethylamino) ethoxy] -3,5-diiodophenyl} methanone is a safety risk
(2-Butyl-1-benzofuran-3-yl) {4 - [2 - (diethylamino) ethoxy] -3,5 -diiodophenyl} methyl ketone is related to safety risks. I look at this chemical, its structure is complex, and it is formed by linking benzofuran with methyl ketone containing diethylaminoethoxy and diiodophenyl.
However, whether it is safe or not needs to be explored in many ways. First, in terms of chemical properties, atoms such as iodine and nitrogen may have certain reactivity. The existence of iodine atoms, or the molecule under specific conditions to participate in the substitution and other reactions, if the reaction is out of control, it is dangerous. Second, it involves its toxicity. Containing diethylamino structure, in some chemicals, such structures may have an impact on biological systems, such as interfering with the normal physiological function of cells, causing toxic effects, but the specific degree of toxicity must be confirmed by experiments. Third, consider its stability. Under different environmental factors such as temperature, light, pH, its structure may change, and if it decomposes to produce harmful products, it will also increase safety hazards.
To clarify its safety risks, it should be based on rigorous experiments to observe its chemical activity, toxicity and other characteristics, and not just based on structural assumptions. Therefore, based on existing information alone, it is difficult to determine the exact safety risk of this object, and more research and analysis will be required to determine whether it is safe in a specific scenario.