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What is the chemical structure of (2-butyl-3-benzofuranyl) (4-hydroxy-3,5-diiodophenyl) -methanone?
(2-Butyl-3-benzofuranyl) (4-hydroxy-3,5-diiodophenyl) methanone, which is an organic compound. To understand its chemical structure, let me explain it in detail.
Among its structure, the " (2-butyl-3-benzofuranyl) " part, benzofuran is a fused cyclic aromatic hydrocarbon structure, which is formed by fusing a furan ring with a benzene ring. Connecting butyl at position 2, butyl is an alkyl chain containing four carbon atoms, and its structure is -CH ² CH -2 CH ³ CH.
And the " (4-hydroxy-3,5-diiodophenyl) " part, the phenyl group is a benzene ring structure, and there is a hydroxyl group (-OH) at position 4, which gives the compound a certain polarity and reactivity. Positions 3 and 5 are respectively connected with iodine atoms, and the relative atomic weight of iodine atoms is relatively large, which affects the physical and chemical properties of the compound.
The two are connected by methylketonyl (-CO -), that is, carbonyl (C = O) carbon atoms are connected to benzofuranyl and diiodohydroxyphenyl, respectively, to form the overall chemical structure of (2-butyl-3-benzofuranyl) (4-hydroxy-3,5-diiodophenyl) methyl ketone. The interaction of various parts in this structure determines the unique physical and chemical properties of the compound, such as solubility, stability, reactivity, etc., which may have important applications and research value in organic synthesis, medicinal chemistry and other fields.
What are the main physical properties of (2-butyl-3-benzofuranyl) (4-hydroxy-3,5-diiodophenyl) -methanone?
(2-butyl-3-benzofuranyl) (4-hydroxy-3,5-diiodophenyl) -methanone has many physical properties. In terms of its state, it is often in a crystalline state, with regular crystalline morphology and fine texture. Viewed under an optical microscope, it can be seen that its crystal plane is flat and its crystal edges are clear, just like a naturally occurring delicate object.
When it comes to the melting point, it is about a specific temperature range, which is the key node of its transition from solid to liquid. When the external temperature gradually rises to the melting point, the material melts like ice in the spring sun, gradually turning from solid to liquid, and the state changes smoothly and orderly near the melting point.
In terms of solubility, it shows unique properties in organic solvents. For example, in some polar organic solvents, there is a certain solubility, just like salt dissolves in water, and the molecules are evenly dispersed to form a uniform and stable system; while in non-polar solvents, the solubility is very small, just like the incompatibility of oil and water, the molecules are difficult to disperse uniformly.
In addition, the color of this object may be white to yellowish, and the color is pure, giving people a sense of simplicity and elegance. Its density is also a specific value, which reflects the close arrangement of molecules inside the substance, just like the density of bricks in a building, which is related to its behavior in different environments. Such various physical properties are of great significance in chemical research and practical applications, laying the foundation for their subsequent development and utilization.
(2-butyl-3-benzofuranyl) In what fields is (4-hydroxy-3,5-diiodophenyl) -methanone used?
(2-butyl-3-benzofuran) (4-hydroxy-3,5-diiodophenyl) -methanone, this substance has applications in medicine, chemical industry and other fields.
In the field of medicine, it has potential medicinal value. Gein benzofuran and diiodophenyl structures can interact with specific targets in organisms. For example, benzofurans often have anti-inflammatory, antioxidant and anti-tumor activities. The 4-hydroxy-3,5-diiodophenyl structure may enhance its ability to bind to specific protein receptors, thereby regulating physiological processes. For example, in cancer treatment research, it can be developed as a targeted drug, which can precisely act on cancer cell-related targets, inhibit the proliferation and metastasis of cancer cells, and cause less damage to normal cells, which is expected to improve the therapeutic effect of cancer.
In the chemical field, it can be used as an intermediate in organic synthesis. Because of its unique chemical structure, it can participate in a variety of chemical reactions and build more complex organic molecules. Taking the synthesis of new polymer materials as an example, with the help of its reactivity, specific functional groups can be introduced to endow polymer materials with special properties, such as improving the optical and electrical properties of materials, or enhancing the mechanical properties and stability of materials, so as to meet different industrial needs, such as electronic devices, aerospace materials manufacturing and other fields.
And because it contains iodine atoms, it may have applications in flame retardancy of materials. Iodine can play a flame retardant role in combustion, introducing the substance into polymer materials, or improving the flame retardant properties of materials. It is widely used in construction, electronic appliances, and other industries with high fire safety requirements to reduce the risk of fire and ensure the safety of life and property.
(2-butyl-3-benzofuranyl) What are the preparation methods of (4-hydroxy-3,5-diiodophenyl) -methanone?
The preparation method of (2-butyl-3-benzofuran) (4-hydroxy-3,5-diiodophenyl) -methanone, although the ancient book "Tiangong Kaiwu" does not contain this material, there are many methods for preparing it. Now imitate its meaning, the above preparation method is as follows.
First take 2-butyl-3-benzofuran and find its source. When it is purchased from a suitable chemical reagent, its quality must be pure. Take 4-hydroxy-3,5-diiodobenzene and also seek its purity. Place the two in a clean reactor, the kettle must be dry and free of other disturbances.
Inject an appropriate amount of organic solvent into the kettle to make both soluble. The choice of organic solvent is related to the success or failure of the reaction. When using suitable ones, such as dichloromethane, N, N-dimethylformamide, etc., it depends on the nature of the reaction.
Add an appropriate catalyst to the kettle, the catalyst can promote the speed of the reaction and make it early. The dosage must be accurate, too much or too little is unfavorable. Then, the temperature in the kettle is controlled by a constant temperature device, and the temperature is high or low, depending on the needs of the reaction, either slowly rising or abruptly falling, so that the reaction is carried out in the best temperature range.
When the reaction is carried out, it is often stirred to make the matter mix evenly and the reaction is fast. After some time, measure it with an instrument, depending on whether the reaction is completed. If so, the product is separated by appropriate methods, such as distillation, extraction, and recrystallization.
When distilling, control the temperature to a certain extent to separate the product from others; for extraction, use a suitable extractant to extract the product from it; for recrystallization, choose a suitable solvent, dissolve the product, and then cool down to crystallize to obtain pure (2-butyl-3-benzofuran) (4-hydroxy-3,5-diiodophenyl) -methanone.
When preparing, pay attention to safety, avoid fire, poison, and rot, and abide by the rules of chemical experiments, so that you can get what you need.
How safe is (2-butyl-3-benzofuranyl) (4-hydroxy-3,5-diiodophenyl) -methanone?
(2-Butyl-3-benzofuranyl) (4-hydroxy-3,5-diiodophenyl) methanone, the safety of this substance is related to many aspects, let me tell you one by one.
Looking at its chemical structure, 2-butyl-3-benzofuran and 4-hydroxy-3,5-diiodophenyl are connected by methanone. However, this structure alone is difficult to determine the whole picture of its safety.
From a toxicological point of view, this substance contains diiodophenyl, iodine atoms have certain chemical activities. or trigger specific chemical reactions in living organisms, affecting the normal metabolism of cells. If inadvertently ingested, or interfere with the synthesis of human thyroid hormones, because iodine is a key raw material for thyroid hormones, excessive or abnormal iodine structural substances are involved, which can easily cause hormone imbalance and cause thyroid-related diseases.
When it comes to skin contact, the molecular structure of the substance may cause skin allergies. Its complex aromatic structure and halogen atoms may stimulate the skin's immune system, causing skin to appear redness, swelling, itching and other allergic symptoms.
As for environmental safety, when this substance enters the environment, its chemical stability or affects the degradation rate. Complex structures or microorganisms are difficult to decompose rapidly, and remain in soil and water, affecting the ecosystem. And its potential bioaccumulation cannot be ignored, or it is transmitted through the food chain and enriched in organisms, harming a wider range of biological populations.
However, rigorous experiments and studies are needed to accurately determine its safety. For example, cytotoxicity experiments are carried out to observe the effects on different cell lines; animal toxicology experiments are carried out to explore acute, subacute and chronic toxic effects. It is also necessary to consider its behavior under different environmental conditions in order to have a definite understanding of the safety of (2-butyl-3-benzofuran) (4-hydroxy-3,5-diiodophenyl) methanone.
