5 Iodo 2 3 Dihydro 1 Benzofuran

5-Iodine-2,3-dihydro-1-benzofuran, this is an organic compound. Its physical properties are usually solid, and accurate values such as melting boiling point need to be reviewed in professional literature.
In terms of chemical properties, iodine atoms endow their unique activities. As a good leaving group, iodine atoms can be replaced by many nucleophiles in nucleophilic substitution reactions, such as alkoxides, amines, etc., to generate products with different structures. For example, when reacted with alkoxides, corresponding ether compounds can be obtained; when reacted with amines, nitrogen-containing derivatives can be formed.
Furthermore, the double bonds in the structure of benzofurans can participate in the addition reaction. Under suitable conditions, it can be added with hydrogen halides, halogens, etc. If it reacts with bromine, the double bond can be added with bromine to form a dibromo substitute.
In addition, the compound is sensitive to external conditions such as light and heat. When exposed to light or heat, it may initiate decomposition or rearrangement reactions, resulting in molecular structure changes.
Due to its benzene ring structure, it has certain aromaticity and can participate in the unique electrophilic substitution reaction of aromatics, but the specific activity is affected by iodine atoms and other substituents. In terms of reactivity, it is necessary to comprehensively consider the electronic effects and steric resistance of each group in order to accurately predict the reaction process and products.

5-Iodo-2,3-dihydro-1-benzofuran is an organic compound with many common uses. In the field of medicinal chemistry, it is often a key intermediate for the creation of new drugs. Due to its unique structure, it can be chemically modified to derive compounds with various biological activities, such as antibacterial, anti-inflammatory, and anti-tumor effects. For example, through specific reactions, appropriate functional groups can be added, or their ability to bind to biological targets can be optimized, thereby enhancing the efficacy of drugs.
In the field of materials science, it also has applications. It can participate in the preparation of functional polymer materials, giving materials special optical or electrical properties. If it is introduced into the polymer system, it may improve the photoelectric conversion efficiency of the material, and make a name for itself in the fields of organic Light Emitting Diode (OLED) and solar cells. Because of its iodine atom and benzofuran structure, it may be able to adjust the electron cloud distribution of the material, affecting the charge transport and luminescence properties.
Furthermore, in organic synthetic chemistry, it is an important synthetic building block. Chemists can use it to participate in various organic reactions, such as nucleophilic substitution, coupling reactions, etc., to construct more complex organic molecular structures. By ingeniously designing the reaction path and using it as a starting material, the required target compounds can be gradually built, expanding the structural diversity of organic compounds, and contributing to the development of organic synthetic chemistry. In conclusion, 5-iodo-2,3-dihydro-1-benzofuran has important uses in many scientific fields, promoting research and development in related fields.

The synthesis of 5-iodine-2,3-dihydro-1-benzofuran is an important research in the field of organic synthesis. Its synthesis path often follows the following steps.
First, it can be started from a suitable phenolic compound. Using specific phenols as raw materials, iodine atoms are introduced into specific positions on the phenol ring through halogenation. This halogenation reaction requires careful selection of halogenating reagents, such as iodine elementals and appropriate catalyst combinations, and precise regulation of the reaction temperature, time and ratio of reactants. Too high or too low temperature, too long or too short time, and improper ratio can all cause deviations in reaction yield and selectivity.
Second, to construct the skeleton of benzofuran. It can be achieved by intramolecular cyclization reaction. The product of phenolic compounds halogenated is often used to interact with nucleophiles with appropriate activity under alkaline conditions. The strength of the alkaline environment needs to be carefully controlled, and the alkali that is too strong or too weak affects the reaction process. The activity of nucleophiles is also crucial. If the activity is too high or too low, it is not conducive to the effective construction of the benzofuran skeleton. In this step, the choice of reaction solvent cannot be ignored, and polar and non-polar solvents have a significant impact on the reaction rate and selectivity.
Furthermore, after the construction of the benzofuran skeleton, subsequent modification and purification of the product may be required. The purpose of modification is to achieve specific structural requirements, and the purification is to obtain high-purity 5-iodine-2,3-dihydro-1-benzofuran. The purification method often uses column chromatography, recrystallization and other means. Column chromatography needs to select suitable fixed phase and mobile phase, and recrystallization needs to select suitable solvent, so that the product can be effectively crystallized and precipitated to remove impurities and improve product purity.
Synthesis of 5-iodine-2,3-dihydro-1-benzofuran requires fine regulation of the conditions of each reaction step, careful selection of reagents, solvents, etc., in order to effectively achieve the synthesis of the target product and obtain higher yield and purity.

I look at your question, but I am inquiring about the market price of 5-iodo-2,3-dihydro-1-benzofuran. However, the price of this chemical is difficult to determine. The change in its price is influenced by various factors.
First, the price of raw materials is the main factor. If the price of all raw materials required for its synthesis is high and lacking, then the cost of 5-iodo-2,3-dihydro-1-benzofuran will increase, and its price will also increase. Otherwise, if the price of raw materials is abundant and low, the price may drop.
Second, the technique of production is also heavy. An efficient and refined production method can reduce costs and make prices cheaper. If the technique is clumsy and the consumption is too large, the price will be high.
Furthermore, the supply and demand situation in the market determines the price. If there are many people who want it, and there are few people who supply it, the price will rise; if the supply exceeds the demand, the price will fall.
There is also a distinction between brand and quality. A well-known factory focuses on quality control, and its product may be high in price. And if the quality is inferior, the price may be low.
And in different places, the price is also different at different times. In prosperous places, the price is high, and the price may be high; in remote places, the price may be low. During the peak sales season, the price rises; in the off-season, the price decreases.
To sum up, if you want to know the exact market conditions of 5-iodo-2,3-dihydro-1-benzofuran, you can obtain a more accurate price by carefully examining the raw materials, technology, supply and demand, brand and geographical conditions, or consulting chemical product suppliers.

5-Iodine-2,3-dihydro-1-benzofuran is an organic compound. When storing and transporting, it is necessary to pay attention to many matters.
The first word is storage. First, it should be placed in a cool and dry place. This compound is resistant to moisture and heat. If it is placed in a warm and humid place, it may cause deterioration. For example, when it is hot in the summer, if it is stored in a place without shade protection, or if the temperature is too high, it will cause a chemical reaction, which will damage its quality. Second, it needs to be sealed and stored. Because it may be sensitive to air, it is easy to interact with oxygen and other components when exposed to air, causing its chemical properties to change. Third, keep away from fire sources and oxidants. This compound may be flammable. In case of open flame, hot topic or oxidizer, or there is a risk of combustion or explosion, just like dry wood in case of fire, the disaster will take a moment.
Re-talk about transportation. When transporting, the packaging must be stable and tight. To prevent vibration and collision from causing package damage and compound leakage. At the same time, suitable transportation tools should also be selected to ensure that the transportation environment meets its storage requirements. Do not mix with flammable, explosive, strong oxidizer and other materials, otherwise, if fire and saltpeter are placed together, it is very easy to cause a disaster. And transportation personnel need professional training, familiar with the characteristics of the compound and emergency treatment methods, in case of emergencies, they can respond quickly to ensure the safety of transportation.