1-Ethoxy-2,3-difluoro-4-iodobenzene is also an organic compound. It is widely used in the field of medicinal chemistry and is often a key intermediate for the creation of new drugs. Due to its special molecular structure, fluorine, iodine and other halogen atoms coexist with ethoxy groups, endowing the compound with unique physical and chemical properties. It can participate in various chemical reactions and help build complex drug molecular structures. It has great potential in the development of antibacterial, antiviral and anti-cancer drugs.
In the field of materials science, or can be used to prepare materials with special photoelectric properties. The introduction of fluorine atoms can improve the stability, solubility and electron transport properties of materials; iodine atoms can adjust the optical absorption and emission characteristics of materials, so it is expected to be applied to organic Light Emitting Diode (OLED), organic solar cells and other optoelectronic devices to improve their performance and efficiency.
In addition, in the field of organic synthetic chemistry, this compound is an important intermediate. Through nucleophilic substitution, coupling and other reactions, it can derive many organic compounds with different structures, providing an effective way for the synthesis of novel organic materials and fine chemicals, and promoting the development of organic synthetic chemistry.

1-Ethoxy-2,3-difluoro-4-iodobenzene is also an organic compound. Its physical properties are particularly important and are related to many properties of this compound.
First of all, its appearance, under room temperature and pressure, or a colorless to light yellow liquid, the appearance is pure and free of impurities, and it looks like water, but it contains chemical mysteries.
As for the boiling point, it is about a certain temperature range, which is the key temperature for the substance to change from liquid to gas. The boiling point of 1-ethoxy-2,3-difluoro-4-iodobenzene is determined by the intermolecular force, so that when the substance is at a specific temperature, the molecular energy is sufficient to break free from the liquid phase and turn into a gaseous state.
Melting point is also an important physical property. When the temperature drops to a certain value, the substance solidifies from a liquid state to a solid state, and this temperature is the melting point. The melting point of 1-ethoxy-2,3-difluoro-4-iodobenzene depends on the molecular arrangement and interaction. In the solid state, the molecules are arranged in an orderly manner to maintain a stable structure.
Density cannot be ignored. Compared with common organic solvents, its density has a specific value. This value reflects the mass of the substance per unit volume, which is related to its distribution when it floats in solution and is mixed with other substances.
In terms of solubility, 1-ethoxy-2,3-difluoro-4-iodobenzene is soluble in some organic solvents, such as common ether, dichloromethane, etc. Due to the similar miscibility principle, its molecular structure is similar to that of organic solvents, so it can be miscible, but the solubility in water is very small, because its molecular polarity is different from that of water.
The physical properties of this compound are determined by its molecular structure. The presence of ethoxy, fluorine, and iodine atoms in the molecule affects the intermolecular forces, polarity, etc., which in turn determines its appearance, melting point, density, solubility, and other physical properties. It is of great significance in chemical research and practical applications.

The synthesis method of 1-ethoxy-2,3-difluoro-4-iodobenzene often follows several paths.
First, it can be started by a benzene derivative containing the corresponding substituent. For example, take the benzene containing ethoxy group first, and introduce fluorine atoms and iodine atoms through a halogenation reaction. In this process, the choice of halogenating reagents is very important. To conduct fluorine atoms, specific fluorination reagents can be selected, such as some metal fluorides and suitable catalysts. The introduction of iodine atoms can be achieved by a nucleophilic substitution reaction or an oxidized iodine substitution reaction. When nucleophilic substitution, a suitable iodine substitution reacts with a suitable leaving group on the benzene ring to form an iodine substitution product. The oxidized iodine generation uses an oxidizing agent to promote the electrophilic substitution of iodine ions to the benzene ring.
Furthermore, the construction of the benzene ring structure can be started. Using suitable small molecules as raw materials, the benzene ring is constructed through a multi-step reaction, and ethoxy, fluorine and iodine atoms are introduced at the same time. For example, some classical organic reactions, such as Fu-gram reaction, nucleophilic addition-elimination reaction, etc., are used to gradually splice molecular fragments. First, ethoxy is introduced by Williamson ether synthesis with appropriate halogenated hydrocarbons and phenolic compounds under base catalysis. After that, fluorine and iodine atoms are introduced in sequence during the construction of the benzene ring or after the benzene ring is formed. The control of reaction conditions is related to the purity and yield
Or, the reaction is catalyzed by transition metals. Transition metal catalysts can effectively promote the coupling reaction of halogenated aromatics. For example, the reaction catalyzed by palladium allows the coupling of halogenated aromatics containing ethoxy and fluorine atoms with iodine reagents to achieve precise access of iodine atoms. This approach requires attention to the activity of the catalyst, the selection of ligands, and the influence of the reaction solvent and base to optimize the reaction and obtain the target product 1-ethoxy-2,3-difluoro-4-iodobenzene.

1-Ethoxy-2,3-difluoro-4-iodobenzene is also an organic compound. During storage and transportation, many matters must be paid attention to.
First, the storage place must be cool and dry. This compound is afraid of moisture. If it is in a humid place, it is easy to cause hydrolysis and damage its purity and quality. Therefore, it should be placed in a sealed container to avoid contact with water vapor.
Second, temperature is also critical. Excessive temperature can cause its chemical properties to be unstable, or reactions such as biodecomposition and polymerization. Therefore, the storage temperature should be controlled within a specific range, usually at a low temperature, but it should not be too low to avoid solidification of the substance and affect the use.
Furthermore, when transporting, it is necessary to ensure that the packaging is intact. Because of its certain chemical activity, if the packaging is damaged, leaks out, or reacts with surrounding substances, it will not only endanger the safety of transportation, but also pollute the environment. And during transportation, vibration and collision must be prevented to avoid damage to the packaging.
Also, this compound may be toxic and irritating to a certain extent. Those who store and transport must wear suitable protective equipment, such as gloves, goggles, etc., to prevent contact and injury. In case of accidental contact, rinse with plenty of water as soon as possible and seek medical attention according to the injury.
Again, storage and transportation places should be kept away from fire sources, heat sources and strong oxidants. This compound is flammable, and in case of open flames, hot topics or strong oxidants, it is easy to cause the risk of combustion or even explosion.
In general, in the storage and transportation of 1-ethoxy-2,3-difluoro-4-iodobenzene, moisture prevention, temperature control, packaging protection, personnel protection, and avoidance of dangerous substances are all essential, and all are indispensable, so as to ensure its safety and not damage its properties.

I do not know the market price of 1-ethoxy-2,3-difluoro-4-iodobenzene. The market price of this compound often varies due to multiple factors, such as raw material cost, difficulty in synthesis, market supply and demand, etc.
The cost of raw materials has a significant impact on its price. If the starting material required to prepare 1-ethoxy-2,3-difluoro-4-iodobenzene is scarce or expensive, the cost of this compound must be high, and the market price will also increase accordingly. For example, if the required special fluoride or iodide is expensive, it will significantly increase the overall cost.
The difficulty of synthesis is also key. If its synthesis requires complex steps, special reaction conditions or high-purity reagents, the production cost will be greatly increased. Or the use of rare catalysts, reactions at extreme temperatures or pressures will increase costs, which will affect market prices.
Furthermore, market supply and demand determine prices. If there is strong demand for 1-ethoxy-2,3-difluoro-4-iodobenzene in many industries, such as pharmacies used to synthesize specific drugs, and supply is limited, prices tend to rise. Conversely, if demand is low, and there are many manufacturers and sufficient supply, prices may fall.
To know the exact market price, you can consult chemical product suppliers, check chemical trading platforms, or consult industry experts, who can provide more accurate price information based on current market trends.