3 Nitro 5 Fluoro Iodo Benzene

3-Nitro-5-fluoro-iodobenzene is an important intermediate in organic synthesis and has key uses in many fields.
First, in the field of medicinal chemistry, this compound can be used as a building block for various drug molecules. Due to the nitro group, fluorine atom and iodine atom contained in its structure, it can endow drugs with specific biological activities and pharmacokinetic properties. Nitro groups can affect the electron cloud distribution of molecules and change their interaction with biological targets; fluorine atoms can enhance the lipid solubility of drug molecules, improve their transmembrane ability, and increase the metabolic stability of molecules due to their unique atomic radius and electronegativity; iodine atoms can be used as radioactive markers in the preparation of radiopharmaceuticals in some cases to assist in the diagnosis and treatment of diseases. In the development of many new anti-cancer, anti-infection and neurological drugs, 3-nitro-5-fluoro-iodobenzene is used as the starting material, and complex molecular structures with specific activities are constructed through multi-step reactions.
Second, in the field of materials science, 3-nitro-5-fluoro-iodobenzene can be used to prepare functional materials. For example, in the synthesis of organic optoelectronic materials, the introduction of this compound can adjust the electron transport properties and optical properties of the material. By reasonably designing and connecting with other conjugated structural units, organic semiconductor materials with specific emission wavelengths or high carrier mobility can be prepared, which can be used in optoelectronic devices such as organic Light Emitting Diodes (OLEDs) and organic solar cells. Its unique combination of functional groups can regulate the interaction and accumulation mode between molecules, thereby optimizing the overall properties of the material.
Furthermore, in the study of organic synthesis methodologies, 3-nitro-5-fluoro-iodobenzene is often used as a substrate to explore new chemical reaction pathways and synthesis strategies. Due to the existence of different functional groups in its molecules, diverse reactions can be carried out, such as nucleophilic substitution reactions, metal-catalyzed coupling reactions, etc. Researchers have developed more efficient and green organic synthesis methods by trying different reaction conditions and catalysts to achieve selective conversion of its functional groups, providing new approaches and ideas for the construction of complex organic molecules.
To sum up, 3-nitro-5-fluoro-iodobenzene, with its unique structural characteristics, plays an indispensable role in the fields of drug development, material preparation, and organic synthesis methodology, and promotes the continuous progress and development of related science and technology.

The synthesis of 3-nitro-5-fluoro-iodobenzene involves several processes. One is the halogenation reaction. First, take the appropriate aromatic compound as the starting material, such as 3-nitro-5-fluorobenzene, and make it with the iodine source, such as iodine elemental substance ($I_2 $), under specific reaction conditions. In this case, the help of catalysts may be required, such as commonly used copper salt catalysts, such as cuprous iodide ($CuI $). And with appropriate ligands, such as 1,10-phenanthroline, it can promote the selective substitution of iodine atoms to benzene rings, and finally obtain the target product 3-nitro-5-fluoro-iodobenzene. This reaction environment often needs to be carried out in organic solvents, such as N, N-dimethylformamide (DMF), and the temperature, reaction time and other factors are also required to be precisely regulated in order to improve the yield.
Furthermore, it may be achieved by nucleophilic substitution reaction. First, a 3-nitro-5-fluorobenzene derivative containing a suitable leaving group, such as 3-nitro-5-fluorobenzene halide (in which the halogen atom can be chlorine, bromine, etc.), is prepared. Then, the derivative is reacted with iodide salts, such as potassium iodide ($KI $), in a suitable solvent, such as acetone, under heating conditions. The halogen atom leaves, and the iodine ion takes its place, thus forming 3-nitro-5-fluoro-iodobenzene. During the reaction, the polarity of the solvent, the proportion of the reactants, and the reaction temperature all have a significant impact on the reaction process and product yield, and need to be carefully considered.
Another strategy for constructing benzene rings through multi-step reactions is to. The chain-like compounds containing fluorine, nitro and other functional groups were first prepared by organic synthesis, and then the benzene ring structure was constructed by cyclization reaction. In this process, iodine atoms were gradually introduced to obtain 3-nitro-5-fluoro-iodobenzene. Although this path is complicated, under specific circumstances, it may have unique advantages and can be selected according to factors such as the availability of starting materials and the difficulty of controlling the reaction conditions.

3-Nitro-5-fluoro-iodobenzene is also an organic compound. Its physical properties are particularly important, related to chemical and scientific research.
When it comes to appearance, at room temperature, it is mostly solid, colored or light yellow, with a crystalline state, uniform and moist. When storing and transporting this state, attention should be paid to protection against damage or qualitative change.
Melting point, the characteristics of organic compounds are also marked. The melting point of 3-nitro-5-fluoro-iodobenzene is specific, and accurate values can be obtained by measurement. This value helps to distinguish the purity of substances and is also a key indicator for temperature control in chemical processes. When the temperature rises to the melting point, the substance melts into a liquid, and the shape changes. The intermolecular force is also affected by temperature.
The boiling point is also an important physical property. When the boiling point is reached, the liquid 3-nitro-5-fluoro-iodobenzene will melt into a gaseous state. The determination of boiling point is indispensable in the separation and purification process. With the difference in boiling point, the substance can be separated from other substances to obtain a pure product.
The solubility is related to its dispersion in various solvents. This compound may have a certain solubility in organic solvents such as ethanol and ether. However, in water, due to the difference in molecular polarity and water, the solubility may be low. The difference in solubility can be used as a guide in the selection of media and product separation in chemical reactions.
The density is the mass of the substance per unit volume. The density of 3-nitro-5-fluoro-iodobenzene is an important consideration in chemical design, pipeline transportation, container loading and other links. With a given density, the space occupied by the material can be known, and its quality can also be estimated, which is of great significance in production planning.
And its smell, or a special smell, although not pungent and unpleasant, it is still necessary to be cautious when operating. Because of its smell or implied toxicity, ventilation protection is essential.
In summary, the physical properties of 3-nitro-5-fluoro-iodobenzene are fundamental and critical elements in the fields of chemical production and scientific research. Only by understanding their properties can we make good use of them.

3-Nitro-5-fluoro-iodobenzene is also an organic compound. It has various chemical properties, which are related to the reactivity and stability, and are quite important in the field of organic synthesis.
In terms of its chemical activity, both halogen atoms (fluorine, iodine) and nitro groups are affected. Fluorine atoms have strong electronegativity, which can cause the density of the electron cloud of the benzene ring to change, so that the density of the adjacent and para-potential electron clouds decreases, and the meta-potential is relatively higher. Therefore, during the electrophilic substitution reaction, the new group mostly enters the meta-potential. Although the electronegativity of the iodine atom is weaker than that of fluorine, its atomic radius is large and it has a certain degree of polarization. It also affects the distribution of the electron cloud of the benzene ring, and
The nitro group is a strong electron-absorbing group, which greatly reduces the electron cloud density of the benzene ring, causing the activity of the electrophilic substitution reaction of the benzene ring to decrease, while the activity of the nucleophilic substitution reaction to increase. Due to the electron-absorbing conjugation effect and induction effect of the nitro group, the nucleophilic substitution reaction intermediate can be stabilized, and the reaction can proceed.
In terms of stability, 3-nitro-5-fluoro-iodobenzene is relatively stable under normal conditions. When exposed to high temperature, strong oxidants or reducing agents, its structure may change. In case of strong reducing agents, nitro groups can be reduced to amino groups; in case of strong oxidants, benzene rings may be oxidized
In terms of solubility, because it is an organic compound, it has a certain solubility in organic solvents such as dichloromethane, chloroform, ether, etc., but poor solubility in water, which is caused by its non-polar molecular structure.
In organic synthesis, 3-nitro-5-fluoro-iodobenzene is an important intermediate. Various functional groups can be introduced through reactions such as nucleophilic substitution and electrophilic substitution to produce a variety of organic compounds, which are widely used in drug synthesis, materials science and other fields.

There is a price range of 3-nitro-5-fluoro-iodo-benzene in the market. However, if you want to push the price range, you can measure it according to common sense and the price of related substances.
The price of a chemical is related to many factors. One is the difficulty of preparation. If the preparation of this product requires complicated steps, harsh conditions, and rare raw materials, its price must be high. The preparation process may involve multiple steps of reaction, and the yield and purity of each step need to be strictly controlled. If there is a slight difference, the cost will increase significantly. The second is the amount of demand. If there is a high demand for this product in scientific research, industrial production and other fields, the price may be driven by it; if there is little demand, the merchant may spread the cost due to limited production, and the price is not low. The third is the price of raw materials. If the price of nitro, fluorine, iodine and other related raw materials required for preparation is high, the price of this compound is also difficult to be low.
In terms of benzene series compounds containing fluorine, iodine and nitro groups, if it is an ordinary scientific research grade purity, the price per gram may be between tens of yuan and hundreds of yuan. If the purity requirements are extremely high, such as for high-end fields such as pharmaceutical research and development, the price per gram or more than 1,000 yuan. However, this is only a guess, and the actual price may vary greatly due to changes in market supply and demand, differences in manufacturers, and geographical differences. To know the exact price, please consult the chemical reagent supplier in detail to obtain an accurate number.