3-nitro-4-amino-5-iodopyridine

3-Nitro-4-amino-5-iodopyridine is one of the organic compounds. Its main uses are quite extensive.
In the field of medicinal chemistry, this compound is often a key intermediate. Due to its unique molecular structure, it can participate in many drug synthesis reactions. For example, for some drugs with specific biological activities, during the synthesis process, 3-nitro-4-amino-5-iodopyridine can introduce key structural fragments through ingenious chemical reactions, thereby imparting the desired pharmacological properties of the drug, such as antibacterial, antiviral, and antitumor effects.
In the field of materials science, it also has important applications. Or it can be used to prepare organic materials with special properties, such as optoelectronic materials. Due to the nitro, amino and iodine atoms contained in the structure, it can have a significant impact on the electron cloud distribution and optical properties of the material, so it is expected to prepare materials with unique optical absorption and emission properties, which will show potential in optoelectronic devices, such as Light Emitting Diode, solar cells and other fields.
In chemical research, 3-nitro-4-amino-5-iodine is often used as a model compound to help scientists explore the mechanism of organic reactions. Through detailed study of the reactions involving this compound, we can gain insight into the laws of chemical bond breaking and formation under various reaction conditions, and provide theoretical support and practical experience for the development of organic synthetic chemistry.
In summary, 3-nitro-4-amino-5-iodopyridine plays an indispensable role in many fields such as medicine, materials and chemical research, and is of great significance to promote the progress of related fields.

To prepare 3-nitro-4-amino-5-iodopyridine, there are two common methods.
First, pyridine is used as the starting material. Nitrify the pyridine first, so that the nitro group is introduced into the specific position of the pyridine ring. This step requires careful selection of nitrifying reagents and reaction conditions, such as using mixed acids (mixed nitric acid and sulfuric acid), controlling temperature and reaction time, etc., to achieve the desired regioselectivity to obtain nitro-containing pyridine derivatives. Subsequently, the nitro group is reduced and converted into an amino group. The commonly used reducing agents are iron/hydrochloric acid, tin/hydrochloric acid, etc. After this step, 4-amino-3-nitropyridine can be obtained. Finally, the iodization reaction is carried out on this basis, and the iodine elemental substance, potassium iodide and other reagents can be selected. In the presence of appropriate oxidants, such as hydrogen peroxide, the iodine atom is introduced into the designated position, so as to obtain the target product 3-nitro-4-amino-5-iodopyridine.
Second, a suitable pyridine derivative is used as the starting material. If the starting material already has some of the required functional groups, it can be converted into functional groups and the strategy of introducing new functional groups. For example, if the starting material contains a suitable transformable group, it is first converted into an amino or nitro group, and then the remaining groups are introduced in sequence. Halogen atoms can be introduced through halogenation reaction, and then the structure of the target molecule can be gradually constructed through a series of reactions such as nucleophilic substitution and oxidation reduction, and finally 3-nitro-4-amino-5-iodopyridine can be obtained. Each step of the reaction requires fine regulation of the reaction conditions, paying attention to the amount of reagents, temperature, pH and other factors to improve the reaction yield and selectivity.

3-Nitro-4-amino-5-iodopyridine is an organic compound with unique physical properties. Its properties are usually solid, because the molecular structure contains specific atoms and functional groups. The melting point of this compound also has its own characteristics. The melting point depends on the intermolecular force and lattice energy. The interaction of nitro, amino and iodine atoms in the molecule makes the melting point relatively high. However, the exact value needs to be determined by experiments. The boiling point is related to the intermolecular force and volatility. In view of the molecular polarity and relative molecular mass, its boiling point may be within a certain range, but the specific value also needs to be determined experimentally.
In terms of solubility, 3-nitro-4-amino-5-iodopyridine may have different solubility in organic solvents. Due to the presence of polar nitro and amino groups, it may have a certain solubility in polar organic solvents such as ethanol and acetone. Due to the principle of "similar miscibility", polar molecules and polar solvents are easy to interact. However, in non-polar organic solvents such as n-hexane, the solubility may be lower because the molecular polarity does not match the non-polar solvent.
In terms of color, the compound may have a specific color, which is due to the absorption and reflection characteristics of the molecular structure to light. Functional groups and conjugated systems in the molecule affect the electron transition, thus presenting the corresponding color, but the exact color still needs to be determined by actual observation. Density is also one of its physical properties. It depends on the molecular mass and the way of molecular packing, but the exact density value needs to be measured experimentally.
The physical properties of 3-nitro-4-amino-5-iodopyridine are determined by its molecular structure. In the fields of organic synthesis, medicinal chemistry, etc., its physical properties are crucial for the selection of reaction conditions, product separation and purification.

3 - nitro - 4 - amino - 5 - iodopyridine is an organic compound with unique chemical properties. Its properties are as follows:
1. ** Basic **: This compound contains an amino group (-NH ²). The nitrogen atom in the amino group has a lone pair of electrons and can accept protons, so it is alkaline to a certain extent. In an acidic environment, amino groups easily bind to protons to form positively charged ions. This property is beneficial for the construction of new chemical bonds and the separation and purification of products in organic synthesis reactions.
2. ** Nucleophilicity **: As an electron-rich group, amino groups are nucleophilic. Under suitable reaction conditions, they can attack electrophilic reagents and form new covalent bonds. For example, the nucleophilic substitution reaction can occur with halogenated hydrocarbons. The nitrogen atoms in the amino group attack the carbon atoms connected to the halogen in the halogenated hydrocarbons, and the halogen leaves to form new organic compounds. This reaction is extremely critical in the process of constructing complex organic molecular structures.
3. ** Oxidative **: The intra-molecular nitro group (-NO ²) is a strong electron-absorbing group and is oxidizing. Under specific reaction conditions, the nitro group can acquire electrons and be reduced, and its reduction products are rich and diverse. Depending on the reaction conditions and reducing agents, it can generate amino groups, oxidized azo groups, azo groups, etc., which provides an important way for the preparation of a variety of nitrogen-containing organic compounds.
4. ** Halogenation activity **: The 5 positions on the pyridine ring are already connected with iodine atoms. Because the iodine atom is an ortho-para-site group, and the electron cloud density distribution of the pyridine ring is affected by nitro and amino groups, the electron cloud density at a specific position of the pyridine ring changes, thereby affecting the halogenation activity and regioselectivity. Under suitable conditions, further halogenation reactions can occur at other active check points of the pyridine ring, resulting in the synthesis of halogenated pyridine derivatives with more complex structures.
5. ** Stability **: Since the pyridine ring is an aromatic system, it has certain stability. However, the 3-position nitro group and 5-position iodine atom are electron-withdrawing groups, and the 4-position amino group is the donor group, and these substituents have an impact on the electron cloud density and system stability of the pyridine ring. Overall, the compound can exist stably under normal conditions, but its structure will change under extreme conditions such as strong oxidizing agents, reducing agents or high temperatures.

3-Nitro-4-amino-5-iodopyridine, an important organic synthesis intermediate in the field of fine chemicals, is widely used in medicine, pesticides, materials and many other industries. However, its market price often fluctuates due to many factors such as quality, purity, suppliers, purchase volume and market supply and demand situation, and there is no fixed and uniform price range.
When it comes to high-quality reagent grade 3-nitro-4-amino-5-iodopyridine with a high purity of more than 98%, the price per gram may be in the hundreds of yuan in small scientific research procurement scenarios. This is because scientific reagents have strict quality requirements and fine production processes, so the cost is high.
If it is an industrial-grade product, its purity may be slightly lower, about 90% - 95%. If the purchase volume is large, such as the kilogram level or even the ton level, the unit price may be greatly reduced due to the scale effect. The price of kilograms may be around 1,000 yuan per ton or in the tens of thousands of yuan. However, suppliers in different regions will vary in price due to differences in raw material costs, transportation costs, market competition, etc.
If the market demand for 3-nitro-4-amino-5-iodopyridine is strong and the supply is relatively tight, the price will rise; conversely, if the market demand is weak and the supply is sufficient, the price may fall. To know the exact price range, you need to consult major chemical raw material suppliers and chemical trading platforms in real time to carefully observe the current market conditions in order to obtain accurate price information.