4 Nitro Isothiazole
Quinoline Thiophene Imidazole Thiazole
4-Nitro-isothiazole
Molecular Formula C3H2N2O2S
Molar Mass 130.126 g/mol
Appearance Solid (usually)
Physical State At Rt Solid
Melting Point Data needed
Boiling Point Data needed
Solubility In Water Low solubility
Solubility In Organic Solvents Soluble in some organic solvents (e.g., DMSO)
Density Data needed
Pka Data needed
Flash Point Data needed
Stability Can be stable under proper conditions, but sensitive to some reagents
FAQ

What are the main uses of 4-nitro-isothiazole?

4-Nitro-isothiazole is a class of organic compounds. It has a wide range of uses and is used in various fields.

In the field of medicinal chemistry, it is often an important intermediate. Pharmaceutical developers often use 4-nitro-isothiazole as a starting material and modify it through various chemical reactions to obtain compounds with specific biological activities. Such compounds may exhibit various pharmacological activities such as antibacterial, anti-inflammatory, and anti-tumor, providing a key cornerstone for the development of new drugs. For example, through clever chemical synthesis paths, its structure can be modified so that the resulting derivatives can precisely act on specific biological targets, helping to create new drugs.

In the field of materials science, 4-nitro-isothiazole also has its uses. Due to its special molecular structure, it can endow materials with different properties. Or it can be used to prepare functional polymer materials, by introducing specific functional groups to improve the electrical, optical or thermal properties of polymer materials. For example, in the preparation of some optoelectronic materials, the addition of 4-nitro-isothiazole may optimize the charge transfer performance of the material and improve its application efficiency in optoelectronic devices such as Light Emitting Diode and solar cells.

In addition, in the field of pesticide chemistry, 4-nitro-isothiazole also plays an important role. The compounds synthesized from it may have good insecticidal and bactericidal activities. Through rational molecular design, the synthesized pesticides can act efficiently on specific pests or pathogens, and have less impact on the environment, providing a more green and efficient means for agricultural pest control.

In summary, 4-nitro-isothiazole has important uses in medicine, materials, pesticides and other fields due to its unique structure, and has made great contributions to promoting scientific and technological progress in related fields.

What are the physical properties of 4-Nitro-isothiazole?

4-Nitroisothiazole is one of the organic compounds. Its physical properties are quite unique, and it is mostly solid at room temperature. Looking at its color, it is usually light yellow or almost white powder. This color characteristic may be related to the nitro group in the molecular structure. The presence of nitro groups causes the distribution of electron clouds to change, which in turn affects the absorption and reflection of light. Only then can this color appear.

When it comes to melting point, the melting point of 4-nitroisothiazole is in a specific range, between [X] ° C and [X] ° C. This melting point characteristic is determined by intermolecular forces, such as van der Waals forces, hydrogen bonds, etc. The arrangement of atoms and the characteristics of chemical bonds in the molecular structure determine the strength of the interaction between molecules, which affects the melting point.

As for solubility, 4-nitroisothiazole exhibits different solubility in common organic solvents. In polar organic solvents such as dimethyl sulfoxide (DMSO), N, N-dimethylformamide (DMF), its solubility is relatively high. This is because polar solvents and 4-nitroisothiazole molecules can form strong interactions, such as dipole-dipole interactions, which help the solute molecules to disperse in the solvent. However, in non-polar solvents such as n-hexane and benzene, its solubility is very low, and the interaction between non-polar solvents and polar 4-nitroisothiazole molecules is weak, making it difficult to overcome the force between solute molecules, making it difficult to dissolve.

Its density is also an important physical property, about [X] g/cm ³. The density depends on the mass of the molecule and the degree of molecular packing. The molecular structure of 4-nitroisothiazole and the type and quantity of constituent atoms together determine its density value. This density characteristic plays a significant role in many practical application scenarios, such as separation and purification.

What are the chemical properties of 4-Nitro-isothiazole?

4-Nitroisothiazole is one of the organic compounds. Its chemical properties are unique and valuable to explore.

Looking at its structure, the presence of nitro groups endows this substance with unique electronic effects. Nitro is a strong electron-absorbing group, which can reduce the electron cloud density on the isothiazole ring. This is a key factor affecting its chemical properties.

In terms of reactivity, 4-nitroisothiazole exhibits unique behavior in nucleophilic substitution reactions due to the change of electron cloud density. The carbon atoms on the isothiazole ring are more susceptible to attack by nucleophiles due to the electron-absorbing action of nitro groups. For example, when nucleophiles such as alcohols and amines meet them, or nucleophilic substitution can occur, a new group is introduced into the isothiazole ring.

Furthermore, 4-nitroisothiazole may have certain redox properties. Nitro groups can be reduced to other groups such as amino groups under specific conditions to obtain electrons. This property can be used in organic synthesis or as an important step in the construction of complex molecular structures.

In an acid-base environment, its chemical properties are also affected. The nitrogen atom in the isothiazole ring may have a certain alkalinity, but the presence of nitro groups may weaken this alkalinity. At the same time, under acidic conditions, reactions such as ring opening may be triggered, causing significant changes in its structure and properties.

In addition, the stability of 4-nitroisothiazole is also worthy of attention. Due to the strong electron-absorbing properties of nitro groups, the stability of isothiazole rings may be affected, and reactions such as decomposition may occur under special conditions such as high temperature and light.

In summary, the chemical properties of 4-nitroisothiazole are determined by its unique structure, which is reflected in nucleophilic substitution, oxidation and reduction, acid-base environment and stability, and is of great significance in the research and application of organic chemistry.

What is the synthesis method of 4-nitro-isothiazole?

The synthesis of 4-nitro-isothiazole is quite delicate. At the beginning of the method, suitable starting materials need to be used to skillfully transform into several steps.

Usually start with compounds containing sulfur, nitrogen and related functional groups. First, the sulfur-containing compound meets the nitrogen-containing reagent with a specific structure. Under appropriate reaction conditions, such as in a suitable solvent, control the temperature, pH, etc., to promote nucleophilic substitution or cyclization. This step of the reaction is like a craftsman carefully crafted to connect the atoms to each other and construct the basic framework of isothiazole.

Then, for the isothiazole structure that has been initially established, nitro groups need to be introduced. The method of introducing nitro groups is mostly nitrification reaction. Select suitable nitrifying reagents, such as mixed acids of nitric acid and sulfuric acid. Under careful control of the reaction conditions, the nitro group precisely replaces the hydrogen atom at a specific position on the isothiazole ring to obtain 4-nitro-isothiazole.

In this process, each step of the reaction needs to be carefully controlled. The choice of solvent depends on the rate and selectivity of the reaction. The temperature affects the process of the reaction and the purity of the product. The adjustment of pH is also crucial to the smooth progress of the reaction. Like ancient swords, the heat and materials need to be just right to create high-quality products. In this way, after many careful operations, 4-nitro-isothiazole can be obtained.

What is the price range of 4-Nitro-isothiazole in the market?

In today's world, it is not easy to know the price range of 4 - Nitro - isothiazole in the market. Although most of the "Tiangong Kaiwu" are the methods of creation at that time and the matters of hundreds of workers, it does not involve the price of this product, but I can make a little deduction according to common sense.

This 4 - Nitro - isothiazole may be a rare chemical substance, and its price should be influenced by many factors. The first one to bear the brunt is the difficulty of its preparation. If the preparation process is complicated, rare raw materials are required, and the equipment and skills are very demanding, its price will be high.

Furthermore, the state of market supply and demand is also the key. If there is a strong demand for this product in the fields of medicine, chemical industry, etc., but the supply is limited, the price will rise. On the contrary, if there is a lack of demand, the supply will exceed the demand, and the price will drop.

And its purity also affects the price. For high purity, the preparation is more difficult and the price is higher; for low purity, it is relatively cheap.

As for today's market, with common sense, if it is ordinary purity, the price per gram may be between tens and hundreds of yuan for general experimental research. If it is high purity, it is used in special fields such as high-end pharmaceutical research and development, and the price per gram may exceed 1,000 yuan, or even higher. It is difficult to say for sure, because the market changes, and the price changes at any time.