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What are the main uses of 2- (Ethylthio) -5-nitropyridine?
2 - (ethylthio) -5 -nitropyridine is also an organic compound. It has a wide range of uses and is useful in various fields such as medicine, pesticides, and material science.
In the field of medicine, it is an important intermediate for the synthesis of drugs. By combining with other compounds through specific chemical reactions, it can create drug molecules with specific biological activities. For example, it can participate in the synthesis of antibacterial and antiviral drugs. With its unique chemical structure, it can combine with specific targets of pathogens to block the metabolism or reproduction process of pathogens and achieve the purpose of treating diseases.
In the field of pesticides, its role should not be underestimated. It can be used as a key raw material for the synthesis of new pesticides, and pesticide products with high insecticidal, bactericidal or herbicidal properties can be developed. Due to its structural characteristics, it may selectively poison specific pests or weeds, and at the same time have a small impact on the environment, which meets the current green and environmentally friendly pesticide development needs.
In the field of materials science, 2- (ethylthio) -5-nitropyridine may be used to prepare special functional materials. Its chemical structure gives the material unique electrical, optical or thermal properties, and is used in electronic devices, optical materials, etc. For example, it may help to synthesize organic semiconductor materials with special electrical conductivity, providing a new way for miniaturization and high performance of electronic devices.
What are the physical properties of 2- (Ethylthio) -5-nitropyridine?
2-%28Ethylthio%29-5-nitropyridine, the Chinese name is often 2- (ethylthio) -5-nitropyridine. This substance has unique physical properties, allowing an old scholar to tell you in detail.
Looking at its properties, it is mostly yellow to light brown crystalline powder at room temperature. Its melting point is quite important, about 64-68 ℃. The characteristics of the melting point are the key basis for the identification and purification of this substance. When heated to this temperature, the solid phase will gradually melt into the liquid phase, which can be accurately measured by precision instruments.
Solubility is also an important property. 2- (ethylthio) -5-nitropyridine is slightly soluble in water, but it has better solubility in organic solvents such as ethanol, dichloromethane, and acetone. This property is derived from its molecular structure, which includes ethylthio and nitropyridine rings with certain hydrophobicity, making it difficult to dissolve in water with strong polarity; while the moderate polarity and intermolecular forces of organic solvents can interact with the substance to dissolve.
Its density is also fixed, although the exact value varies slightly due to the measurement conditions, roughly 1.2-1.3 g/cm ³. Density reflects the mass of a substance per unit volume. In chemical production, storage and transportation, this factor needs to be considered, and it is related to the actual operation of container selection and material ratio.
Furthermore, the vapor pressure of the substance is low. Vapor pressure characterizes the tendency of the substance to change from liquid or solid state to gaseous state. Low vapor pressure indicates that under normal temperature and pressure, the degree of volatilization to the gas phase is limited, relatively stable, not easy to be lost due to volatilization, and the storage conditions are correspondingly reduced.
The above physical properties are the cornerstones of the understanding and application of 2- (ethylthio) -5-nitropyridine, and play a crucial role in organic synthesis, drug development and other fields.
What is the chemical synthesis method of 2- (Ethylthio) -5-nitropyridine?
2-%28Ethylthio%29-5-nitropyridine is 2 - (ethylthio) -5 - nitropyridine, and its chemical synthesis method is as follows:
The starting material can be 2 - chloro - 5 - nitropyridine and ethanethiol salt. Place 2 - chloro - 5 - nitropyridine in a suitable reaction vessel and add an appropriate amount of organic solvent, such as N, N - dimethylformamide (DMF), to provide a good reaction environment. At the same time, dissolve ethanethiol salt in an appropriate amount of alkali solution. The commonly used bases can be potassium carbonate, sodium carbonate, etc. The alkali solution is slowly added dropwise to the reaction system containing 2-chloro-5-nitropyridine. During the dropwise addition process, attention should be paid to controlling the reaction temperature, generally maintained between room temperature and 50 ° C. This reaction is a nucleophilic substitution reaction. The sulfur atom in the ethanethiol salt acts as a nucleophilic reagent to attack the carbon atom connected to chlorine in 2-chloro-5-nitropyridine, and the chlorine atom leaves to form 2- (ethylthio) -5-nitropyridine.
After the reaction is completed, the reaction product needs to be separated and purified. An appropriate amount of water can be added to the reaction system to dissolve most of the inorganic salts, and then extracted with organic solvents such as dichloromethane and ethyl acetate. After the organic phase is dried with anhydrous sodium sulfate or magnesium sulfate, the organic solvent is removed by reduced pressure distillation to obtain the crude product. The crude product can be further purified by column chromatography. Silica gel is used as the stationary phase, and a suitable eluent is selected, such as the mixed solvent of petroleum ether and ethyl acetate. According to the difference in the partition coefficient between the product and the impurities in the stationary phase and the eluent, a pure 2 - (ethylthio) -5 -nitropyridine product is obtained.
Another synthesis idea can be started from 5-nitro-2-hydroxypyridine, which is reacted with ethyl thiochloride under alkaline conditions. The alkaline environment can be provided by organic bases such as triethylamine. The reaction is carried out in organic solvents such as dichloromethane. The reaction process is also nucleophilic substitution, and the hydroxyl group is replaced by ethyl thio group. The target product 2 - (ethyl thio) -5 - nitropyridine is obtained through similar separation and purification steps.
What are the precautions for 2- (Ethylthio) -5-nitropyridine in storage and transportation?
2 - (ethylthio) - 5 - nitropyridine is an organic compound. During storage and transportation, many matters need to be paid careful attention.
First talk about storage. Due to its nature or instability, the temperature and humidity of the primary storage environment. It should be placed in a cool, dry and well-ventilated place to prevent it from deteriorating due to excessive temperature and humidity. The temperature should be maintained within a specific range. Do not cause chemical reactions if it is too high, and if it is too low, it may cause its physical state to change, affecting the quality.
Furthermore, this compound may be toxic and corrosive to a certain extent, and must be stored in isolation from other substances. Do not mix with oxidizing agents, reducing agents, acids, alkalis, etc., to prevent interaction and cause dangerous reactions, such as explosion, generation of toxic gases, etc. Storage containers should also be carefully selected, and corrosion-resistant materials should be used, such as special glass bottles or plastic bottles, and ensure that they are well sealed to avoid leakage.
As for transportation, the same should not be taken lightly. Before transportation, the packaging must be tight to ensure that there is no risk of leakage during bumps. Transportation vehicles should be equipped with corresponding emergency treatment equipment and protective equipment to prevent accidents. Transportation personnel also need to be professionally trained to be familiar with the characteristics of this compound and emergency response methods. During transportation, follow the established route and stay away from densely populated areas and water sources to reduce risks.
In a word, the storage and transportation of 2- (ethylthio) -5-nitropyridine is related to safety and quality, and all links must be strictly controlled, and no sloppiness can be allowed.
What are the effects of 2- (Ethylthio) -5-nitropyridine on the environment and human health?
2-%28Ethylthio%29-5-nitropyridine is 2- (ethylthio) -5-nitropyridine. The impact of this substance on the environment and human health cannot be ignored.
If it is released into the environment, it may cause water pollution. Because of its specific chemical structure, it may be difficult to be rapidly decomposed by natural water purification processes. And may be toxic to aquatic organisms and interfere with their normal physiological functions. In soil, it may affect the balance of soil microbial communities, change the function of soil ecosystems, hinder the absorption of nutrients by plant roots, and cause plant growth to be hindered.
As for the impact on human health, after entering the human body through breathing, skin contact or accidental ingestion, it may damage human organs. The nitro and ethylthio groups they contain may interfere with the normal metabolic process of human cells. Or cause burden on detoxification and metabolic organs such as the liver and kidneys, causing damage to their functions. Long-term exposure to this substance may increase the risk of diseases, such as causing respiratory discomfort, skin allergies, and even potential carcinogenicity.
Therefore, when using and disposing of 2- (ethylthio) -5-nitropyridine, care should be taken, and proper measures must be taken to reduce its harm to the environment and human health, and to maintain ecological peace and human safety.