Linshang Chemical
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1,2,4,5-Tetrachloro-3-Nitrobenzene
Linshang Chemical
|
HS Code |
848235 |
| Chemical Formula | C6HCl4NO2 |
| Molecular Weight | 266.89 |
| Appearance | Yellow solid |
| Odor | Unpleasant |
| Density | 1.75 g/cm³ |
| Melting Point | 87 - 90 °C |
| Boiling Point | 315.5 °C |
| Solubility In Water | Very low |
| Solubility In Organic Solvents | Soluble in benzene, toluene |
| Vapor Pressure | Very low |
| Stability | Stable under normal conditions |
As an accredited 1,2,4,5-Tetrachloro-3-Nitrobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 500g of 1,2,4,5 - tetrachloro - 3 - nitrobenzene packaged in a sealed chemical - grade bottle. |
| Storage | 1,2,4,5 - Tetrachloro - 3 - nitrobenzene should be stored in a cool, dry, well - ventilated area away from sources of heat, ignition, and incompatible substances. Keep it in a tightly closed container, preferably made of corrosion - resistant materials. Store it separately from oxidizing agents, reducing agents, and reactive chemicals to prevent potential reactions. |
| Shipping | 1,2,4,5 - Tetrachloro - 3 - nitrobenzene is a hazardous chemical. Shipping requires proper packaging in accordance with regulations, like using UN - approved containers, and strict documentation to ensure safe transportation. |
Competitive 1,2,4,5-Tetrachloro-3-Nitrobenzene prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615365006308 or mail to info@alchemist-chem.com.
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Tel: +8615365006308
Email: info@alchemist-chem.com
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As a leading 1,2,4,5-Tetrachloro-3-Nitrobenzene supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.
What are the chemical properties of 1,2,4,5-tetrachloro-3-nitrobenzene?
The chemical properties of 1% 2C2% 2C4% 2C5-tetrahydro-3-carbonyl indole are the object of much attention in organic chemistry. This compound has a unique structure and active reactivity.
In terms of physical properties, it is mostly crystalline solid at room temperature, and has a certain melting point and boiling point due to intermolecular forces. And according to changes in the surrounding environment, the solubility is also different. It often shows good solubility in organic solvents such as ethanol and ether, which provides convenience for its synthesis and separation operations.
In terms of chemical properties, carbonyl is the active check point. Due to its electron-absorbing properties, carbonyl carbons are positively electrically charged and vulnerable to attack by nucleophiles. Nucleophiles such as alcohols and amines can react with carbonyl groups to generate corresponding acetals, acetals, amines and other derivatives. This reaction is often an important means to construct complex molecular structures in the field of organic synthesis.
Furthermore, the existence of the indole ring endows the compound with unique aromaticity and electron cloud distribution. The carbon atoms on the indole ring can undergo electrophilic substitution reactions, and the selectivity of the reaction check point is related to the electronic effect of the substituents on the ring. The electrophilic substitution occurs in high electron cloud density locations, such as the 3-position or 5-position of the indole ring, when there is a supply group on the ring.
In addition, although the tetrahydro moiety slightly reduces the rigidity of the indole ring, it also affects the stability and reactivity of the molecule. Under appropriate oxidation or reduction conditions, the tetrahydro moiety can undergo reactions such as ring opening or hydrogenation, and then derive products with different structures.
Overall, 1% 2C2% 2C4% 2C5-tetrahydro-3-carbonyl indoles have rich and diverse chemical properties, and have important application value and research potential in many fields such as organic synthesis and medicinal chemistry.
In terms of physical properties, it is mostly crystalline solid at room temperature, and has a certain melting point and boiling point due to intermolecular forces. And according to changes in the surrounding environment, the solubility is also different. It often shows good solubility in organic solvents such as ethanol and ether, which provides convenience for its synthesis and separation operations.
In terms of chemical properties, carbonyl is the active check point. Due to its electron-absorbing properties, carbonyl carbons are positively electrically charged and vulnerable to attack by nucleophiles. Nucleophiles such as alcohols and amines can react with carbonyl groups to generate corresponding acetals, acetals, amines and other derivatives. This reaction is often an important means to construct complex molecular structures in the field of organic synthesis.
Furthermore, the existence of the indole ring endows the compound with unique aromaticity and electron cloud distribution. The carbon atoms on the indole ring can undergo electrophilic substitution reactions, and the selectivity of the reaction check point is related to the electronic effect of the substituents on the ring. The electrophilic substitution occurs in high electron cloud density locations, such as the 3-position or 5-position of the indole ring, when there is a supply group on the ring.
In addition, although the tetrahydro moiety slightly reduces the rigidity of the indole ring, it also affects the stability and reactivity of the molecule. Under appropriate oxidation or reduction conditions, the tetrahydro moiety can undergo reactions such as ring opening or hydrogenation, and then derive products with different structures.
Overall, 1% 2C2% 2C4% 2C5-tetrahydro-3-carbonyl indoles have rich and diverse chemical properties, and have important application value and research potential in many fields such as organic synthesis and medicinal chemistry.
What are the hazards of 1,2,4,5-tetrachloro-3-nitrobenzene in the environment?
1% 2C2% 2C4% 2C5 refers to tetrahydro-3-furanyl sulfur, which has many hazards in the environment. If this substance is released into the atmosphere, it will undergo complex photochemical reactions with other chemical substances in the atmosphere. Its reaction products or aerosol components affect the visibility of the atmosphere, make the air turbid, affect the transmission of sunlight, interfere with the normal photoperiod of organisms, and affect the growth, reproduction and other life activities of animals and plants.
In the aquatic environment, it poses a serious threat to aquatic organisms. Aquatic organisms are exposed to water bodies containing this substance for a long time, or their physiological functions are damaged. For example, the nervous system of fish may be disturbed, affecting their swimming, predation, avoidance of natural enemies, etc.; to plankton, or damage their cell structure and metabolic process, affecting the energy transfer and material circulation of the entire aquatic ecosystem. Moreover, through the food chain, this substance can be enriched in organisms. After ingested by small aquatic organisms, it is preyed on by large organisms, and the concentration continues to accumulate. Humans eat contaminated aquatic organisms, and harmful substances can enter the human body, endanger health, or cause diseases of the nervous system and immune system.
If this substance exists in the soil, it will affect the activity of soil microorganisms. Soil microorganisms are essential for soil nutrient transformation and decomposition of organic matter. If their activity is suppressed, it will disrupt soil ecological balance, affect plant root absorption of nutrients, hinder plant growth and development, and even cause plant death, affecting the stability and productivity of the entire terrestrial ecosystem.
In short, 1% 2C2% 2C4% 2C5-tetrahydro-3-furanyl sulfur poses significant hazards to the atmosphere, water, soil ecosystems and biological health in the environment, and its use and discharge need to be strictly controlled to protect the environment and biological safety.
In the aquatic environment, it poses a serious threat to aquatic organisms. Aquatic organisms are exposed to water bodies containing this substance for a long time, or their physiological functions are damaged. For example, the nervous system of fish may be disturbed, affecting their swimming, predation, avoidance of natural enemies, etc.; to plankton, or damage their cell structure and metabolic process, affecting the energy transfer and material circulation of the entire aquatic ecosystem. Moreover, through the food chain, this substance can be enriched in organisms. After ingested by small aquatic organisms, it is preyed on by large organisms, and the concentration continues to accumulate. Humans eat contaminated aquatic organisms, and harmful substances can enter the human body, endanger health, or cause diseases of the nervous system and immune system.
If this substance exists in the soil, it will affect the activity of soil microorganisms. Soil microorganisms are essential for soil nutrient transformation and decomposition of organic matter. If their activity is suppressed, it will disrupt soil ecological balance, affect plant root absorption of nutrients, hinder plant growth and development, and even cause plant death, affecting the stability and productivity of the entire terrestrial ecosystem.
In short, 1% 2C2% 2C4% 2C5-tetrahydro-3-furanyl sulfur poses significant hazards to the atmosphere, water, soil ecosystems and biological health in the environment, and its use and discharge need to be strictly controlled to protect the environment and biological safety.
What are the preparation methods of 1,2,4,5-tetrachloro-3-nitrobenzene?
The preparation method of 1% 2C2% 2C4% 2C5-tetrahydro-3-carbonyl indole is an important matter for the synthesis of these compounds. In the context of "Tiangong Kaiwu", although this specific organic synthesis method is not detailed, it can be deduced by traditional chemical process thinking.
The preparation of this product in the past may require exquisite selection and ratio of raw materials. First, choose the material as the essence, and you can find natural materials or easily available chemical raw materials rich in related functional groups. If you start with natural materials, such as some plant extracts with specific structures, they are refined and purified many times to obtain usable basic materials.
Second, the control of reaction conditions is extremely critical. In ancient times, heat was used to adjust the reaction temperature. Heating up can promote the reaction rate, but if it is too high, it may cause frequent side reactions. If you use a kettle as a container and char as a heat source, slowly heat up to a moderate level, so that the reactants can fully function in it.
Third, the reaction medium should not be underestimated. Water or some organic solvents can be used as the reaction medium. Different media affect the direction, rate and product purity of the reaction. If you choose an organic solvent, check its solubility, volatility and safety.
In addition, the separation and purification steps are also indispensable. The product is initially formed and often mixed with impurities. By distillation, the target product can be separated according to the difference in the boiling point of each substance. Or use recrystallization to select a suitable solvent to crystallize and precipitate the product in it for the purpose of purification. Although the ancient method may be different from the modern synthesis method, the basic chemical principles and operating thinking may have something in common, all of which are for the efficient and high-purity preparation of 1% 2C2% 2C4% 2C5-tetrahydro-3-carbonyl indole, an important compound.
The preparation of this product in the past may require exquisite selection and ratio of raw materials. First, choose the material as the essence, and you can find natural materials or easily available chemical raw materials rich in related functional groups. If you start with natural materials, such as some plant extracts with specific structures, they are refined and purified many times to obtain usable basic materials.
Second, the control of reaction conditions is extremely critical. In ancient times, heat was used to adjust the reaction temperature. Heating up can promote the reaction rate, but if it is too high, it may cause frequent side reactions. If you use a kettle as a container and char as a heat source, slowly heat up to a moderate level, so that the reactants can fully function in it.
Third, the reaction medium should not be underestimated. Water or some organic solvents can be used as the reaction medium. Different media affect the direction, rate and product purity of the reaction. If you choose an organic solvent, check its solubility, volatility and safety.
In addition, the separation and purification steps are also indispensable. The product is initially formed and often mixed with impurities. By distillation, the target product can be separated according to the difference in the boiling point of each substance. Or use recrystallization to select a suitable solvent to crystallize and precipitate the product in it for the purpose of purification. Although the ancient method may be different from the modern synthesis method, the basic chemical principles and operating thinking may have something in common, all of which are for the efficient and high-purity preparation of 1% 2C2% 2C4% 2C5-tetrahydro-3-carbonyl indole, an important compound.
What are the uses of 1,2,4,5-tetrachloro-3-nitrobenzene?
1% 2C2% 2C4% 2C5-tetrahydro-3-carbonyl indole, this substance is widely used in the fields of medicine and chemical industry.
In pharmaceutical research and development, one of them can be used as a key intermediate to synthesize a variety of biologically active compounds. Due to the special chemical structure of this substance, it is possible to interact with specific targets in organisms. For example, some studies have shown that derivatives based on it may inhibit or activate enzymes related to certain diseases, paving the way for the development of new therapeutic drugs, such as innovative drug development for specific cancers and neurological diseases. Second, in the optimization of pharmaceutical chemistry, it can be used as a starting point for structural modification. By modifying and modifying its chemical structure, such as introducing different substituents at specific locations, chemists can effectively adjust the physical and chemical properties of drug molecules, such as solubility, stability, and affinity with targets, thereby improving drug efficacy and reducing toxic and side effects.
In the chemical field, first of all, in organic synthetic chemistry, it is used as a multi-functional synthetic building block. With its unique structure, it can participate in various types of chemical reactions, such as nucleophilic substitution, electrophilic addition, etc., and then construct complex and diverse organic compounds, providing key raw materials for the synthesis of new materials and fine chemicals. Secondly, in the field of materials science, some compounds derived from 1% 2C2% 2C4% 2C5-tetrahydro-3-carbonyl indoles may exhibit unique optical and electrical properties, which are expected to be applied to the preparation of photovoltaic materials, such as organic Light Emitting Diodes (OLEDs), solar cells, etc., to help improve the performance and efficiency of these devices.
In pharmaceutical research and development, one of them can be used as a key intermediate to synthesize a variety of biologically active compounds. Due to the special chemical structure of this substance, it is possible to interact with specific targets in organisms. For example, some studies have shown that derivatives based on it may inhibit or activate enzymes related to certain diseases, paving the way for the development of new therapeutic drugs, such as innovative drug development for specific cancers and neurological diseases. Second, in the optimization of pharmaceutical chemistry, it can be used as a starting point for structural modification. By modifying and modifying its chemical structure, such as introducing different substituents at specific locations, chemists can effectively adjust the physical and chemical properties of drug molecules, such as solubility, stability, and affinity with targets, thereby improving drug efficacy and reducing toxic and side effects.
In the chemical field, first of all, in organic synthetic chemistry, it is used as a multi-functional synthetic building block. With its unique structure, it can participate in various types of chemical reactions, such as nucleophilic substitution, electrophilic addition, etc., and then construct complex and diverse organic compounds, providing key raw materials for the synthesis of new materials and fine chemicals. Secondly, in the field of materials science, some compounds derived from 1% 2C2% 2C4% 2C5-tetrahydro-3-carbonyl indoles may exhibit unique optical and electrical properties, which are expected to be applied to the preparation of photovoltaic materials, such as organic Light Emitting Diodes (OLEDs), solar cells, etc., to help improve the performance and efficiency of these devices.
What are the storage conditions for 1,2,4,5-tetrachloro-3-nitrobenzene?
1% 2C2% 2C4% 2C5, which is the order of one, two, four, and five. The "four", "three" and "carboxylnaphthalene" involved are not to be investigated.
Four ", sexual activity, often need to be controlled in the air, and it should be controlled in the air. It should not be high, and it should be prevented from igniting. Because of its flammability, in case of open flame, high temperature, and oxidation can be strong. It must be the source of fire, the source of fire, and the container must be sealed.
" 3-carboxylnaphthalene "also has its way of hiding. It should be stored in a place where it is dry and dry, to avoid moisture and high temperature. Due to its chemical properties or environmental conditions, if it is damp, it may be caused by it. And it needs to be stored in parts such as oxidation and acid to prevent chemical reactions.
To the word "3", in this situation, or the quantity and value of the related chemical substances, etc., their existence also follows the above-mentioned characteristics of the materials. Moreover, the survival of such materials is determined by the environment, so as to ensure their integrity and prevent accidents.
Four ", sexual activity, often need to be controlled in the air, and it should be controlled in the air. It should not be high, and it should be prevented from igniting. Because of its flammability, in case of open flame, high temperature, and oxidation can be strong. It must be the source of fire, the source of fire, and the container must be sealed.
" 3-carboxylnaphthalene "also has its way of hiding. It should be stored in a place where it is dry and dry, to avoid moisture and high temperature. Due to its chemical properties or environmental conditions, if it is damp, it may be caused by it. And it needs to be stored in parts such as oxidation and acid to prevent chemical reactions.
To the word "3", in this situation, or the quantity and value of the related chemical substances, etc., their existence also follows the above-mentioned characteristics of the materials. Moreover, the survival of such materials is determined by the environment, so as to ensure their integrity and prevent accidents.
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