Linshang Chemical
PRODUCTS
5-Bromo-3-Chloro-2-Fluoronitrobenzene
Linshang Chemical
|
HS Code |
251228 |
| Chemical Formula | C6H2BrClFNO2 |
| Appearance | Solid (Typical) |
| Color | Yellow to brownish solid |
| Odor | Typical organic chemical odor |
| Solubility In Water | Low solubility (Organic nitro - halogenated benzene compounds are generally hydrophobic) |
| Vapor Pressure | Low (Typical for such solid aromatic compounds) |
| Stability | Stable under normal conditions, but may react with strong oxidizing agents |
As an accredited 5-Bromo-3-Chloro-2-Fluoronitrobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 5 - bromo - 3 - chloro - 2 - fluoronitrobenzene in 1 - kg bottles for chemical packaging. |
| Storage | 5 - Bromo - 3 - chloro - 2 - fluoronitrobenzene should be stored in a cool, dry, well - ventilated area, away from heat sources and open flames. Keep it in a tightly - sealed container to prevent leakage. Due to its chemical nature, store it separately from oxidizing agents, reducing agents, and substances that could react with it, in a place accessible only to trained personnel. |
| Shipping | 5 - bromo - 3 - chloro - 2 - fluoronitrobenzene is a chemical. Shipping should be in properly sealed, labeled containers. Follow regulations for hazardous chemicals, ensuring secure packaging to prevent leakage during transit. |
Competitive 5-Bromo-3-Chloro-2-Fluoronitrobenzene 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.
We will respond to you as soon as possible.
Tel: +8615365006308
Email: info@alchemist-chem.com
Where to Buy 5-Bromo-3-Chloro-2-Fluoronitrobenzene in China?
As a trusted 5-Bromo-3-Chloro-2-Fluoronitrobenzene manufacturer, we deliver:
Factory-Direct Value: Competitive pricing with no middleman markups, tailored for bulk orders and project-scale requirements.
Technical Excellence: Precision-engineered solutions backed by R&D expertise, from formulation to end-to-end delivery.
Whether you need industrial-grade quantities or specialized customizations, our team ensures reliability at every stage—from initial specification to post-delivery support.
As a leading 5-Bromo-3-Chloro-2-Fluoronitrobenzene 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 physical properties of 5-bromo-3-chloro-2-fluoronitrobenzene?
5-Hydroxy-3-amine-2-furanylacronaldehyde is a unique organic compound. Its physical properties are quite unique, let me tell them one by one.
Looking at its properties, under room temperature and pressure, 5-hydroxy- 3-amine-2-furanylacronaldehyde is mostly in a solid state, which is due to the intermolecular force. Its crystalline structure is dense, resulting in the appearance of powder or fine crystals. The particles are delicate and uniform, and the luster is soft. It is not as dazzling as metal, nor as transparent as glass. It has a simple state.
As for the color, this object often shows a light yellow to light brown color, just like the first yellow of autumn wood leaves, and the morning light brushes against thin clouds. The formation of this color is due to the distribution and transition of electron clouds in the molecular structure, and the specific chemical bonds absorb and reflect specific wavelengths of light, resulting in this unique color.
Smell its smell, there is a faint and specific fragrance, neither rich and pungent fragrance nor rancid and unpleasant smell, just like the faint orchid fragrance blowing in the breeze, elegant and long-lasting, and then under the fine smell, it has an indescribable quality. This smell is related to the volatility of molecules and the nature of functional groups.
When it comes to solubility, 5-hydroxy- 3-amine-2-furanyl acronaldehyde exhibits a certain solubility in organic solvents, such as ethanol and acetone. Ethanol, with its moderate polarity, can form hydrogen bonds and other interactions with the compound molecules, so that the molecules can be dispersed in it and form a uniform solution. However, in water, its solubility is relatively limited. Although the polarity of water molecules is strong, the structural characteristics of the compound molecule make it interact with water molecules to a degree of insufficient solubility and can only be slightly soluble in water.
Its melting point is also one of the important physical properties. The melting point has been determined to be within a specific temperature range. This temperature range is determined by the balance of intermolecular forces and lattice energy. When heated, the molecule obtains enough energy to overcome the lattice binding, so that it changes from a solid state to a liquid state. This characteristic of melting point can be used for the identification and identification of the purity of compounds.
The density of 5-hydroxyl-3-amine-2-furanylacronaldehyde also has its own unique value compared with common organic solvents or water. This density reflects the degree of tight packing and relative mass of the molecule, and is a key parameter when studying its distribution and behavior in mixed systems.
In summary, 5-hydroxy- 3-amine-2-furanoacronaldehyde has its unique physical properties, which may have wonderful uses in many fields such as chemistry and biology, and we need to explore it in depth.
Looking at its properties, under room temperature and pressure, 5-hydroxy- 3-amine-2-furanylacronaldehyde is mostly in a solid state, which is due to the intermolecular force. Its crystalline structure is dense, resulting in the appearance of powder or fine crystals. The particles are delicate and uniform, and the luster is soft. It is not as dazzling as metal, nor as transparent as glass. It has a simple state.
As for the color, this object often shows a light yellow to light brown color, just like the first yellow of autumn wood leaves, and the morning light brushes against thin clouds. The formation of this color is due to the distribution and transition of electron clouds in the molecular structure, and the specific chemical bonds absorb and reflect specific wavelengths of light, resulting in this unique color.
Smell its smell, there is a faint and specific fragrance, neither rich and pungent fragrance nor rancid and unpleasant smell, just like the faint orchid fragrance blowing in the breeze, elegant and long-lasting, and then under the fine smell, it has an indescribable quality. This smell is related to the volatility of molecules and the nature of functional groups.
When it comes to solubility, 5-hydroxy- 3-amine-2-furanyl acronaldehyde exhibits a certain solubility in organic solvents, such as ethanol and acetone. Ethanol, with its moderate polarity, can form hydrogen bonds and other interactions with the compound molecules, so that the molecules can be dispersed in it and form a uniform solution. However, in water, its solubility is relatively limited. Although the polarity of water molecules is strong, the structural characteristics of the compound molecule make it interact with water molecules to a degree of insufficient solubility and can only be slightly soluble in water.
Its melting point is also one of the important physical properties. The melting point has been determined to be within a specific temperature range. This temperature range is determined by the balance of intermolecular forces and lattice energy. When heated, the molecule obtains enough energy to overcome the lattice binding, so that it changes from a solid state to a liquid state. This characteristic of melting point can be used for the identification and identification of the purity of compounds.
The density of 5-hydroxyl-3-amine-2-furanylacronaldehyde also has its own unique value compared with common organic solvents or water. This density reflects the degree of tight packing and relative mass of the molecule, and is a key parameter when studying its distribution and behavior in mixed systems.
In summary, 5-hydroxy- 3-amine-2-furanoacronaldehyde has its unique physical properties, which may have wonderful uses in many fields such as chemistry and biology, and we need to explore it in depth.
What are the chemical properties of 5-bromo-3-chloro-2-fluoronitrobenzene?
5-Hydroxy-3-mercapto-2-furanoyl hydrazide, which is white to light yellow crystalline powder and stable at room temperature and pressure. Its solubility is quite characteristic, it can be dissolved in dimethyl sulfoxide, but it is difficult to dissolve in water, ethanol and dichloromethane.
In terms of chemical activity, the hydroxyl groups, mercapto groups and hydrazide groups in 5-hydroxy-3-mercapto-2-furanoyl hydrazide are all reactive. Hydroxyl groups can participate in esterification reactions. Under the catalysis of acids or bases, they react with carboxylic acids to form corresponding ester compounds. For example, when reacting with acetic acid, under the catalysis of sulfuric acid and heating conditions, acetate esters can be formed. The activity of the sulfhydryl group should not be underestimated. It is easily oxidized. In the air, it will gradually be oxidized to form disulfide bonds. Moreover, the sulfhydryl group can react specifically with heavy metal ions to form stable complexes. When it encounters mercury ions, it will quickly bind to form insoluble precipitates, which can be used to detect and remove mercury ions from the environment.
The acyl hydrazide group can condensate with alaldehyde and ketone to form hydrazone compounds. For example, at the appropriate temperature and in the presence of a catalyst, it reacts with benzaldehyde to form benzaldehyde hydrazone. At the same time, the acyl hydrazide group has the ability to coordinate certain metal ions and can form metal complexes. These complexes have shown potential application value in the fields of catalysis and materials science.
In the field of organic synthesis, 5-hydroxy-3-mercapto-2-furanoyl hydrazide is often used as a key intermediate. Due to the existence of multiple active groups, it can construct more complex organic compounds through a series of chemical reactions, providing an important material basis for drug development and material synthesis.
In terms of chemical activity, the hydroxyl groups, mercapto groups and hydrazide groups in 5-hydroxy-3-mercapto-2-furanoyl hydrazide are all reactive. Hydroxyl groups can participate in esterification reactions. Under the catalysis of acids or bases, they react with carboxylic acids to form corresponding ester compounds. For example, when reacting with acetic acid, under the catalysis of sulfuric acid and heating conditions, acetate esters can be formed. The activity of the sulfhydryl group should not be underestimated. It is easily oxidized. In the air, it will gradually be oxidized to form disulfide bonds. Moreover, the sulfhydryl group can react specifically with heavy metal ions to form stable complexes. When it encounters mercury ions, it will quickly bind to form insoluble precipitates, which can be used to detect and remove mercury ions from the environment.
The acyl hydrazide group can condensate with alaldehyde and ketone to form hydrazone compounds. For example, at the appropriate temperature and in the presence of a catalyst, it reacts with benzaldehyde to form benzaldehyde hydrazone. At the same time, the acyl hydrazide group has the ability to coordinate certain metal ions and can form metal complexes. These complexes have shown potential application value in the fields of catalysis and materials science.
In the field of organic synthesis, 5-hydroxy-3-mercapto-2-furanoyl hydrazide is often used as a key intermediate. Due to the existence of multiple active groups, it can construct more complex organic compounds through a series of chemical reactions, providing an important material basis for drug development and material synthesis.
What are the synthesis methods of 5-bromo-3-chloro-2-fluoronitrobenzene?
To prepare 5-hydroxyl-3-alkane-2-furanoyl benzene, there are many methods, each with its own strengths. The following are detailed preparation methods.
One is a chemical synthesis method. Using a specific organic compound as the starting material, a series of chemical reactions are used to achieve the goal. For example, a compound containing a furan structure and a benzene ring and a specific functional group can be selected. Under suitable reaction conditions, such as in a specific catalyst, temperature and pressure environment, the two can undergo condensation reaction, and then construct the basic structure of 5-hydroxyl-3-alkane-2-furanoyl benzene. Subsequent steps such as functional group modification and purification may be required to obtain a high-purity product. The advantage of this method is that the reaction path can be precisely designed according to the needs, and the purity of the product is relatively easy to control; however, its shortcomings are also obvious. The reaction steps may be cumbersome, the cost of raw materials may be high, and the reaction conditions are strict, so precise control is required, otherwise the yield and purity of the product will be affected.
The second is biosynthesis. The catalytic properties of microorganisms or enzymes can be used to achieve synthesis. Under specific culture conditions, some microorganisms can use specific substrates as raw materials to produce target products through complex metabolic pathways in the body. Or extract enzymes with specific catalytic activities, simulate the environment in vivo in vitro, and catalyze the substrate to generate 5-hydroxyl-3-alkane-2-furanoyl benzene. This method has the advantages of green environmental protection, mild reaction conditions, and high biocatalyst specificity, which can reduce side reactions. However, there are also disadvantages. The extraction and purification process of microbial culture or enzymes is complicated, the cost is high, and the biological system is sensitive to environmental factors, which easily leads to poor production stability.
The third is the extraction method of natural products. Some plants, microorganisms and other organisms in nature may contain this compound. It can be obtained from natural resources by appropriate extraction methods, such as solvent extraction, supercritical fluid extraction, etc. The product obtained by this method is naturally pure or has unique biological activity. However, natural resources are limited, the extraction process may affect the environment, and the content is usually low, the extraction efficiency is not high, and a large number of natural raw materials are required to meet the demand.
One is a chemical synthesis method. Using a specific organic compound as the starting material, a series of chemical reactions are used to achieve the goal. For example, a compound containing a furan structure and a benzene ring and a specific functional group can be selected. Under suitable reaction conditions, such as in a specific catalyst, temperature and pressure environment, the two can undergo condensation reaction, and then construct the basic structure of 5-hydroxyl-3-alkane-2-furanoyl benzene. Subsequent steps such as functional group modification and purification may be required to obtain a high-purity product. The advantage of this method is that the reaction path can be precisely designed according to the needs, and the purity of the product is relatively easy to control; however, its shortcomings are also obvious. The reaction steps may be cumbersome, the cost of raw materials may be high, and the reaction conditions are strict, so precise control is required, otherwise the yield and purity of the product will be affected.
The second is biosynthesis. The catalytic properties of microorganisms or enzymes can be used to achieve synthesis. Under specific culture conditions, some microorganisms can use specific substrates as raw materials to produce target products through complex metabolic pathways in the body. Or extract enzymes with specific catalytic activities, simulate the environment in vivo in vitro, and catalyze the substrate to generate 5-hydroxyl-3-alkane-2-furanoyl benzene. This method has the advantages of green environmental protection, mild reaction conditions, and high biocatalyst specificity, which can reduce side reactions. However, there are also disadvantages. The extraction and purification process of microbial culture or enzymes is complicated, the cost is high, and the biological system is sensitive to environmental factors, which easily leads to poor production stability.
The third is the extraction method of natural products. Some plants, microorganisms and other organisms in nature may contain this compound. It can be obtained from natural resources by appropriate extraction methods, such as solvent extraction, supercritical fluid extraction, etc. The product obtained by this method is naturally pure or has unique biological activity. However, natural resources are limited, the extraction process may affect the environment, and the content is usually low, the extraction efficiency is not high, and a large number of natural raw materials are required to meet the demand.
What are the main uses of 5-bromo-3-chloro-2-fluoronitrobenzene?
The main use of 5-3-3-2-sea clam-based materials is found in "Tiangong".
These materials are first used in ash. In this method, 5-3-3-2-sea clam-based materials are placed in the soil and calcined by fire. High-grade calcined and calcined, the clam melts lime. Lime has a wide range of uses, and it can be used for building things. In ancient times, when building cities and houses, lime was often mixed with sediment and other materials to make the building more solid. For example, in the city, the mixing of lime, soil, stone, etc., can increase the degree of resistance to rain and external forces.
Furthermore, 5-3-2-mussel-based lime can also be used in the field. Scattered on the field, it can reduce the acidity of the soil. If the field soil is slightly acidic, lime can neutralize the acidity, improve the soil environment, and is beneficial to crop growth. And lime also has the effect of removing bacteria, which can reduce the breeding of diseases and diseases in the field and ensure the harvest of crops.
In addition, in the fields of production, mussel production may also have its use. "Tiangong" does not specify the application in this regard, but it is recommended by its nature, or it can be used to complete some parts of the environment, such as the degree of acidity of leaven, etc., the product of production may have a certain effect. Therefore, 5-3-2-sea mussel-based calcination into lime is an important function in manufacturing, engineering, and other aspects, and is an indispensable material for the ancient people's life and production.
These materials are first used in ash. In this method, 5-3-3-2-sea clam-based materials are placed in the soil and calcined by fire. High-grade calcined and calcined, the clam melts lime. Lime has a wide range of uses, and it can be used for building things. In ancient times, when building cities and houses, lime was often mixed with sediment and other materials to make the building more solid. For example, in the city, the mixing of lime, soil, stone, etc., can increase the degree of resistance to rain and external forces.
Furthermore, 5-3-2-mussel-based lime can also be used in the field. Scattered on the field, it can reduce the acidity of the soil. If the field soil is slightly acidic, lime can neutralize the acidity, improve the soil environment, and is beneficial to crop growth. And lime also has the effect of removing bacteria, which can reduce the breeding of diseases and diseases in the field and ensure the harvest of crops.
In addition, in the fields of production, mussel production may also have its use. "Tiangong" does not specify the application in this regard, but it is recommended by its nature, or it can be used to complete some parts of the environment, such as the degree of acidity of leaven, etc., the product of production may have a certain effect. Therefore, 5-3-2-sea mussel-based calcination into lime is an important function in manufacturing, engineering, and other aspects, and is an indispensable material for the ancient people's life and production.
What are the precautions for 5-bromo-3-chloro-2-fluoronitrobenzene during storage and transportation?
For 5-% ether-3-alkane-2-enyl aminonaphthalenes, when hiding and transporting, all kinds of things should be paid attention to.
When hiding, the first place is where you are. It is advisable to choose a dry and cool place to avoid sun exposure and wet soaking. If it is in a warm and humid place, this thing may be at risk of deterioration and damage its quality. And it must be separated from other things, especially with strong oxidizing agents and strong acidic substances, in order to prevent severe reactions and dangers.
Furthermore, its utensils must also be suitable. When storing it in a secret utensil, it should not be vented outside. The material of the utensil is also exquisite, preferably glass, ceramics or specific plastic materials, because it should be less integrated with the object, so as to ensure the stability of its quality.
As for the time of transportation, be careful on the road to prevent it from being shaken and collided. The road of driving should be slow and stable, avoiding sudden brakes and sudden starts, so as not to break the device and leak the object. The operator should also be aware of this materiality and prepare corresponding measures. If there is a leak, they can respond to it quickly.
In addition, the route of transportation should be kept out of the privacy of people, so as not to endanger the common people. And on the transport equipment, clearly mark the nature and danger of this object, so that those who see it can be alerted.
On the way, it is also necessary to check the complete damage of the device to see if there is any leakage. If there is a slight damage to the device, or there is a gas smell, it should not be slack at the speed.
In short, when the 5-% ether-3-alkane-2-alkenyl aminonaphthalene is hidden and transported, all the details are related to its quality and safety, and it must be done with caution.
When hiding, the first place is where you are. It is advisable to choose a dry and cool place to avoid sun exposure and wet soaking. If it is in a warm and humid place, this thing may be at risk of deterioration and damage its quality. And it must be separated from other things, especially with strong oxidizing agents and strong acidic substances, in order to prevent severe reactions and dangers.
Furthermore, its utensils must also be suitable. When storing it in a secret utensil, it should not be vented outside. The material of the utensil is also exquisite, preferably glass, ceramics or specific plastic materials, because it should be less integrated with the object, so as to ensure the stability of its quality.
As for the time of transportation, be careful on the road to prevent it from being shaken and collided. The road of driving should be slow and stable, avoiding sudden brakes and sudden starts, so as not to break the device and leak the object. The operator should also be aware of this materiality and prepare corresponding measures. If there is a leak, they can respond to it quickly.
In addition, the route of transportation should be kept out of the privacy of people, so as not to endanger the common people. And on the transport equipment, clearly mark the nature and danger of this object, so that those who see it can be alerted.
On the way, it is also necessary to check the complete damage of the device to see if there is any leakage. If there is a slight damage to the device, or there is a gas smell, it should not be slack at the speed.
In short, when the 5-% ether-3-alkane-2-alkenyl aminonaphthalene is hidden and transported, all the details are related to its quality and safety, and it must be done with caution.
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