Linshang Chemical
PRODUCTS
2,4-Difluoro-5-Chloro-1-Nitrobenzene
Linshang Chemical
|
HS Code |
362733 |
| Chemical Formula | C6H2ClF2NO2 |
| Molar Mass | 193.54 g/mol |
| Appearance | Solid |
| Color | Yellowish solid |
| Melting Point | Data needed |
| Boiling Point | Data needed |
| Density | Data needed |
| Solubility In Water | Insoluble |
| Solubility In Organic Solvents | Soluble in common organic solvents like dichloromethane |
| Vapor Pressure | Data needed |
| Flash Point | Data needed |
| Hazard Class | Irritant (may cause skin, eye and respiratory irritation) |
As an accredited 2,4-Difluoro-5-Chloro-1-Nitrobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 500g of 2,4 - difluoro - 5 - chloro - 1 - nitrobenzene packaged in a sealed, corrosion - resistant container. |
| Storage | 2,4 - difluoro - 5 - chloro - 1 - nitrobenzene should be stored in a cool, dry, well - ventilated area, away from heat and ignition sources. Keep it in a tightly sealed container to prevent leakage. Store it separately from oxidizing agents, reducing agents, and bases as it may react. Avoid storing near food or beverages due to its toxic nature. |
| Shipping | 2,4 - difluoro - 5 - chloro - 1 - nitrobenzene is shipped in sealed, corrosion - resistant containers. It follows strict hazardous chemical shipping regulations to ensure safe transportation, avoiding exposure and potential risks during transit. |
Competitive 2,4-Difluoro-5-Chloro-1-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.
We will respond to you as soon as possible.
Tel: +8615365006308
Email: info@alchemist-chem.com
Where to Buy 2,4-Difluoro-5-Chloro-1-Nitrobenzene in China?
As a trusted 2,4-Difluoro-5-Chloro-1-Nitrobenzene 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 2,4-Difluoro-5-Chloro-1-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 main uses of 2,4-difluoro-5-chloro-1-nitrobenzene?
The compound 2% 2C4-diene-5-halogen-1-naphthylbenzene has important uses in many fields.
In the field of medicinal chemistry, its structural properties endow it with unique biological activities. After research, it has been found that the compound can act on specific biological targets, thereby regulating physiological processes in vivo. For example, it can be used as a potential anti-cancer drug component to inhibit the growth and spread of cancer cells by inhibiting the proliferation signaling pathway of cancer cells; in the treatment of neurodegenerative diseases, it may regulate the metabolism of neurotransmitters and alleviate the progression of the disease, providing an important structural basis for the development of related therapeutic drugs.
In the field of materials science, it exhibits unique optical and electrical properties. With its conjugated structure, it can be applied to the research and development of organic Light Emitting Diode (OLED) materials. As a light-emitting layer material, it can effectively improve the luminous efficiency and stability of OLED devices, promoting display screens to achieve higher brightness, richer colors and longer service life; in the field of organic solar cells, the compound is expected to be used as an electron transport or receptor material to enhance the absorption of light and charge transfer of batteries, improve the photoelectric conversion efficiency of solar cells, and provide new material options for the efficient utilization of renewable energy.
In organic synthesis chemistry, it is a key synthesis intermediate. Its complex and unique structure can be used as a starting material to construct more complex and diverse organic compounds through various organic reactions, such as nucleophilic substitution, addition reaction, etc. Researchers can flexibly modify and derive the structure of the target product according to the needs of the target product, providing convenience for the synthesis of organic molecules with specific functions and structures, and promoting the development and innovation of organic synthetic chemistry.
In the field of medicinal chemistry, its structural properties endow it with unique biological activities. After research, it has been found that the compound can act on specific biological targets, thereby regulating physiological processes in vivo. For example, it can be used as a potential anti-cancer drug component to inhibit the growth and spread of cancer cells by inhibiting the proliferation signaling pathway of cancer cells; in the treatment of neurodegenerative diseases, it may regulate the metabolism of neurotransmitters and alleviate the progression of the disease, providing an important structural basis for the development of related therapeutic drugs.
In the field of materials science, it exhibits unique optical and electrical properties. With its conjugated structure, it can be applied to the research and development of organic Light Emitting Diode (OLED) materials. As a light-emitting layer material, it can effectively improve the luminous efficiency and stability of OLED devices, promoting display screens to achieve higher brightness, richer colors and longer service life; in the field of organic solar cells, the compound is expected to be used as an electron transport or receptor material to enhance the absorption of light and charge transfer of batteries, improve the photoelectric conversion efficiency of solar cells, and provide new material options for the efficient utilization of renewable energy.
In organic synthesis chemistry, it is a key synthesis intermediate. Its complex and unique structure can be used as a starting material to construct more complex and diverse organic compounds through various organic reactions, such as nucleophilic substitution, addition reaction, etc. Researchers can flexibly modify and derive the structure of the target product according to the needs of the target product, providing convenience for the synthesis of organic molecules with specific functions and structures, and promoting the development and innovation of organic synthetic chemistry.
What are the physical properties of 2,4-difluoro-5-chloro-1-nitrobenzene?
2% 2C4-diene-5-bromo-1-naphthylbenzene is an organic compound with unique physical properties. This substance exists in a solid state at room temperature and pressure, and its molecules are closely arranged due to intermolecular forces. Looking at its appearance, it may be a white to light yellow crystalline powder with pure color and fine texture.
Regarding the melting point, the compound has a high melting point, and a higher temperature is required to melt it from a solid state to a liquid state. Due to the conjugated system in the molecular structure, the intermolecular forces are enhanced, so the energy required to break the lattice structure is very large. The boiling point is also correspondingly high, and in order to make it boil into a gaseous state, sufficient energy needs to be supplied to overcome the intermolecular attraction.
As for solubility, because the molecule has a certain hydrophobicity, the solubility in water is extremely low, and it is difficult for water molecules to form effective interactions with the compound molecule. However, in organic solvents such as dichloromethane, chloroform, toluene, etc., the solubility is relatively good. This is because there are similar van der Waals forces or other interactions between the organic solvent and the compound molecule, which can promote its uniform dispersion in the solvent.
The compound has a higher density than water, and if it is placed in water, it will sink to the bottom of the water. Its refractive index also has a specific value, which may have potential application value in the field of optics and can be used to identify and analyze the substance. In addition, the compound may have certain stability, but under specific conditions, such as high temperature, strong acid-base environment or specific catalysts, chemical reactions may occur and show different chemical activities.
Regarding the melting point, the compound has a high melting point, and a higher temperature is required to melt it from a solid state to a liquid state. Due to the conjugated system in the molecular structure, the intermolecular forces are enhanced, so the energy required to break the lattice structure is very large. The boiling point is also correspondingly high, and in order to make it boil into a gaseous state, sufficient energy needs to be supplied to overcome the intermolecular attraction.
As for solubility, because the molecule has a certain hydrophobicity, the solubility in water is extremely low, and it is difficult for water molecules to form effective interactions with the compound molecule. However, in organic solvents such as dichloromethane, chloroform, toluene, etc., the solubility is relatively good. This is because there are similar van der Waals forces or other interactions between the organic solvent and the compound molecule, which can promote its uniform dispersion in the solvent.
The compound has a higher density than water, and if it is placed in water, it will sink to the bottom of the water. Its refractive index also has a specific value, which may have potential application value in the field of optics and can be used to identify and analyze the substance. In addition, the compound may have certain stability, but under specific conditions, such as high temperature, strong acid-base environment or specific catalysts, chemical reactions may occur and show different chemical activities.
Is the chemical properties of 2,4-difluoro-5-chloro-1-nitrobenzene stable?
The properties of 2% 2C4-diene-5-bromo-1-naphthyl ether are not absolutely stable. The carbon-carbon double bond contained in its structure is easily attacked by electrophilic reagents due to the exposure of the electronic cloud of the π bond, and an addition reaction occurs. It can be added to the bromine elemental substance, destroying the original structure and affecting the stability. The halogen atom bromine, due to the large electronegativity of the bromine atom, has a polar C-Br bond. When the nucleophilic reagent exists, it is easy to trigger a nucleophilic substitution reaction. For example, when it is co-heated with sodium hydroxide aqueous solution, the bromine atom will be replaced by a hydroxyl group, changing the molecular structure and affecting its stable At the same time, although the naphthalene group has a conjugated system and has certain stability, the overall compound is limited in stability under various chemical environments due to the activity of double bonds and halogen atoms, and it is easy to participate in the reaction and change the structure.
What are the synthesis methods of 2,4-difluoro-5-chloro-1-nitrobenzene?
The synthesis method of 2% 2C4-diene-5-halogen-1-carbonylbenzene is not described directly in "Tiangong Kaiwu", but it can be derived from ancient chemical and pharmaceutical technologies.
Looking at ancient alchemy, alchemists are quite skilled in the extraction and synthesis of gold and stone minerals. To make this substance, you can first find benzene initial materials containing carbonyl groups, such as benzaldehyde. In ancient alchemy, benzaldehyde can be obtained by natural benzoin and hydrolysis.
Then, the halogen atom is introduced at the 5th position. Although there are no modern advanced halogenating reagents in ancient times, halogenated salts, such as sodium halide, potassium halide, etc., can be used, accompanied by a specific catalytic environment. In ancient times, or use alkaline substances such as plant ash to create a weakly alkaline reaction environment, so that the halogen atom nucleophilic substituted at the fifth position of the benzene ring.
As for the construction of 2,4-diene structure, we can learn from the ancient enylation method. In ancient times, there was a method of dehydrating alcohols to produce alkenes. Here, hydroxyl groups can be introduced into specific positions of the benzene ring first, and then try to dehydrate them into alkenes. For example, using natural plant extracts, fermentation and other methods, the benzene ring is connected to the hydroxyl group, and then calcined at high temperature, filled in an earthenware container, and the temperature is controlled in the stove to dehydrate the hydroxyl group to form a double bond, and gradually build a 2,4-diene structure.
Although the ancient techniques were simple, with the ancient people's insight into material changes and the accumulation of practical experience, with time and repeated trials, the synthesis of 2% 2C4-diene-5-halogen-1-carbonyl benzene may be obtained, which also shows that the ancient people are one of the wisdom of chemical synthesis.
Looking at ancient alchemy, alchemists are quite skilled in the extraction and synthesis of gold and stone minerals. To make this substance, you can first find benzene initial materials containing carbonyl groups, such as benzaldehyde. In ancient alchemy, benzaldehyde can be obtained by natural benzoin and hydrolysis.
Then, the halogen atom is introduced at the 5th position. Although there are no modern advanced halogenating reagents in ancient times, halogenated salts, such as sodium halide, potassium halide, etc., can be used, accompanied by a specific catalytic environment. In ancient times, or use alkaline substances such as plant ash to create a weakly alkaline reaction environment, so that the halogen atom nucleophilic substituted at the fifth position of the benzene ring.
As for the construction of 2,4-diene structure, we can learn from the ancient enylation method. In ancient times, there was a method of dehydrating alcohols to produce alkenes. Here, hydroxyl groups can be introduced into specific positions of the benzene ring first, and then try to dehydrate them into alkenes. For example, using natural plant extracts, fermentation and other methods, the benzene ring is connected to the hydroxyl group, and then calcined at high temperature, filled in an earthenware container, and the temperature is controlled in the stove to dehydrate the hydroxyl group to form a double bond, and gradually build a 2,4-diene structure.
Although the ancient techniques were simple, with the ancient people's insight into material changes and the accumulation of practical experience, with time and repeated trials, the synthesis of 2% 2C4-diene-5-halogen-1-carbonyl benzene may be obtained, which also shows that the ancient people are one of the wisdom of chemical synthesis.
What are the precautions for storing and transporting 2,4-difluoro-5-chloro-1-nitrobenzene?
2% 2C4-diene-5-bromo-1-naphthyl allyl ether This substance requires many matters to be paid attention to during storage and transportation.
Safety first. This substance may have specific chemical activities and potential hazards. When storing, it must be placed in a cool, dry and well-ventilated place, away from open flames and hot topics, to prevent the risk of fire and explosion. Due to its chemical properties, or reacts with other substances, it needs to be stored in isolation from oxidants, acids, bases, etc., and must not be mixed in storage and transportation to avoid dangerous chemical reactions.
Secondary packaging. Suitable packaging materials must be used to ensure a good seal to prevent leakage. The packaging material should be able to resist the corrosion of the substance, and key information such as the name of the chemical, hazardous characteristics and emergency treatment methods should be clearly marked on the outside of the package, so that the transportation and use personnel can clearly understand its nature.
Further transportation. The transportation process must be strictly in accordance with relevant regulations and operating procedures. When selecting a compliance transportation tool, the transportation personnel should be professionally trained and familiar with the chemical characteristics and emergency treatment methods. During transportation, closely monitor the environmental conditions such as temperature and humidity to avoid severe vibration and collision, and avoid leakage caused by package damage.
In addition, for storage and transportation sites, complete emergency equipment and protective equipment should be equipped, such as fire extinguishers, leakage emergency treatment tools, personal protective equipment, etc. Once there is an unexpected situation such as leakage, it can respond quickly, effectively dispose of it, and reduce the harm. Storage and transportation personnel should also exercise regularly to improve emergency response capabilities. In this way, 2% 2C4-diene-5-bromo-1-naphthyl allyl ether is safe during storage and transportation.
Safety first. This substance may have specific chemical activities and potential hazards. When storing, it must be placed in a cool, dry and well-ventilated place, away from open flames and hot topics, to prevent the risk of fire and explosion. Due to its chemical properties, or reacts with other substances, it needs to be stored in isolation from oxidants, acids, bases, etc., and must not be mixed in storage and transportation to avoid dangerous chemical reactions.
Secondary packaging. Suitable packaging materials must be used to ensure a good seal to prevent leakage. The packaging material should be able to resist the corrosion of the substance, and key information such as the name of the chemical, hazardous characteristics and emergency treatment methods should be clearly marked on the outside of the package, so that the transportation and use personnel can clearly understand its nature.
Further transportation. The transportation process must be strictly in accordance with relevant regulations and operating procedures. When selecting a compliance transportation tool, the transportation personnel should be professionally trained and familiar with the chemical characteristics and emergency treatment methods. During transportation, closely monitor the environmental conditions such as temperature and humidity to avoid severe vibration and collision, and avoid leakage caused by package damage.
In addition, for storage and transportation sites, complete emergency equipment and protective equipment should be equipped, such as fire extinguishers, leakage emergency treatment tools, personal protective equipment, etc. Once there is an unexpected situation such as leakage, it can respond quickly, effectively dispose of it, and reduce the harm. Storage and transportation personnel should also exercise regularly to improve emergency response capabilities. In this way, 2% 2C4-diene-5-bromo-1-naphthyl allyl ether is safe during storage and transportation.
Scan to WhatsApp
