Linshang Chemical
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Benzene, 4-Chloro-1-Methoxy-2-Nitro-
Linshang Chemical
|
HS Code |
869964 |
| Chemical Formula | C7H6ClNO3 |
| Molar Mass | 187.58 g/mol |
| Appearance | Solid (likely, based on similar compounds) |
| Solubility In Water | Low solubility, as nitro and chloro groups reduce water - solubility of the aromatic ring |
| Solubility In Organic Solvents | Soluble in common organic solvents like ethanol, acetone, due to its non - polar aromatic structure |
| Vapor Pressure | Low vapor pressure, typical for a relatively high - molecular - weight solid organic compound |
As an accredited Benzene, 4-Chloro-1-Methoxy-2-Nitro- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 500g of 4 - chloro - 1 - methoxy - 2 - nitro - benzene in sealed chemical - grade container. |
| Storage | Store “Benzene, 4 - chloro - 1 - methoxy - 2 - nitro -” in a cool, well - ventilated area away from heat, sparks, and open flames. Keep it in a tightly closed container, preferably made of corrosion - resistant material. Isolate it from oxidizing agents, reducing agents, and other reactive substances to prevent chemical reactions. |
| Shipping | Shipping of "Benzene, 4 - chloro - 1 - methoxy - 2 - nitro -" must comply with strict regulations. It's a hazardous chemical, so it requires proper packaging, labeling indicating its dangerous nature, and transport via approved carriers following safety protocols. |
Competitive Benzene, 4-Chloro-1-Methoxy-2-Nitro- 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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What are the physical properties of 4-chloro-1-methoxy-2-nitrobenzene
"Mercury, commonly known as mercury, is a liquid metal at room temperature, with a silver luster, high density, good fluidity, easy to volatilize, and its vapor is toxic." "Methyl mercury is very toxic. After entering the human body, it is easy to accumulate and difficult to discharge, damaging the nervous system and causing great harm." "Benzyl chloride, a colorless and transparent liquid, has an irritating odor, is insoluble in water, and can be miscible in organic solvents such as ethanol and ether. It is flammable in the event of an open flame or hot topic. It is decomposed by hot topic to produce toxic corrosive flue gas."
Mercury is mostly found in ores in nature. In the past, it was mostly refined with cinnabar. Its liquid shape, flowing like mercury, has a luster like silver, so it is called this. Due to its high density, it flows quickly when dumped. However, its volatile nature causes its vapor to spread in the air, and it is easy to be poisoned if inhaled.
Methylmercury is a compound that binds mercury to methyl groups. In the environment, microorganisms can convert mercury into methylmercury. Because of its lipid solubility, it is easy to penetrate biofilms and accumulate in organisms. Aquatic organisms such as fish often accumulate methylmercury. If people eat it, methylmercury enters the body, damaging the nervous system, causing speech, vision, movement disorders, etc.
Benzyl chloride, a commonly used raw material for organic synthesis in industry. Its colorless and transparent shape is compatible with many organic solvents, making it easy to participate in various chemical reactions. However, it has an irritating smell, irritating to the eyes, respiratory tract, etc. And flammable, in case of open flames and hot topics, it is easy to cause fires, and the toxic fumes generated by decomposition also endanger the environment and personal safety.
These three have their own characteristics, which affect human life and industrial production. It is necessary to use them properly, prevent them, and avoid their harm.
Mercury is mostly found in ores in nature. In the past, it was mostly refined with cinnabar. Its liquid shape, flowing like mercury, has a luster like silver, so it is called this. Due to its high density, it flows quickly when dumped. However, its volatile nature causes its vapor to spread in the air, and it is easy to be poisoned if inhaled.
Methylmercury is a compound that binds mercury to methyl groups. In the environment, microorganisms can convert mercury into methylmercury. Because of its lipid solubility, it is easy to penetrate biofilms and accumulate in organisms. Aquatic organisms such as fish often accumulate methylmercury. If people eat it, methylmercury enters the body, damaging the nervous system, causing speech, vision, movement disorders, etc.
Benzyl chloride, a commonly used raw material for organic synthesis in industry. Its colorless and transparent shape is compatible with many organic solvents, making it easy to participate in various chemical reactions. However, it has an irritating smell, irritating to the eyes, respiratory tract, etc. And flammable, in case of open flames and hot topics, it is easy to cause fires, and the toxic fumes generated by decomposition also endanger the environment and personal safety.
These three have their own characteristics, which affect human life and industrial production. It is necessary to use them properly, prevent them, and avoid their harm.
What are the chemical properties of 4-chloro-1-methoxy-2-nitrobenzene?
The physicochemical properties of Fu 4 + -1 -methylphenyl-2 -carbonylphenyl are important for investigation.
The basic body is nuclear, and it can generate substitutions and antibodies, such as the generation of antibodies to generate ethers. And the alkenyl group can form alkenes from water, or oxidize to alters, ketones and even carboxylic acids. Due to the large property of oxygen atoms in the alkyl group, the property of oxygen is low, so that the material containing this group can be formed, which affects its melting, solubility and other physical properties.
As for carbonyl phenyl groups, carbonyl groups are the most toxic and chemically active. Carbonyl carbon atoms are toxic and vulnerable to nuclear attack, and the addition of alkenyl nuclei is reversed. For example, the addition of alcohol to generate hemialdehyde and aldehyde. Phenyl and aromatic groups have special properties because of their high degree of subcloud domain. However, phenyl groups can also be substituted and reversed, such as benzene substitution, because the cloud density of benzene is high, it is easy to attract benzene.
, the combination of these three is formed, and its chemical properties are affected by the interaction of each group. Each group does not exist in isolation, and each other controls and shapes each other, jointly determining the surface of this object in chemical reactions and physical environments.
The basic body is nuclear, and it can generate substitutions and antibodies, such as the generation of antibodies to generate ethers. And the alkenyl group can form alkenes from water, or oxidize to alters, ketones and even carboxylic acids. Due to the large property of oxygen atoms in the alkyl group, the property of oxygen is low, so that the material containing this group can be formed, which affects its melting, solubility and other physical properties.
As for carbonyl phenyl groups, carbonyl groups are the most toxic and chemically active. Carbonyl carbon atoms are toxic and vulnerable to nuclear attack, and the addition of alkenyl nuclei is reversed. For example, the addition of alcohol to generate hemialdehyde and aldehyde. Phenyl and aromatic groups have special properties because of their high degree of subcloud domain. However, phenyl groups can also be substituted and reversed, such as benzene substitution, because the cloud density of benzene is high, it is easy to attract benzene.
, the combination of these three is formed, and its chemical properties are affected by the interaction of each group. Each group does not exist in isolation, and each other controls and shapes each other, jointly determining the surface of this object in chemical reactions and physical environments.
What are the main uses of 4-chloro-1-methoxy-2-nitrobenzene?
4 + -Deuterium-1-methoxy-2-carboxypyridine, which has a wide range of uses.
In the field of medicinal chemistry, it can be used as a key intermediate for the synthesis of a variety of drugs with specific biological activities. The presence of the gainpyridine ring and functional groups such as carboxyl and methoxy gives it unique chemical properties and can interact with specific targets in organisms. By modifying and modifying its structure by chemical synthesis, derivatives with different pharmacological activities can be obtained, or as antibacterial drugs, by inhibiting bacterial cell wall synthesis, interfering with bacterial protein synthesis and other mechanisms, killing or inhibiting bacterial growth; or as anticancer drugs, by inhibiting tumor cell proliferation, inducing tumor cell apoptosis and other pathways, play an anti-cancer effect.
In the field of materials science, 4 + -deuterium-1-methoxy-2-carboxypyridine also has important value. Due to its special structure, it can participate in the synthesis of polymer materials. When preparing functional polymers, introducing them into the polymer chain as monomers can endow the materials with unique properties such as good solubility, thermal stability, and optical properties. For example, in some optical materials, it can change the refractive index and fluorescence properties of the material, making the material suitable for optoelectronic devices, such as organic Light Emitting Diodes (OLEDs), to improve the luminous efficiency and stability of the device.
In the field of organic synthetic chemistry, it is an extremely useful synthetic building block. With the reactivity of carboxyl groups and methoxy groups, more complex organic molecular structures can be constructed through esterification, etherification, nucleophilic substitution and many other reactions. Chemists can use them as starting materials to synthesize organic compounds with specific spatial structures and functions by ingeniously designing reaction routes, providing new ways and methods for the development of organic synthetic chemistry.
In the field of medicinal chemistry, it can be used as a key intermediate for the synthesis of a variety of drugs with specific biological activities. The presence of the gainpyridine ring and functional groups such as carboxyl and methoxy gives it unique chemical properties and can interact with specific targets in organisms. By modifying and modifying its structure by chemical synthesis, derivatives with different pharmacological activities can be obtained, or as antibacterial drugs, by inhibiting bacterial cell wall synthesis, interfering with bacterial protein synthesis and other mechanisms, killing or inhibiting bacterial growth; or as anticancer drugs, by inhibiting tumor cell proliferation, inducing tumor cell apoptosis and other pathways, play an anti-cancer effect.
In the field of materials science, 4 + -deuterium-1-methoxy-2-carboxypyridine also has important value. Due to its special structure, it can participate in the synthesis of polymer materials. When preparing functional polymers, introducing them into the polymer chain as monomers can endow the materials with unique properties such as good solubility, thermal stability, and optical properties. For example, in some optical materials, it can change the refractive index and fluorescence properties of the material, making the material suitable for optoelectronic devices, such as organic Light Emitting Diodes (OLEDs), to improve the luminous efficiency and stability of the device.
In the field of organic synthetic chemistry, it is an extremely useful synthetic building block. With the reactivity of carboxyl groups and methoxy groups, more complex organic molecular structures can be constructed through esterification, etherification, nucleophilic substitution and many other reactions. Chemists can use them as starting materials to synthesize organic compounds with specific spatial structures and functions by ingeniously designing reaction routes, providing new ways and methods for the development of organic synthetic chemistry.
What is the preparation method of 4-chloro-1-methoxy-2-nitrobenzene?
To prepare 4-hydroxyl-1-methoxy-2-furanyl, the following method can be followed.
First take an appropriate amount of starting materials, and preferably a furan derivative with a suitable substituent. In a clean reaction vessel, put this furan derivative, and properly dissolve it in an organic solvent such as dichloromethane and tetrahydrofuran to form a uniform solution. The organic solvent needs to be dried in advance to avoid water interference in the reaction.
Then, slowly add a specific reagent to introduce the methoxy group. A suitable methylation reagent can be selected, such as a combination of iodomethane and a base (such as potassium carbonate, etc.). Under gentle stirring, control the reaction temperature to an appropriate range, usually between low temperature and room temperature, such as 0 ° C to 25 ° C, so that the reaction can proceed smoothly. During this process, pay close attention to the changes in the reaction system, or monitor the reaction progress by means of thin-layer chromatography to ensure the precise introduction of methoxy groups into the target position.
When the reaction of introducing methoxy groups reaches the expected degree, the reaction solution is preliminarily treated. Remove part of the organic solvent by a suitable method, such as vacuum distillation, then add an appropriate amount of water and the organic solvent for extraction, collect the organic phase after stratification, and then dry the organic phase with a desiccant such as anhydrous sodium sulfate to remove the remaining moisture.
Next, add a reagent capable of generating hydroxyl groups to the organic phase. Specific oxidizing reagents, such as mild oxidizing agents such as m-chloroperoxybenzoic acid, can be used to react with furan derivatives containing methoxy groups under suitable reaction conditions to generate 4-hydroxyl-1-methoxy-2-furan groups. This step also requires precise control of the reaction conditions, and careful control of temperature and reaction time to prevent excessive oxidation or side reactions.
After the reaction is completed, the product is separated and purified. Column chromatography can be used to select suitable stationary phase and eluent, effectively separate the target product from impurities, collect the eluent containing pure products, and then concentrate under reduced pressure to finally obtain pure 4-hydroxyl-1-methoxy-2-furan. The whole preparation process requires strict control of the reaction conditions of each step and careful operation to obtain the ideal product.
First take an appropriate amount of starting materials, and preferably a furan derivative with a suitable substituent. In a clean reaction vessel, put this furan derivative, and properly dissolve it in an organic solvent such as dichloromethane and tetrahydrofuran to form a uniform solution. The organic solvent needs to be dried in advance to avoid water interference in the reaction.
Then, slowly add a specific reagent to introduce the methoxy group. A suitable methylation reagent can be selected, such as a combination of iodomethane and a base (such as potassium carbonate, etc.). Under gentle stirring, control the reaction temperature to an appropriate range, usually between low temperature and room temperature, such as 0 ° C to 25 ° C, so that the reaction can proceed smoothly. During this process, pay close attention to the changes in the reaction system, or monitor the reaction progress by means of thin-layer chromatography to ensure the precise introduction of methoxy groups into the target position.
When the reaction of introducing methoxy groups reaches the expected degree, the reaction solution is preliminarily treated. Remove part of the organic solvent by a suitable method, such as vacuum distillation, then add an appropriate amount of water and the organic solvent for extraction, collect the organic phase after stratification, and then dry the organic phase with a desiccant such as anhydrous sodium sulfate to remove the remaining moisture.
Next, add a reagent capable of generating hydroxyl groups to the organic phase. Specific oxidizing reagents, such as mild oxidizing agents such as m-chloroperoxybenzoic acid, can be used to react with furan derivatives containing methoxy groups under suitable reaction conditions to generate 4-hydroxyl-1-methoxy-2-furan groups. This step also requires precise control of the reaction conditions, and careful control of temperature and reaction time to prevent excessive oxidation or side reactions.
After the reaction is completed, the product is separated and purified. Column chromatography can be used to select suitable stationary phase and eluent, effectively separate the target product from impurities, collect the eluent containing pure products, and then concentrate under reduced pressure to finally obtain pure 4-hydroxyl-1-methoxy-2-furan. The whole preparation process requires strict control of the reaction conditions of each step and careful operation to obtain the ideal product.
What are the precautions for 4-chloro-1-methoxy-2-nitrobenzene in storage and transportation?
If there is 4 + -1-methoxy-2-benzyl ether, there is no need to pay attention to it when it is not stored.
First of all, this substance has a lot of chemical activity, and its properties may be affected by external components. Therefore, if it is not stored, it must be dry, dry, and pass through a good place. If it is in a tidal environment, it is feared that there will be reactions such as hydrolysis, which will cause the substance to be damaged. For example, the moisture contained in the tidal air may interact with its active radical phase, change its chemical properties, and lose its original properties.
Second, the control of the degree also needs to be controlled. High-temperature environments can promote the rate of transformation and reaction, and even lead to uncontrollable reactions. Therefore, avoid direct sunlight and do not expose to high temperatures. If the degree of preservation is high, the compound may decompose or polymerize, which is not what we want.
Furthermore, on the way, it is necessary to prevent it from being shaken or collided. This external force may break its molecules, or cause local reactions. And it is necessary to isolate other chemical products. Due to the incompatibility of different materials, or incompatible characteristics, once connected, it may cause severe reactions and endanger the safety of the product.
In addition, the solid density of the package cannot be ignored. A well-sealed package can block the drying of external air, moisture, etc., and keep the material safe during storage and storage. If the package is intact, external factors are easily intrusive, causing the product to be damaged.
Therefore, the storage of 4 + -1-methoxy-2-benzyl ether should be done with caution and attention should be paid to the safety of the product.
First of all, this substance has a lot of chemical activity, and its properties may be affected by external components. Therefore, if it is not stored, it must be dry, dry, and pass through a good place. If it is in a tidal environment, it is feared that there will be reactions such as hydrolysis, which will cause the substance to be damaged. For example, the moisture contained in the tidal air may interact with its active radical phase, change its chemical properties, and lose its original properties.
Second, the control of the degree also needs to be controlled. High-temperature environments can promote the rate of transformation and reaction, and even lead to uncontrollable reactions. Therefore, avoid direct sunlight and do not expose to high temperatures. If the degree of preservation is high, the compound may decompose or polymerize, which is not what we want.
Furthermore, on the way, it is necessary to prevent it from being shaken or collided. This external force may break its molecules, or cause local reactions. And it is necessary to isolate other chemical products. Due to the incompatibility of different materials, or incompatible characteristics, once connected, it may cause severe reactions and endanger the safety of the product.
In addition, the solid density of the package cannot be ignored. A well-sealed package can block the drying of external air, moisture, etc., and keep the material safe during storage and storage. If the package is intact, external factors are easily intrusive, causing the product to be damaged.
Therefore, the storage of 4 + -1-methoxy-2-benzyl ether should be done with caution and attention should be paid to the safety of the product.
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