Linshang Chemical
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2-(3-Chloropropoxy)-1-Methoxy-4-Nitrobenzene
Linshang Chemical
|
HS Code |
325293 |
| Chemical Formula | C10H10ClNO5 |
| Molecular Weight | 261.64 |
As an accredited 2-(3-Chloropropoxy)-1-Methoxy-4-Nitrobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 500g of 2-(3 - chloropropoxy)-1-methoxy-4-nitrobenzene in sealed chemical - grade containers. |
| Storage | Store 2-(3 - chloropropoxy)-1 - methoxy - 4 - nitrobenzene in a cool, dry, well - ventilated area. Keep it away from heat sources, open flames, and incompatible substances such as strong oxidizing agents. Store in a tightly closed container to prevent moisture and air exposure, which could potentially lead to degradation or reaction. |
| Shipping | 2-(3 - Chloropropoxy)-1 - methoxy - 4 - nitrobenzene is shipped in accordance with chemical transport regulations. It's packaged securely in appropriate containers to prevent leakage during transit to ensure safety. |
Competitive 2-(3-Chloropropoxy)-1-Methoxy-4-Nitrobenzene prices that fit your budget—flexible terms and customized quotes for every order.
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As a leading 2-(3-Chloropropoxy)-1-Methoxy-4-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- (3-chloropropoxy) -1-methoxy-4-nitrobenzene?
2-% (3-chloropropoxy) -1-methoxy-4-nitrobenzene, this is an organic compound. It has a wide range of uses and is of great significance in many fields.
In the field of pharmaceutical synthesis, it often acts as a key intermediate. Due to the specific chemical structure of this compound, it can participate in a series of chemical reactions to construct more complex drug molecular structures. By chemically modifying and transforming it, drugs with specific pharmacological activities can be prepared for the treatment of diseases.
In the field of materials science, it also shows unique value. or can be used as a raw material for the synthesis of special performance polymer materials. After rational design and polymerization reaction, the resulting polymer material can have good thermal stability, electrical properties or optical properties, etc., and can be applied in electronic devices, optical materials, etc.
In the research and development of pesticides, it also has its place. New pesticides can be developed based on this compound. Because of its chemical properties or can inhibit or kill specific pests or bacteria, it provides assistance for pest control in agricultural production.
In summary, 2% (3-chloropropoxy) -1-methoxy-4-nitrobenzene is an important basic substance in many fields such as medicine, materials, and pesticides due to its special chemical structure, and plays a key role in promoting the development of related fields.
In the field of pharmaceutical synthesis, it often acts as a key intermediate. Due to the specific chemical structure of this compound, it can participate in a series of chemical reactions to construct more complex drug molecular structures. By chemically modifying and transforming it, drugs with specific pharmacological activities can be prepared for the treatment of diseases.
In the field of materials science, it also shows unique value. or can be used as a raw material for the synthesis of special performance polymer materials. After rational design and polymerization reaction, the resulting polymer material can have good thermal stability, electrical properties or optical properties, etc., and can be applied in electronic devices, optical materials, etc.
In the research and development of pesticides, it also has its place. New pesticides can be developed based on this compound. Because of its chemical properties or can inhibit or kill specific pests or bacteria, it provides assistance for pest control in agricultural production.
In summary, 2% (3-chloropropoxy) -1-methoxy-4-nitrobenzene is an important basic substance in many fields such as medicine, materials, and pesticides due to its special chemical structure, and plays a key role in promoting the development of related fields.
What are the physical properties of 2- (3-chloropropoxy) -1-methoxy-4-nitrobenzene
2-% 283 - chloropropoxy% 29 - 1 - methoxy - 4 - nitrobenzene, this is an organic compound with unique physical properties. It is mostly solid at room temperature, and it has a certain melting point and boiling point due to the force between molecules. The melting point, or due to the characteristics of the molecular structure, makes it gradually change from solid to liquid at a specific temperature. The molecule contains different groups such as chlorine, methoxy, and nitro. The electronegativity of the chlorine atom is large, which will affect the polarity of the molecule and also play a role in the melting point.
When talking about the boiling point, the boiling point between molecules is within a certain range due to the effect of Van der Waals force or hydrogen bonds. The presence of nitro groups enhances the polarity of the molecule or increases the boiling point. And the density of this compound is greater than that of water, due to the influence of its molecular structure and relative molecular mass. If it is placed in water, it will sink to the bottom of the water.
In terms of solubility, due to the presence of methoxy, nitro and other groups, it has good solubility in organic solvents, such as ethanol, ether, etc. The lipophilicity of methoxy groups makes molecules have good affinity with organic solvents. In water, although nitro and other polar groups have a certain hydrophilicity, the hydrophobicity of the overall molecular structure results in limited solubility in water.
In appearance, it may be white to light yellow solid, and the color may vary depending on impurities and synthesis methods. In conclusion, the physical properties of 2-% 283-chloropropoxy% 29-1-methoxy-4-nitrobenzene are determined by its molecular structure, and different groups interact to create its melting point, boiling point, density, solubility and appearance.
When talking about the boiling point, the boiling point between molecules is within a certain range due to the effect of Van der Waals force or hydrogen bonds. The presence of nitro groups enhances the polarity of the molecule or increases the boiling point. And the density of this compound is greater than that of water, due to the influence of its molecular structure and relative molecular mass. If it is placed in water, it will sink to the bottom of the water.
In terms of solubility, due to the presence of methoxy, nitro and other groups, it has good solubility in organic solvents, such as ethanol, ether, etc. The lipophilicity of methoxy groups makes molecules have good affinity with organic solvents. In water, although nitro and other polar groups have a certain hydrophilicity, the hydrophobicity of the overall molecular structure results in limited solubility in water.
In appearance, it may be white to light yellow solid, and the color may vary depending on impurities and synthesis methods. In conclusion, the physical properties of 2-% 283-chloropropoxy% 29-1-methoxy-4-nitrobenzene are determined by its molecular structure, and different groups interact to create its melting point, boiling point, density, solubility and appearance.
What are the chemical properties of 2- (3-chloropropoxy) -1-methoxy-4-nitrobenzene?
2-% 283 - chloropropoxy% 29 - 1 - methoxy - 4 - nitrobenzene is also an organic compound. It has unique chemical properties, which are related to the reactivity and stability.
In terms of reactivity, the nitro group in the molecule is a strong electron-absorbing group, which reduces the electron cloud density of the benzene ring and weakens the electrophilic substitution activity of the benzene ring. However, in the nucleophilic substitution reaction, the nitro group can enhance the activity of the benzene ring ortho and para-position. In the case of nucleophilic reagents, the substitution reaction of the nitro ortho and para-position may occur under suitable conditions.
Its alkoxy moiety, such as methoxy and 3-chloropropoxy, also has specific roles. Methoxy is the power supply group, which has an impact on the electron cloud distribution of the benzene ring, and can change the activity check point of the benzene ring to a certain extent. In the 3-chloropropoxy group, the chlorine atom is active and can participate in the substitution reaction, or can react with nucleophiles, causing the carbon-chlorine bond to break and introducing new groups.
In terms of stability, the atoms in the molecular structure are connected by covalent bonds to form a stable structure. However, the presence of nitro groups makes the molecule have a certain polarity. In specific environments, such as high temperature and strong acid-base conditions, it may affect its stability and cause reactions such as decomposition.
In terms of solubility, due to the fact that the molecule contains polar groups nitro, methoxy, and non-polar benzene rings and alkyl moieties, it may have a certain solubility in polar organic solvents such as alcohols and ketones, and its solubility in non-polar solvents such as alkanes may be limited.
In summary, the chemical properties of 2-% 283-chloropropoxy% 29-1-methoxy-4-nitrobenzene are determined by the coordination of various groups in its molecular structure, and exhibit diverse characteristics in different reactions and environments.
In terms of reactivity, the nitro group in the molecule is a strong electron-absorbing group, which reduces the electron cloud density of the benzene ring and weakens the electrophilic substitution activity of the benzene ring. However, in the nucleophilic substitution reaction, the nitro group can enhance the activity of the benzene ring ortho and para-position. In the case of nucleophilic reagents, the substitution reaction of the nitro ortho and para-position may occur under suitable conditions.
Its alkoxy moiety, such as methoxy and 3-chloropropoxy, also has specific roles. Methoxy is the power supply group, which has an impact on the electron cloud distribution of the benzene ring, and can change the activity check point of the benzene ring to a certain extent. In the 3-chloropropoxy group, the chlorine atom is active and can participate in the substitution reaction, or can react with nucleophiles, causing the carbon-chlorine bond to break and introducing new groups.
In terms of stability, the atoms in the molecular structure are connected by covalent bonds to form a stable structure. However, the presence of nitro groups makes the molecule have a certain polarity. In specific environments, such as high temperature and strong acid-base conditions, it may affect its stability and cause reactions such as decomposition.
In terms of solubility, due to the fact that the molecule contains polar groups nitro, methoxy, and non-polar benzene rings and alkyl moieties, it may have a certain solubility in polar organic solvents such as alcohols and ketones, and its solubility in non-polar solvents such as alkanes may be limited.
In summary, the chemical properties of 2-% 283-chloropropoxy% 29-1-methoxy-4-nitrobenzene are determined by the coordination of various groups in its molecular structure, and exhibit diverse characteristics in different reactions and environments.
What is the synthesis method of 2- (3-chloropropoxy) -1-methoxy-4-nitrobenzene
To prepare 2 - (3 - chloropropoxy) - 1 - methoxy - 4 - nitrobenzene, the following method can be used.
First take 1 - methoxy - 4 - nitrobenzene as the starting material. In the structure of this substance, the localization effect of methoxy group and nitro group makes the activity of specific positions on the benzene ring different. Under appropriate reaction conditions, 1 - methoxy - 4 - nitrobenzene is reacted with 3 - chloro - 1 - propanol. This reaction requires the selection of suitable catalysts, such as some Lewis acid catalysts with specific active centers, which can promote the nucleophilic substitution reaction between the two. During the reaction, the oxygen atom of the hydroxyl group in 3-chloro-1-propanol has nucleophilicity and will attack the carbon atom on the 1-methoxy-4-nitrophenyl ring that is enhanced by the positioning effect of methoxy and nitro groups. At the same time, the chloride ions leave to form the target product 2- (3-chloropropoxy) -1-methoxy-4-nitrobenzene. The choice of solvent for the
reaction system is also crucial. Polar aprotic solvents, such as N, N-dimethylformamide (DMF) or dimethyl sulfoxide (DMSO), are required. Such solvents can not only dissolve the reactants, but also facilitate the nucleophilic substitution reaction. They can stabilize the reaction intermediates, reduce the activation energy of the reaction, and promote the smooth progress of the reaction towards the formation of the target product. The reaction temperature needs to be carefully controlled, generally controlled in the moderate temperature range. If the temperature is too high, it may trigger side reactions and reduce the purity of the product; if the temperature is too low, the reaction rate is too slow and the time is too long. During the reaction process, the reaction process can be monitored by thin layer chromatography (TLC) and other means. When the raw material point basically disappears, it indicates that the reaction has reached the expected level. After the reaction, the pure 2 - (3-chloropropoxy) - 1 - methoxy - 4 - nitrobenzene product can be obtained through post-treatment processes such as extraction, washing, drying, column chromatography, etc.
First take 1 - methoxy - 4 - nitrobenzene as the starting material. In the structure of this substance, the localization effect of methoxy group and nitro group makes the activity of specific positions on the benzene ring different. Under appropriate reaction conditions, 1 - methoxy - 4 - nitrobenzene is reacted with 3 - chloro - 1 - propanol. This reaction requires the selection of suitable catalysts, such as some Lewis acid catalysts with specific active centers, which can promote the nucleophilic substitution reaction between the two. During the reaction, the oxygen atom of the hydroxyl group in 3-chloro-1-propanol has nucleophilicity and will attack the carbon atom on the 1-methoxy-4-nitrophenyl ring that is enhanced by the positioning effect of methoxy and nitro groups. At the same time, the chloride ions leave to form the target product 2- (3-chloropropoxy) -1-methoxy-4-nitrobenzene. The choice of solvent for the
reaction system is also crucial. Polar aprotic solvents, such as N, N-dimethylformamide (DMF) or dimethyl sulfoxide (DMSO), are required. Such solvents can not only dissolve the reactants, but also facilitate the nucleophilic substitution reaction. They can stabilize the reaction intermediates, reduce the activation energy of the reaction, and promote the smooth progress of the reaction towards the formation of the target product. The reaction temperature needs to be carefully controlled, generally controlled in the moderate temperature range. If the temperature is too high, it may trigger side reactions and reduce the purity of the product; if the temperature is too low, the reaction rate is too slow and the time is too long. During the reaction process, the reaction process can be monitored by thin layer chromatography (TLC) and other means. When the raw material point basically disappears, it indicates that the reaction has reached the expected level. After the reaction, the pure 2 - (3-chloropropoxy) - 1 - methoxy - 4 - nitrobenzene product can be obtained through post-treatment processes such as extraction, washing, drying, column chromatography, etc.
2- (3-chloropropoxy) -1-methoxy-4-nitrobenzene what to pay attention to when storing and transporting
2-% 283-chloropropoxy% 29-1-methoxy-4-nitrobenzene is also an organic compound. When storing and transporting it, many matters must be paid attention to.
First words storage, this compound should be placed in a cool, dry and well-ventilated place. Because the cool environment can avoid chemical changes caused by excessive temperature, the dry place can prevent it from being damp and affect the purity and stability, and good ventilation can prevent the accumulation of harmful gases. And be sure to keep away from fire and heat sources, because it may be flammable or dangerous due to heat interaction.
Furthermore, it should be stored separately from oxidizing agents, acids, bases, etc. Due to its chemical structure, coexistence with such substances can easily cause chemical reactions, or cause disasters such as combustion and explosion. At the same time, the storage place should have suitable materials to contain leaks, so as to prevent accidents, and can respond in time to reduce damage hazards.
As for transportation, it is necessary to ensure that the packaging is complete and secure before transportation. The packaging must be able to withstand a certain amount of external force, so as not to cause leakage due to damage during transportation. During transportation, the relevant regulations should also be followed. The speed of the vehicle should not be too fast to prevent the bumps and vibrations from being too severe, so as to avoid damage to the packaging. The transportation vehicle should be equipped with the corresponding variety and quantity of fire-fighting equipment and leakage emergency treatment equipment. In case of leakage, measures can be taken immediately. Escort personnel must be familiar with the nature of the goods being transported and the emergency response methods, and carefully guard the journey to ensure the safety of transportation.
First words storage, this compound should be placed in a cool, dry and well-ventilated place. Because the cool environment can avoid chemical changes caused by excessive temperature, the dry place can prevent it from being damp and affect the purity and stability, and good ventilation can prevent the accumulation of harmful gases. And be sure to keep away from fire and heat sources, because it may be flammable or dangerous due to heat interaction.
Furthermore, it should be stored separately from oxidizing agents, acids, bases, etc. Due to its chemical structure, coexistence with such substances can easily cause chemical reactions, or cause disasters such as combustion and explosion. At the same time, the storage place should have suitable materials to contain leaks, so as to prevent accidents, and can respond in time to reduce damage hazards.
As for transportation, it is necessary to ensure that the packaging is complete and secure before transportation. The packaging must be able to withstand a certain amount of external force, so as not to cause leakage due to damage during transportation. During transportation, the relevant regulations should also be followed. The speed of the vehicle should not be too fast to prevent the bumps and vibrations from being too severe, so as to avoid damage to the packaging. The transportation vehicle should be equipped with the corresponding variety and quantity of fire-fighting equipment and leakage emergency treatment equipment. In case of leakage, measures can be taken immediately. Escort personnel must be familiar with the nature of the goods being transported and the emergency response methods, and carefully guard the journey to ensure the safety of transportation.
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